Citations (200)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (12)
Fereshteh Bagheri, Zeinab Miresmaeili, Mousa Ahmadpour-kacho & Zohreh Ziatabar Ahmadi. (2023) Relationship between risk factors of hearing loss and the results of otoacoustic emission in newborns. Hearing, Balance and Communication 21:2, pages 82-87.
Read now
Read now
Azam Pourahmadiyan, Paria Alipour, Neda Golchin & Mohammad Amin Tabatabaiefar. (2022) Next-generation sequencing reveals a novel pathogenic variant in the ATM gene. International Journal of Neuroscience 132:6, pages 558-562.
Read now
Read now
Azam Pourahmadiyan, Morteza Heidari, Hossein Shojaaldini Ardakani, Shahab Noorian & Shahram Savad. (2021) A novel pathogenic variant of BRAT1 gene causes rigidity and multifocal seizure syndrome, lethal neonatal. International Journal of Neuroscience 131:9, pages 875-878.
Read now
Read now
Hassan Mansouritorghabeh. (2021) Consanguineous marriage and rare bleeding disorders. Expert Review of Hematology 14:5, pages 467-472.
Read now
Read now
Masoumeh Falah, Massoud Houshmand, Maryam Balali, Alimohamad Asghari, Zohreh Bagher, Rafieh Alizadeh & Mohammad Farhadi. (2020) Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews. Fetal and Pediatric Pathology 39:1, pages 1-12.
Read now
Read now
Azam Pourahmadiyan, Paria Alipour, Najmeh Fattahi, Mahbubeh Kasiri, Fateme Rezaeian, Afsaneh Taghipour-Sheshdeh, Javad Mohammadi-Asl, Mohammad Amin Tabatabaiefar & Morteza Hashemzadeh Chaleshtori. (2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. International Journal of Audiology 58:10, pages 628-634.
Read now
Read now
Mohammad Naderan, Mohammad Taher Rajabi, Parviz Zarrinbakhsh, Morteza Naderan & Anahita Bakhshi. (2016) Association between Family History and Keratoconus Severity. Current Eye Research 41:11, pages 1414-1418.
Read now
Read now
Marzieh Mojbafan, Yalda Nilipour, Seyed Hasan Tonekaboni, Javad Tavakkoly-Bazzaz & Sirous Zeinali. (2016) A novel mutation in alpha sarcoglycan gene in an Iranian family with limb girdle muscular dystrophy 2D. Neurological Research 38:3, pages 220-223.
Read now
Read now
Marzieh Mojbafan, Yalda Nilipour, Seyed Hasan Tonekaboni, Samira Dabbagh Bagheri, Hamideh Bagherian, Zohreh Sharifi, Zahra Zeinali, Javad Tavakkoly-Bazzaz & Sirous Zeinali. (2016) A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping. Journal of Neurogenetics 30:1, pages 1-4.
Read now
Read now
Elham Davoudi-Dehaghani, Mohammad-Sadegh Fallah, Javad Tavakkoly-Bazzaz, Hamideh Bagherian & Sirous Zeinali. (2015) Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing. Acta Oto-Laryngologica 135:2, pages 125-129.
Read now
Read now
Ali Bidari, Banafsheh Ghavidel-Parsa, Hossein Najmabadi, Elham Talachian, Majid Haghighat-Shoar, Behrooz Broumand & Babak Ghalehbaghi. (2010) Common MEFV mutation analysis in 36 Iranian patients with familial Mediterranean fever: clinical and demographic significance. Modern Rheumatology 20:6, pages 566-572.
Read now
Read now
Hessom Razavi, Hannah Kuper, Farhad Rezvan, Khatere Amelie, Hassan Mahboobi-Pur, Mohammad Reza Oladi, Mohammad Muhit & Hassan Hashemi. (2010) Prevalence and Causes of Severe Visual Impairment and Blindness Among Children in the Lorestan Province of Iran, Using the Key Informant Method. Ophthalmic Epidemiology 17:2, pages 95-102.
Read now
Read now
Articles from other publishers (188)
Anahita Khodabakhshi-Koolaee & Zahra Amoogholi. (2022) The psychosocial experiences of girls with visual impairment about the ideal spouse and marriage. British Journal of Visual Impairment 42:2, pages 312-324.
Crossref
Crossref
Saeed Ghasemi, Marzieh Mojbafan, Saeed Talebi, Nakysa Hooman & Rozita Hoseini. (2024) Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population. Molecular Genetics & Genomic Medicine 12:4.
Crossref
Crossref
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad & Hossein Najmabadi. (2024) Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population. npj Genomic Medicine 9:1.
Crossref
Crossref
Abdullah M Khayat, Balsam Ghazi Alshareef, Sara F Alharbi, Mohammed Mansour AlZahrani, Bashaer Abdulwahab Alshangity & Noha Farouk Tashkandi. (2024) Consanguineous Marriage and Its Association With Genetic Disorders in Saudi Arabia: A Review. Cureus.
Crossref
Crossref
Teymoor Khosravi, Karim Naghipoor, Fatemeh Vaghefi, Ali Mohammad Falahati & Morteza Oladnabi. (2024) In silico analysis of mutation spectrum of Ehlers–Danlos, osteogenesis imperfecta, and cutis laxa overlapping phenotypes in Iranian population. Egyptian Journal of Medical Human Genetics 25:1.
Crossref
Crossref
Shenali A. Amaratunga, Tara Hussein Tayeb, Rozhan N. Muhamad Sediq, Fareda K. Hama Salih, Petra Dusatkova, Matthew N. Wakeling, Elisa De Franco, Stepanka Pruhova & Jan Lebl. (2023) Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq. Diabetologia 67:1, pages 113-123.
Crossref
Crossref
Jonathan Spoor, Hamid Farajifard, Mahsa Keshavarz-FathiNima Rezaei. (2023) Historical Cohort of Severe Congenital Neutropenia in Iran: Clinical Course, Laboratory Evaluation, Treatment, and Survival. Journal of Pediatric Hematology/Oncology 45:5, pages e643-e649.
Crossref
Crossref
Farzaneh Abbasi, Saideh Abdolahpour, Reihaneh Mohsenipour, Ali Rabbani, Ali Talea, Ali Mohebbi & Maryam Khazdouz. (2023) Inborn Errors of Metabolism in Iran: First Report from Iran Metabolic Registry. Iranian Journal of Pediatrics 33:3.
Crossref
Crossref
Nima Farshidfar, Shabnam Ajami, Sarina Sahmeddini, Ali Goli & Hamid Reza Foroutan. (2023) Epidemiological and Spatiotemporal Descriptive Analysis of Patients with Nonsyndromic Cleft Lip and/or Palate: A 12-Year Retrospective Study in Southern Iran. BioMed Research International 2023, pages 1-19.
Crossref
Crossref
Vahid Mansouri, Morteza Heidari, Maryam Bemanalizadeh, Reza Azizimalamiri, Shahriar Nafissi, Masood Ghahvechi Akbari, Mohammad Barzegar, Ali Reza Moayedi, Reza Shervin Badv, Mahmood Mohamadi, Ali Reza Tavasoli, Susan Amirsalari, Ali Khajeh, Soroor Inaloo, Farzad Fatehi, Sareh Hosseinpour, Meisam Babaei, Seyed Ahmad Hosseini, Seyyed Mohammad Mahdi Hosseiny, Afshin Fayyazi, Firoozeh Hosseini, Mehran Beiraghi Toosi, Nahid Khosroshahi, Homa Ghabeli, Habibeh Nejad Biglari, Simin Khayatzadeh Kakhki, Seyed Hossein Mirlohi, Elham Bidabadi, Bahram Mohammadi, Abdolmajid Omrani, Mostafa Sedighi, Mohammad Vafaee-Shahi, Maryam Rasulinezhad, Seyyed Mohamad Hoseini, Mojtaba Movahedinia, Zahra Rezaei, Parviz Karimi, Hossein Farshadmoghadam, Saeed Anvari, Omid Yaghini, Jafar Nasiri, Gholamreza Zamani & Mahmoud Reza Ashrafi. (2023) The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy. Journal of Neuromuscular Diseases 10:2, pages 211-225.
Crossref
Crossref
Mostafa Feghhi, Mohammad Ali Moghimi, Ali Kasiri & Fereydoun Farrahi. (2023) Relative frequency of inherited retinal disorders in Khuzestan province, southern Iran. Journal of Advanced Pharmacy Education and Research 13:1, pages 42-45.
Crossref
Crossref
Amir Nik, Najmeh Ahangari, Paria Najarzadeh Torbati, Reza Boostani & Ehsan Ghayoor Karimiani. (2022) Chloride Channel Mutations Leading to Congenital Myotonia. Cureus.
Crossref
Crossref
İsmet KOÇ. (2022) Türkiye’de akraba evliliklerinin yaygınlığının değişimi ve dirençli grupların belirlenmesi: 2018 Türkiye Nüfus ve Sağlık Araştırması’ndan evlilik kuşaklarına göre analizlerDetermining the changes in the prevalence of consanguineous marriages and resistant Groups in Turkey: Analyses by marriage cohorts from the 2018 Turkish Demographic and Health Survey. Türkiye Halk Sağlığı Dergisi 20:3, pages 423-438.
Crossref
Crossref
Mostafa Saadat. (2022) Morbidity and mortality of COVID-19 negatively associated with the frequency of consanguineous marriages, an ecologic study. Egyptian Journal of Medical Human Genetics 23:1.
Crossref
Crossref
Tohid Ghasemnejad, Mahmoud Shekari Khaniani, Jafar Nouri Nojadeh & Sima Mansoori Derakhshan. (2022) A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case. BMC Medical Genomics 15:1.
Crossref
Crossref
Zahra Salehi, Amir Almasi-Hashiani, Mohammad Ali Sahraian, Fereshteh Ashtari, Seyed Mohammad Baghbanian, Nazanin Razazian, Abdorreza Naser Moghadasi, Asghar Bayati, Amir Reza Azimi, Nahid Beladimoghadam, Mohammad Hossein Harirchian, Maryam Poursadeghfard, Samira Navardi, Reza Shirkoohi, Hora Heidari, Mehran Ghaffari & Sharareh Eskandarieh. (2022) Epidemiology of familial multiple sclerosis in Iran: a national registry-based study. BMC Neurology 22:1.
Crossref
Crossref
Fardin Faraji, Pegah Mohaghegh & Afsoon Talaie. (2022) Epidemiology of familial multiple sclerosis and its comparison to sporadic form in Markazi Province, Iran. Multiple Sclerosis and Related Disorders 68, pages 104231.
Crossref
Crossref
Soraya Hadjali‐Saichi, Philippe de Mazancourt, Jacqueline Tapon‐Bretaudière, Tristan Mirault, Kahina Guenounou, Issam Frigaa, Anne‐Marie Fischer, Ouerdia Chafa & Dominique Helley. (2022) Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria. Haemophilia 28:5, pages 822-831.
Crossref
Crossref
Leman Damla Kotan. (2022) Comparative Analyses of Turkish Variome and Widely Used Genomic Variation Databases for the Evaluation of Rare Sequence Variants in Turkish Individuals: Idiopathic Hypogonadotropic Hypogonadism as a Disease Model. Journal of Clinical Research in Pediatric Endocrinology 14:3, pages 293-301.
Crossref
Crossref
Juan Antonio Gili, Jorge Santiago López‐Camelo, Wendy N. Nembhard, Marian Bakker, Hermien E. K. de Walle, Erin B. Stallings, Vijaya Kancherla, Paolo Contiero, Saeed Dastgiri, Marcia L. Feldkamp, Amy Nance, Miriam Gatt, Laura Martínez, María Aurora Canessa, Boris Groisman, Paula Hurtado‐Villa, Karin Källén, Danielle Landau, Nathalie Lelong, Margery Morgan, Jazmín Arteaga‐Vázquez, Anna Pierini, Anke Rissmann, Antonin Sipek, Elena Szabova, Wladimir Wertelecki, Ignacio Zarante, Mark A. Canfield & Pierpaolo Mastroiacovo. (2022)
Analysis of early neonatal case fatality rate among newborns with congenital hydrocephalus, a 2000–2014
multi‐country registry‐based
study
. Birth Defects Research 114:12, pages 631-644.
Crossref
Crossref
Amir Samii, Mahshaad Norouzi, Abbas Ahmadi & Akbar Dorgalaleh. (2022) Gastrointestinal Bleeding in Congenital Bleeding Disorders. Seminars in Thrombosis and Hemostasis 48:05, pages 529-541.
Crossref
Crossref
Mojgan Babanejad, Maryam Beheshtian, Fereshteh Jamshidi, Marzieh Mohseni, Kevin T. Booth, Kimia Kahrizi & Hossein Najmabadi. (2022) Genetic etiology of hearing loss in Iran. Human Genetics 141:3-4, pages 623-631.
Crossref
Crossref
Samaneh Asgari, Davood Khalili, Yadollah Mehrabi & Farzad Hadaegh. (2021) Letter to the Editor Regarding “Nationwide Prevalence of Diabetes and Prediabetes and Associated Risk Factors Among Iranian Adults: Analysis of Data from PERSIAN Cohort Study”. Diabetes Therapy 13:1, pages 217-219.
Crossref
Crossref
Fatemeh Bitarafan, Mehrnoosh Khodaeian, Elham Amjadi Sardehaei, Fatemeh Zahra Darvishi, Navid Almadani, Yalda Nilipour & Masoud Garshasbi. (2021) Identification of a novel MICU1 nonsense variant causes myopathy with extrapyramidal signs in an Iranian consanguineous family. Molecular and Cellular Pediatrics 8:1.
Crossref
Crossref
Fatemeh Sadat Mahdavi, Mohammad Keramatipour, Sarina Ansari, Samin Sharafian, Arezou Karamzade & Marzieh Tavakol. (2021) X-linked SCID with a rare mutation. Allergy, Asthma & Clinical Immunology 17:1.
Crossref
Crossref
Reza Alibakhshi, Aboozar Mohammadi, Sahand Khamooshian, Mohsen Kazeminia & Keivan Moradi. (2021)
CFTR
gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review
. Pediatric Pulmonology 56:12, pages 3644-3656.
Crossref
Crossref
Mona Habibi & Shaghayegh Vahdat. (2021) Evaluation of the Correlation between Socioeconomic Factors and Pediatric Cleft Lip and Palate. Modern Medical Laboratory Journal 4:2, pages 40-49.
Crossref
Crossref
Zohreh Sharifi, Mohammad Taheri, Mohammad-Sadegh Fallah, Maryam Abiri, Fatemeh Golnabi, Hamideh Bagherian, Razieh Zeinali, Hossein Farahzadi, Marjan Alborji, Pardis Ghazizadeh Tehrani, Masoume Amini, Sadaf Asnavandi, Mehrdad Hashemi, Flora Forouzesh & Sirous Zeinali. (2021) Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran. Journal of Molecular Neuroscience 71:11, pages 2281-2298.
Crossref
Crossref
Ehsan Abbaspour Rodbaneh, Mohammad Panahi, Bahareh Rahimi, Haleh Mokabber, Reza Farajollahi & Behzad Davarnia. (2021) GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran. Journal of Clinical Laboratory Analysis 35:11.
Crossref
Crossref
Nasrin GHARIBSHAHI, Hazhir JAVAHERIZADEH, Zahra Nazari KHORASGANI & Masoud MAHDAVINIA. (2021) RELATIONSHIP BETWEEN LEAD AND CADMIUM LEVELS IN BLOOD AND REFRACTORY CHRONIC CONSTIPATION AMONG IRANIAN CHILDREN. Arquivos de Gastroenterologia 58:3, pages 329-336.
Crossref
Crossref
Parisa Amirifar, Mohammad Reza Ranjouri, Salar Pashangzadeh, Martin Lavin, Reza Yazdani, Tannaz Moeini Shad, Mahya Mehrmohamadi, Fereshte Salami, Samaneh Delavari, Soraya Moamer, Asghar Aghamohammadi, Seyed Mohammad Akrami & Hassan Abolhassani. (2021)
The spectrum of
ATM
gene mutations in Iranian patients with ataxia‐telangiectasia
. Pediatric Allergy and Immunology 32:6, pages 1316-1326.
Crossref
Crossref
Hossein Jafari Khamirani, Sina Zoghi, Fatemeh Faghihi, Seyed Alireza Dastgheib, Hamidreza Hassanipour, Seyed Mohammad Bagher Tabei, Sanaz Mohammadi, Marjan Masoudi, Shiva Poorang, Elham Ehsani & Mehdi Dianatpour. (2021) Phenotype of ST3GAL3 deficient patients: A case and review of the literature. European Journal of Medical Genetics 64:8, pages 104250.
Crossref
Crossref
Ladan Mehran, Fereidoun Azizi, Pouria Mousapour, Leila Cheraghi, Shahin Yarahmadi, Golshan Amirshekari & Davood Khalili. (2021) Development of a risk prediction model for early discrimination between permanent and transient congenital hypothyroidism. Endocrine 73:2, pages 374-383.
Crossref
Crossref
Zahra Salehi, Mohammad Keramatipour, Saeed Talebi, Seyed Shahriar Arab, Abdorreza Naser Moghadasi, Mohammad Ali Sahraian & Maryam Izad. (2021) Exome sequencing reveals novel rare variants in Iranian familial multiple sclerosis: The importance of POLD2 in the disease pathogenesis. Genomics 113:4, pages 2645-2655.
Crossref
Crossref
Taraneh Ghaffari, Naser Mirhosseini Motlagh, Abdolreza Daraei, Majid Tafrihi, Mehrdad Saravi & Davood Sabour. (2021) Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients. Functional & Integrative Genomics 21:3-4, pages 331-340.
Crossref
Crossref
Soraya Bakhshani. (2021) Consanguineous Marriage and the Risk of Parents Having Children with Cleft Lip and Palate. International Journal of High Risk Behaviors and Addiction 10:2.
Crossref
Crossref
Reza Alibakhshi, Aboozar Mohammadi, Nader Salari, Sahand Khamooshian, Mohsen Kazeminia & Keivan Moradi. (2021) Spectrum of PAH gene mutations in 1547 phenylketonuria patients from Iran: a comprehensive systematic review. Metabolic Brain Disease 36:5, pages 767-780.
Crossref
Crossref
Zahra Beyzaei, Fatih Ezgu, Bita Geramizadeh, Mohammad Hadi Imanieh, Mahmood Haghighat, Seyed Mohsen Dehghani, Naser Honar, Mojgan Zahmatkeshan, Amirreza Jassbi, Marjan Mahboubifar & Alireza Alborzi. (2021) Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing. Scientific Reports 11:1.
Crossref
Crossref
Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad & Hossein Najmabadi. (2021) Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities. Scientific Reports 11:1.
Crossref
Crossref
Mathieu Quinodoz, Virginie G. Peter, Nicola Bedoni, Béryl Royer Bertrand, Katarina Cisarova, Arash Salmaninejad, Neda Sepahi, Raquel Rodrigues, Mehran Piran, Majid Mojarrad, Alireza Pasdar, Ali Ghanbari Asad, Ana Berta Sousa, Luisa Coutinho Santos, Andrea Superti-Furga & Carlo Rivolta. (2021) AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data. Nature Communications 12:1.
Crossref
Crossref
Ameer Kakaje, Mohammad Marwan Alhalabi, Ayham Ghareeb, Bahjat Karam, Bassam Mansour, Bayan Zahra & Othman Hamdan. (2020) Interactions of Consanguinity and Number of Siblings with Childhood Acute Lymphoblastic Leukemia. BioMed Research International 2020, pages 1-11.
Crossref
Crossref
Behzad Cheshmi, Zahra Jafari, Mohammad Ali Naseri & Heidar Ali Davari. (2020) Assessment of the correlation between various risk factors and orofacial cleft disorder spectrum: a retrospective case-control study. Maxillofacial Plastic and Reconstructive Surgery 42:1.
Crossref
Crossref
Maryam Eghbali, Maryam Abiri, Saeed Talebi, Zahra Noroozi, Marjan Shakiba, Parastoo Rostami, Hosein Alimadadi, Mehri Najafi, Fatemeh Yazarlou, Ali Rabbani & Mohammad Hossein Modarressi. (2020) Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b). Orphanet Journal of Rare Diseases 15:1.
Crossref
Crossref
Parham Habibzadeh, Zahra Tabatabaei, Mohammad Ali Farazi Fard, Laila Jamali, Aazam Hafizi, Pooneh Nikuei, Leila Salarian, Mohammad Hossein Nasr Esfahani, Zahra Anvar & Mohammad Ali Faghihi. (2020) Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene. BMC Medical Genetics 21:1.
Crossref
Crossref
Marzia Menegatti & Roberta Palla. (2020) Clinical and laboratory diagnosis of rare coagulation disorders (RCDs). Thrombosis Research 196, pages 603-608.
Crossref
Crossref
Juan F. Gamella. (2019)
Consanguineous marriages among Andalusian
Gitanos/Calé
: a genealogical analysis (1925–2006)
. Journal of Biosocial Science 52:6, pages 809-831.
Crossref
Crossref
Yu Qiang Soh, Viridiana Kocaba, Jayne S. Weiss, Ula V. Jurkunas, Shigeru Kinoshita, Anthony J. Aldave & Jodhbir S. Mehta. (2020) Corneal dystrophies. Nature Reviews Disease Primers 6:1.
Crossref
Crossref
Parisa Atefvahid, Mohammad Hossein Modarressi, Ashraf Aleyasin & Zahra Noormohammadi. (2020) Copy number variations in miscarriage products and their relationship with consanguinity and recurrent miscarriage in individuals with normal karyotypes. Molecular and Cellular Probes 51, pages 101526.
Crossref
Crossref
Hassan Vahidnezhad, Leila Youssefian, Soheila Sotoudeh, Lu Liu, Alyson Guy, Patricia A. Lovell, Ariana Kariminejad, Sirous Zeinali, John A. McGrath & Jouni Uitto. (2020) Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica. Human Mutation 41:5, pages 906-912.
Crossref
Crossref
Shahnaz Naghashi, Mandana Rafeey, Morteza Ghojazadeh, Zeinab Nikniaz, Saeid Aslanabadi & Maryam Shoaran. (2020) Biliary Atresia in Northwest Iran: Epidemiologic Features and Long-Term Outcome. Iranian Journal of Pediatrics 30:2.
Crossref
Crossref
Ameni Kdissa, Klaus Brusgaard, Mahdi Ksiaa, Lamia Golli, Olfa Hallara, Lilian Bomme Ousager, Wiem Manoubi, Rihab Ben Seghaier, Labiba Adala, Yosra Halleb, Ali Saad, Fahmi Hmila & Moez Gribaa. (2020) c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis. Cancer Genetics 240, pages 45-53.
Crossref
Crossref
Mohammad Reza Pourreza, Maryam Sobhani, Azadeh Rahimi, Mehdi Aramideh, Abdol-Mohammad Kajbafzadeh, Mohammad Reza Noori-Daloii & Mohammad Amin Tabatabaiefar. (2019) Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family. Acta Diabetologica 57:1, pages 81-87.
Crossref
Crossref
Shilpa Jain & Suchitra S. Acharya. 2020. Hematology in the Adolescent Female. Hematology in the Adolescent Female
51
60
.
F. Zafarghandi Motlagh, M. S. Fallah, H. Bagherian, T. Shirzadeh, S. Ghasri, S. Dabbagh, M. Jamali, Z. Salehi, M. Abiri & S. Zeinali. (2019) Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations. Orphanet Journal of Rare Diseases 14:1.
Crossref
Crossref
H. Yaghootkar, F. Abbasi, N. Ghaemi, A. Rabbani, M. N. Wakeling, P. Eshraghi, S. Enayati, S. Vakili, S. Heidari, K. Patel, F. Sayarifard, S. Borhan‐Dayani, T. J. McDonald, S. Ellard, A. T. Hattersley, M. M. Amoli, R. Vakili & K. Colclough. (2019) Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian population. Diabetic Medicine 36:12, pages 1694-1702.
Crossref
Crossref
Maryam Sobhani, Mohammad Amin Tabatabaiefar, Soudeh Ghafouri-Fard, Asadollah Rajab, Sarah Mozafarpour, Samaneh Nasrniya, Abdol-Mohammad Kajbafzadeh & Mohammad Reza Noori-Daloii. (2019) Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome. Endocrine 66:2, pages 185-191.
Crossref
Crossref
Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Erin Sellars, Sayyed Hossein Nezhadi, Amir Amini, Sanaz Arzhangi, Khadijeh Jalalvand, Peyman Jamali, Zahra Mohammadi, Behzad Davarnia, Pooneh Nikuei, Morteza Oladnabi, Akbar Mohammadzadeh, Elham Zohrehvand, Azim Nejatizadeh, Mohammad Shekari, Maryam Bagherzadeh, Ehsan Shamsi‐Gooshki, Stefan Börno, Bernd Timmermann, Aliakbar Haghdoost, Reza Najafipour, Hamid Reza Khorram Khorshid, Kimia Kahrizi, Reza Malekzadeh, Mohammad R. Akbari & Hossein Najmabadi. (2019) Iranome: A catalog of genomic variations in the Iranian population. Human Mutation 40:11, pages 1968-1984.
Crossref
Crossref
Mahbobeh Koohiyan, Fatemeh Azadegan-Dehkordi, Farideh Koohian & Morteza Hashemzadeh-Chaleshtori. (2019) Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations. Journal of Audiology and Otology 23:4, pages 175-180.
Crossref
Crossref
Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Sirous Zeinali, Andrew Touati, Maryam Abiri, Soheila Sotoudeh, Sara Norouz‐zadeh, Niloufar Amirinezhad, Nikoo Mozafari, Maryam Daneshpazhooh, Hamidreza Mahmoudi, Mohammad Hamid, Jonathan P. Bradfield, Cecilia E. Kim, Hakon Hakonarson & Jouni Uitto. (2018) Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Experimental Dermatology 28:10, pages 1118-1121.
Crossref
Crossref
Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi & Michael Nothnagel. (2019) Distinct genetic variation and heterogeneity of the Iranian population. PLOS Genetics 15:9, pages e1008385.
Crossref
Crossref
Maryam Abiri, Hassan Saei, Maryam Eghbali, Razieh Karamzadeh, Tina Shirzadeh, Zohreh Sharifi & Sirous Zeinali. (2019) Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations. Metabolic Brain Disease 34:4, pages 1145-1156.
Crossref
Crossref
Hao Hu, Kimia Kahrizi, Luciana Musante, Zohreh Fattahi, Ralf Herwig, Masoumeh Hosseini, Cornelia Oppitz, Seyedeh Sedigheh Abedini, Vanessa Suckow, Farzaneh Larti, Maryam Beheshtian, Bettina Lipkowitz, Tara Akhtarkhavari, Sepideh Mehvari, Sabine Otto, Marzieh Mohseni, Sanaz Arzhangi, Payman Jamali, Faezeh Mojahedi, Maryam Taghdiri, Elaheh Papari, Mohammad Javad Soltani Banavandi, Saeide Akbari, Seyed Hassan Tonekaboni, Hossein Dehghani, Mohammad Reza Ebrahimpour, Ingrid Bader, Behzad Davarnia, Monika Cohen, Hossein Khodaei, Beate Albrecht, Sarah Azimi, Birgit Zirn, Milad Bastami, Dagmar Wieczorek, Gholamreza Bahrami, Krystyna Keleman, Leila Nouri Vahid, Andreas Tzschach, Jutta Gärtner, Gabriele Gillessen-Kaesbach, Jamileh Rezazadeh Varaghchi, Bernd Timmermann, Fatemeh Pourfatemi, Aria Jankhah, Wei Chen, Pooneh Nikuei, Vera M. Kalscheuer, Morteza Oladnabi, Thomas F. Wienker, Hans-Hilger Ropers & Hossein Najmabadi. (2018) Genetics of intellectual disability in consanguineous families. Molecular Psychiatry 24:7, pages 1027-1039.
Crossref
Crossref
Ali A. Asadi-Pooya & Zahra Bahrami. (2019) Parental consanguinity in patients with psychogenic nonepileptic seizures. Epilepsy & Behavior 94, pages 167-168.
Crossref
Crossref
Mahbobeh koohiyan, Amirhossein Ahmadi, Farideh koohian, Shahrzad Aghaei, Beheshteh Amiri & Morteza Hashemzadeh-Chaleshtori. (2019) An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review. International Journal of Pediatric Otorhinolaryngology 119, pages 136-140.
Crossref
Crossref
Niloufar Javanrouh, Ali R. Soltanian, Leili Tapak, Fereidoun Azizi, Jurg Ott & Maryam S. Daneshpour. (2018) A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS). Genetic Epidemiology 43:3, pages 342-351.
Crossref
Crossref
Hosien Shahdadi, Mahmood Sheyback, Hosein Rafiemanesh, Abbas Balouchi, Salehoddin Bouya & Gholamhossein Mahmoudirad. (2019) Causes of Chronic Kidney Disease in Iranian Children: A Meta-Analysis and Systematic Review. Annals of Global Health 85:1.
Crossref
Crossref
Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Andrew Touati, Soheila Sotoudeh, Hamidreza Mahmoudi, Parvin Mansouri, Maryam Daneshpazhooh, Nessa Aghazadeh, Kambiz Kamyab Hesari, Mohammadreza Basiri, Eric Londin, Gaurav Kumar, Sirous Zeinali, Paolo Fortina & Jouni Uitto. (2019) Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families. Human Mutation 40:3, pages 288-298.
Crossref
Crossref
Fatemeh Asadi, Seyedeh Moloud Rasouli Ghahfarokhi & Forough Talebi. (2019) Prevalence of Hemoglobin Mutations and Hemoglobinopathies in Masjed Soleiman County, Southeastern Iran. Medical Laboratory Journal 13:2, pages 48-54.
Crossref
Crossref
Babak Behnam & Maryam Zakeri. (2019) Genetics and genomic medicine in Iran. Molecular Genetics & Genomic Medicine 7:2.
Crossref
Crossref
Elham Davoudi-Dehaghani, Nejat Mahdieh, Atefeh Shirkavand, Hamideh Bagherian, Samira DabbaghBagheri & Sirous Zeinali. (2019) SLC26A4 pathogenic variants as a third cause of hearing loss: Role of three exons in DFNB4 deafness in Iran. Indian Journal of Otology 25:3, pages 146.
Crossref
Crossref
Jonathan Spoor, Hamid Farajifard & Nima Rezaei. (2019) Congenital neutropenia and primary immunodeficiency diseases. Critical Reviews in Oncology/Hematology 133, pages 149-162.
Crossref
Crossref
Anu Korula, Anup J. Devasia, N. A. Fouzia, P. N. Nisham, Uday Kulkarni, Kavitha M. Lakshmi, Aby Abraham, Alok Srivastava, Vikram Mathews & Biju George. (2018) Outcomes Following Allogeneic Stem Cell Transplantation Using Non-sibling Family Donors. Indian Journal of Hematology and Blood Transfusion 35:1, pages 43-49.
Crossref
Crossref
Shilpa Jain & Suchitra S. Acharya. (2018) Management of rare coagulation disorders in 2018. Transfusion and Apheresis Science 57:6, pages 705-712.
Crossref
Crossref
Fatemeh Yousefian, Amir Hossein Mahvi, Masud Yunesian, Mohammad Sadegh Hassanvand, Homa Kashani & Heresh Amini. (2018) Long-term exposure to ambient air pollution and autism spectrum disorder in children: A case-control study in Tehran, Iran. Science of The Total Environment 643, pages 1216-1222.
Crossref
Crossref
Mohammad Reza Farzanegan & Hassan F. Gholipour. (2018) Does Gold Price Matter for Divorce Rate in Iran?. Journal of Family and Economic Issues 39:4, pages 588-599.
Crossref
Crossref
Tina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, Shadab Salehpour, Aria Setoodeh, Mohammad Reza Alaei, Leila Youssefian, Ashraf Samavat, Andrew Touati, Mohammad‐Sadegh Fallah, Hassan Vahidnezhad, Morteza Karimipoor, Sarah Azadmehr, Marzieh Raeisi, Ameneh Bandehi Sarhadi, Fatemeh Zafarghandi Motlagh, Mojdeh Jamali, Zahra Zeinali, Maryam Abiri & Sirous Zeinali. (2018) Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Journal of Inherited Metabolic Disease 41:6, pages 1159-1167.
Crossref
Crossref
Marzieh Mojbafan, Ali Khajeh, Haleh Habibi, Hamideh Bagherian & Sirous Zeinali. (2018) Molecular genetic study of Calpainopathy in Iran. Gene 677, pages 259-265.
Crossref
Crossref
Mehdi Shafaat, Mohammad Reza Alaee, Ali Rahmanifar, Aria Setoodeh, Maryam Razzaghy-Azar, Hamideh Bagherian, Samira Dabbagh Bagheri, Fatemeh Zafarghandi Motlagh, Mehrdad Hashemi, Maryam Abiri & Sirous Zeinali. (2018) Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort. Metabolic Brain Disease 33:5, pages 1689-1697.
Crossref
Crossref
Arti Nanda, Lu Liu, Hejab Al‐Ajmi, Qasem A. Al‐Saleh, Suad Al‐Fadhli, John T. Anim, Linda Ozoemena, Jemima E. Mellerio & John A. McGrath. (2018) Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait. International Journal of Dermatology 57:9, pages 1058-1067.
Crossref
Crossref
Mostafa Saadat & Mahdis Zarghami. (2017) CONSANGUINEOUS MARRIAGES AMONG IRANIAN MANDAEANS LIVING IN SOUTH-WEST IRAN. Journal of Biosocial Science 50:4, pages 451-456.
Crossref
Crossref
Mohammad Amin Tabatabaiefar, Mohammad Reza Pourreza, Parisa Tahmasebi, Nader Saki, Morteza Hashemzadeh Chaleshtori, Rasoul Salehi & Javad Mohammadi‐asl. (2018)
A Novel Pathologic Variant in
OTOF
in an Iranian Family Segregating Hereditary Hearing Loss
. Otolaryngology–Head and Neck Surgery 158:6, pages 1084-1092.
Crossref
Crossref
Hamoud Al-Mousa, Ghadah Al-Dakheel, Amal Jabr, Fahd Elbadaoui, Mohamed Abouelhoda, Mansoor Baig, Dorota Monies, Brian Meyer, Abbas Hawwari & Majed Dasouki. (2018) High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots. Frontiers in Immunology 9.
Crossref
Crossref
Hassan Abolhassani, Janet Chou, Wayne Bainter, Craig D. Platt, Mahmood Tavassoli, Tooba Momen, Marzieh Tavakol, Mohammad Hossein Eslamian, Mohammad Gharagozlou, Masoud Movahedi, Mohsen Ghadami, Amir Ali Hamidieh, Gholamreza Azizi, Reza Yazdani, Mohsen Afarideh, Alireza Ghajar, Arash Havaei, Zahra Chavoshzadeh, Seyed Alireza Mahdaviani, Taher Cheraghi, Nasrin Behniafard, Reza Amin, Soheila Aleyasin, Reza Faridhosseini, Farahzad Jabbari-Azad, Mohammamd Nabavi, Mohammad Hassan Bemanian, Saba Arshi, Rasol Molatefi, Roya Sherkat, Mahboubeh Mansouri, Mehrnaz Mesdaghi, Delara Babaie, Iraj Mohammadzadeh, Javad Ghaffari, Alireza Shafiei, Najmeddin Kalantari, Hamid Ahanchian, Maryam Khoshkhui, Habib Soheili, Abbas Dabbaghzadeh, Afshin Shirkani, Rasoul Nasiri Kalmarzi, Seyed Hamidreza Mortazavi, Javad Tafaroji, Abbas Khalili, Javad Mohammadi, Babak Negahdari, Mohammad-Taghi Joghataei, Basel K. al-Ramadi, Capucine Picard, Nima Parvaneh, Nima Rezaei, Talal A. Chatila, Michel J. Massaad, Sevgi Keles, Lennart Hammarström, Raif S. Geha & Asghar Aghamohammadi. (2018) Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency. Journal of Allergy and Clinical Immunology 141:4, pages 1450-1458.
Crossref
Crossref
Mahmoud Reza Ashrafi, Zahra Rezaei, Morteza Heidari, Sedigheh Nikbakht, Reza Azizi Malamiri, Mahmoud Mohammadi, Gholam Reza Zamani, Reza Shervin Badv, Parastoo Rostami, Mojtaba Movahedinia, Mostafa Qorbani, Man Amanat & Ali Reza Tavasoli. (2018) The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System. Journal of Child Neurology 33:4, pages 255-259.
Crossref
Crossref
Monica Zeynalzadeh, Alireza Tafazoli, Azadeh Aarabi, Morteza Moghaddassian, Farah Ashrafzadeh, Massoud Houshmand, Negin Taghehchian & Mohammad Reza Abbaszadegan. (2018)
Four novel mutations of the
BCKDHA
,
BCKDHB
and
DBT
genes in Iranian patients with maple syrup urine disease
. Journal of Pediatric Endocrinology and Metabolism 31:2, pages 205-212.
Crossref
Crossref
Fatemeh Keyfi, Mojila Nasseri, Samira Nayerabadi, Amin Alaei, Armin Mokhtariye & Abdolreza Varasteh. (2018) Frequency of Inborn Errors of Metabolism in a Northeastern Iranian Sample with High Consanguinity Rates. Human Heredity 83:2, pages 71-78.
Crossref
Crossref
Soraya Tremayne. 2018. International Handbook on Gender and Demographic Processes. International Handbook on Gender and Demographic Processes
83
93
.
R. H. Fairoozy, M. Futema, R. Vakili, M. R. Abbaszadegan, S. Hosseini, M. Aminzadeh, H. Zaeri, M. Mobini, S. E. Humphries & A. Sahebkar. (2017) The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population. Scientific Reports 7:1.
Crossref
Crossref
Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Andrew Touati, Soheila Sotoudeh, Maryam Abiri, Mohammadreza Barzegar, Nessa Aghazadeh, Hamidreza Mahmoudi, Sara Norouz-zadeh, Mohammad Hamid, Mahla Zahabiyon, Hamideh Bagherian, Sirous Zeinali, Paolo Fortina & Jouni Uitto. (2017) Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications. Journal of Investigative Dermatology 137:12, pages 2649-2652.
Crossref
Crossref
Nader Ebadi, Abbas Shakoori, Masoumeh Razipour, Arash Salmaninejad, Razieh Zarifian Yeganeh, Saman Mehrabi, Seyed Reza Raeeskarami, Malihea Khaleghian & Hamidreza Azhideh. (2017) The spectrum of Familial Mediterranean Fever gene ( MEFV ) mutations and genotypes in Iran, and report of a novel missense variant (R204H). European Journal of Medical Genetics 60:12, pages 701-705.
Crossref
Crossref
S Riazuddin, M Hussain, A Razzaq, Z Iqbal, M Shahzad, D L Polla, Y Song, E van Beusekom, A A Khan, L Tomas-Roca, M Rashid, M Y Zahoor, W M Wissink-Lindhout, M A R Basra, M Ansar, Z Agha, K van Heeswijk, F Rasheed, M Van de Vorst, J A Veltman, C Gilissen, J Akram, T Kleefstra, M Z Assir, D Grozeva, K Carss, F L Raymond, T D O'Connor, S A Riazuddin, S N Khan, Z M Ahmed, A P M de Brouwer, H van Bokhoven & S Riazuddin. (2016) Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability. Molecular Psychiatry 22:11, pages 1604-1614.
Crossref
Crossref
Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Soheila Sotoudeh, Hamidreza Mahmoudi, Maryam Daneshpazhooh, Nessa Aghazadeh, Rebecca Adams, Alireza Ghanadan, Sirous Zeinali, Paolo Fortina & Jouni Uitto. (2017) Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes. European Journal of Human Genetics 25:11, pages 1282-1285.
Crossref
Crossref
Javad Mohammadi-asl, Mohammad Reza Pourreza, Aliasgar Mohammadi, Ameneh Eskandari, Sima Mozafar-Jalali & Mohammad Amin Tabatabaiefar. (2017) A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred. Journal of Dermatological Science 88:1, pages 134-138.
Crossref
Crossref
Mohammad Amin Tabatabaiefar, Paria Alipour, Azam Pourahmadiyan, Najmeh Fattahi, Laleh Shariati, Neda Golchin & Javad Mohammadi-Asl. (2017) A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. Journal of the Neurological Sciences 379, pages 212-216.
Crossref
Crossref
Hamoud Al-Mousa & Bandar Al-Saud. (2017) Primary Immunodeficiency Diseases in Highly Consanguineous Populations from Middle East and North Africa: Epidemiology, Diagnosis, and Care. Frontiers in Immunology 8.
Crossref
Crossref
Tohid Ghasemnejad, Mahmoud Shekari Khaniani, Fatemeh Zarei, Mina Farbodnia & Sima Mansoori Derakhshan. (2017) An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population. International Journal of Pediatric Otorhinolaryngology 97, pages 113-126.
Crossref
Crossref
Reza Fadaye-Vatan, Ahmad Delbari, Elham Lotfalinezhad, Fatemeh Amini, Kurosh Gharagozli, Jafar Bolhari, Parviz Bahrami, Vida Saii, Amir Ahmadi, Zahra Moghadam, Abdulaziz Aflakseir & Devender Bhalla. (2018) Measurement and associative factors of adherence to epilepsy drug treatment among the elderly population in Tehran (Iran). International Journal of Epilepsy 04:01, pages 046-050.
Crossref
Crossref
Hasti Hadizadeh, Masoud Salehi, Shabnam Khoramnejad, Kia Vosoughi & Nima Rezaei. (2017) The association between parental consanguinity and primary immunodeficiency diseases: A systematic review and meta‐analysis. Pediatric Allergy and Immunology 28:3, pages 280-287.
Crossref
Crossref
Jalal Heshmatnia, Majid Marjani, Seyed Alireza Mahdaviani, Parvaneh Adimi, Mihan Pourabdollah, Payam Tabarsi, Fereshte Mahdavi, Hamidreza Jamaati, Ian M. Adcock, Johan Garssen, Aliakbar Velayati, Davood Mansouri & Esmaeil Mortaz. (2017) Paecilomyces formosus Infection in an Adult Patient with Undiagnosed Chronic Granulomatous Disease. Journal of Clinical Immunology 37:4, pages 342-346.
Crossref
Crossref
Faravareh Khordadpoor Deilamani & Mohammad Taghi Akbari. (2017) Potential Founder Effect of Tyrosinase Gene Mutations in Oculocutaneous Albinism Families from West of Iran. Journal of Human Genetics and Genomics 1:1.
Crossref
Crossref
Ahmed KhattabShozeb Haider, Ameet KumarSamarth DhawanDauood AlamRaquel RomeroJames BurnsDi LiJessica EstaticoSimran RahiSaleel FatimaAli AlzahraniMona HafezNoha MusaMaryam Razzghy AzarNajoua KhaloulMoez GribaaAli SaadIlhem Ben CharfeddineBerenice Bilharinho de MendonçaAlicia BelgoroskyKatja DumicMiroslav DumicJavier AisenbergNurgun KandemirAyfer AlikasifogluAlev OzonNazli GoncTina ChengUrsula Kuhnle-KrahlMarco CappaPaul-Martin HolterhusMunier A. NourDaniele Pacaud, Assaf HoltzmanSun LiMone ZaidiTony YuenMaria I. New. (2017) Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Proceedings of the National Academy of Sciences 114:10.
Crossref
Crossref
Hassan Vahidnezhad, Leila Youssefian, Sirous Zeinali, Amir Hossein Saeidian, Soheila Sotoudeh, Nikoo Mozafari, Maryam Abiri, Abdol-Mohammad Kajbafzadeh, Mohammadreza Barzegar, Adam Ertel, Paolo Fortina & Jouni Uitto. (2017) Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages. Journal of Investigative Dermatology 137:3, pages 660-669.
Crossref
Crossref
Maryam Abiri, Razieh Karamzadeh, Marziyeh Mojbafan, Mohammad Reza Alaei, Atefeh Jodaki, Masomeh Safi, Soodeh Kianfar, Ameneh Bandehi Sarhaddi, Mohammad Reza Noori-Daloii, Morteza Karimipoor & Sirous Zeinali. (2016) In silico analysis of novel mutations in maple syrup urine disease patients from Iran. Metabolic Brain Disease 32:1, pages 105-113.
Crossref
Crossref
A Nariman, MR Sobhan, M Savaei, E Aref-Eshghi, R Nourinejad, M Manoochehri, S Ghahremani, F Daliri & K Daliri. (2016) The genetic background of Southern Iranian couples before marriage. Balkan Journal of Medical Genetics 19:2, pages 71-74.
Crossref
Crossref
Saba Sheikhbahaei, Roya Sherkat, Dirk Roos, Majid Yaran, Somayeh Najafi & Alireza Emami. (2016) Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in Iran. Allergy, Asthma & Clinical Immunology 12:1.
Crossref
Crossref
Mohammad Atari & Ramin Jamali. (2016) Mate Preferences in Young Iranian Women: Cultural and Individual Difference Correlates. Evolutionary Psychological Science 2:4, pages 247-253.
Crossref
Crossref
Fatemeh Godrati, Narjes Saadatmand, Maryam Dinpazhoh & Marzieh Akbarzadeh. (2016) Epidemiological Study of Legal Abortion due to Fetal Defects in the Files Referred to Fars Province Forensic Medicine Centers from 2007 to 2013. Shiraz E-Medical Journal 17:11.
Crossref
Crossref
Helia Maghzi, Vahid Shaygannejad, Alireza Minagar, Akbar Hassanzadeh & Amir-Hadi Maghzi. (2016) Consanguinity and multiple sclerosis susceptibility: A case control study. Multiple Sclerosis and Related Disorders 10, pages 179-180.
Crossref
Crossref
Mohammad Ajallouyan, Shokofeh Radfar, Sima Nouhi, Seid Abbas Tavallaie, Susan Amirsalari, Jaleh Yousefi & Mahdieh Hasanali Fard. (2016) Consanguinity Among Parents of Iranian Deaf Children. Iranian Red Crescent Medical Journal 18:11.
Crossref
Crossref
Shiva Saghafi, Zahra Pourpak, Franziska Nussbaumer, Mohammad Reza Fazlollahi, Massoud Houshmand, Amir Ali Hamidieh, Mohammad Hassan Bemanian, Mohammad Nabavi, Nima Parvaneh, Bodo Grimbacher, Mostafa Moin & Cristina Glocker. (2016)
DOCK
8
deficiency in six Iranian patients
. Clinical Case Reports 4:6, pages 593-600.
Crossref
Crossref
Faravareh Khordadpoor-Deilamani, Mohammad Taghi Akbari, Morteza Karimipoor & Gholam Reza Javadi. (2016) Homozygosity mapping in albinism patients using a novel panel of 13 STR markers inside the nonsyndromic OCA genes: introducing 5 novel mutations. Journal of Human Genetics 61:5, pages 373-379.
Crossref
Crossref
Fatemeh Yazdani, Ashraf Kazemi, Marjaneh M. Fooladi & Hamid R. Oreyzi Samani. (2016) The relations between marital quality, social support, social acceptance and coping strategies among the infertile Iranian couples. European Journal of Obstetrics & Gynecology and Reproductive Biology 200, pages 58-62.
Crossref
Crossref
Maryam Abiri, Razieh Karamzadeh, Morteza Karimipoor, Shirin Ghadami, Mohammad Reza Alaei, Samira Dabagh Bagheri, Hamideh Bagherian, Aria Setoodeh, Mohammad Reza Noori-Daloii & Sirous Zeinali. (2016) Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 786, pages 34-40.
Crossref
Crossref
Yi Feng, Yuan‐Yuan Wu, Xiao‐Juan Lin, Lu Yang, Zhi‐Juan Luo, Ying‐Hui Zhou, Jing Chen, Ning Li, Zhong Lin & Xia Zhao. (2015) Associations between the codon 72 polymorphism of the TP53 gene and the risk of recurrent implantation failure. Journal of Obstetrics and Gynaecology Research 42:2, pages 184-189.
Crossref
Crossref
Nazanin Boujarian, Mohd Tajudin Ninggal, Ssekamanya Siraje Abdallah & Masoud Noroozi. (2016) Domestic Violence Subjected to Different Patterns of Cultural Marriage. Open Journal of Social Sciences 04:05, pages 87-98.
Crossref
Crossref
Maryam Abiri, Saeed Talebi, Jouni Uitto, Leila Youssefian, Hassan Vahidnezhad, Tina Shirzad, Shadab Salehpour & Sirous Zeinali. (2016) Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinity. Journal of Pediatric Endocrinology and Metabolism 29:10.
Crossref
Crossref
Senthil Senniappan, Atefeh Sadeghizadeh, Sarah E Flanagan, Sian Ellard, Mahin Hashemipour, Majid Hosseinzadeh, Mansour Salehi & Khalid Hussain. (2015) Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia. BMC Research Notes 8:1.
Crossref
Crossref
Christina M Sloan-Heggen, Mojgan Babanejad, Maryam Beheshtian, Allen C Simpson, Kevin T Booth, Fariba Ardalani, Kathy L Frees, Marzieh Mohseni, Reza Mozafari, Zohreh Mehrjoo, Leila Jamali, Saeideh Vaziri, Tara Akhtarkhavari, Niloofar Bazazzadegan, Nooshin Nikzat, Sanaz Arzhangi, Farahnaz Sabbagh, Hasan Otukesh, Seyed Morteza Seifati, Hossein Khodaei, Maryam Taghdiri, Nicole C Meyer, Ahmad Daneshi, Mohammad Farhadi, Kimia Kahrizi, Richard JH Smith, Hela Azaiez & Hossein Najmabadi. (2015) Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. Journal of Medical Genetics 52:12, pages 823-829.
Crossref
Crossref
Azim Mehrvar, Maryam Tashvighi, Mohammad Faranoush, Dirk Reinhardt, Naghmeh Niktoreh Mofrad, Amir Abbas Hedayati Asl & Mardawij Alebouyeh. (2015) Family History and Relapse in Pediatric Acute Myeloid Leukemia. Pediatric Blood & Cancer 62:12, pages 2235-2237.
Crossref
Crossref
Ariela Gordon‐Shaag, Michel Millodot, Igor Kaiserman, Tzahi Sela, Guy Barnett Itzhaki, Yaffa Zerbib, Efrat Matityahu, Shira Shkedi, Svetlana Miroshnichenko & Einat Shneor. (2015) Risk factors for keratoconus in Israel: a case–control study. Ophthalmic and Physiological Optics 35:6, pages 673-681.
Crossref
Crossref
Siavash Maghsoudlou, Sven Cnattingius, Mohsen Aarabi, Scott M. Montgomery, Shahriar Semnani, Olof Stephansson, Anna‐Karin Wikström & Shahram Bahmanyar. (2015) Consanguineous marriage, prepregnancy maternal characteristics and stillbirth risk: a population‐based case–control study. Acta Obstetricia et Gynecologica Scandinavica 94:10, pages 1095-1101.
Crossref
Crossref
Seyed Mohammad Seyedhassani, Feyzollah Hashemi-Gorji, Mahdieh Yavari & Reza Mirfakhraie. (2015) Novel missense mutation in the GALNS gene in an affected patient with severe form of mucopolysaccharidosis type IVA. Clinica Chimica Acta 450, pages 121-124.
Crossref
Crossref
Seyed Behzad Jazayeri, Soheil Saadat, Rashid Ramezani & Ahmad Kaviani. (2015) Incidence of primary breast cancer in Iran: Ten-year national cancer registry data report. Cancer Epidemiology 39:4, pages 519-527.
Crossref
Crossref
Mehdi Mirzaei Alavijeh, Firoozeh Mostafavi, Mohammad Ahmadpanah, Behzad Karami Matin, Mohamad Reza Amoei & Farzad Jalilian. (2015) Murder and Motivation: A Qualitative Study. Avicenna Journal of Neuro Psych Physiology 2:2.
Crossref
Crossref
Mehdi Mirzaei Alavijeh, Firoozeh Mostafavi, Mohammad Ahmadpanah, Behzad Karami Matin, Mohamad Reza Amoei & Farzad Jalilian. (2015) Murder and Motivation: A Qualitative Study. Avicenna Journal of Neuro Psych Physiology 2:2.
Crossref
Crossref
Parisa Tahmasebi & Seyed Reza Kazemi Nezhad. (2015) An Overview of Hereditary Diseases in Khuzestan Province, Southwest Iran. Gene, Cell and Tissue 2:2.
Crossref
Crossref
Mansooreh Bagheri, Majid Farvardin & Mostafa Saadat. (2015) A study of consanguineous marriage as a risk factor for developing comitant strabismus. Journal of Community Genetics 6:2, pages 177-180.
Crossref
Crossref
Roberta Palla, Flora PeyvandiAmy D. Shapiro. (2015) Rare bleeding disorders: diagnosis and treatment. Blood 125:13, pages 2052-2061.
Crossref
Crossref
Kimia Kahrizi & Hossein Najmabadi. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences
1
21
.
Mohammad R. Deemeh, Marziyeh Tavalaee & Mohammad H. Nasr-Esfahani. (2015) Health of Children Born Through Artificial Oocyte Activation. Reproductive Sciences 22:3, pages 322-328.
Crossref
Crossref
Rajech Sharkia, Muhammad Mahajnah, Muhammad Athamna, Ahmad Sheikh-Muhammad & Abdelnaser Zalan. (2015) Variations in Types of First-Cousin Marriages over a Two-Generation Period among Arabs in Israel. Advances in Anthropology 05:04, pages 171-176.
Crossref
Crossref
F. Khamoushi, S. Ahmadi, B. Karami-Matin, T. Ahmadi-Jouybari, M. Mirzaei-Alavijeh, M. Mahboubi & M. Ataee. (2015) Prevalence and Socio-Demographic Characteristics Related to Stress, Anxiety, and Depression among Patients with Major Tha-lassemia in the Kermanshah County. Journal of Biology and Today's World 4:3.
Crossref
Crossref
Ariela Gordon-Shaag, Michel Millodot, Einat Shneor & Yutao Liu. (2015) The Genetic and Environmental Factors for Keratoconus. BioMed Research International 2015, pages 1-19.
Crossref
Crossref
Mostafa Saadat. (2015) Association between consanguinity and survival of marriages. Egyptian Journal of Medical Human Genetics 16:1, pages 67-70.
Crossref
Crossref
F Zeinali, M Mohseni, M Fadaee, Z Fattahi, H Najmabadi, H Otukesh & K Kahrizi. (2014)
Investigation of
ATP6V1B1
and
ATP6V0A4
genes causing hereditary hearing loss associated with distal renal tubular acidosis in Iranian families
. The Journal of Laryngology & Otology 128:12, pages 1056-1059.
Crossref
Crossref
Camila Wenceslau Alvarez, Maria Leine Guion-Almeida & Antonio Richieri-Costa. (2014) Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement. Journal of Cranio-Maxillofacial Surgery 42:8, pages 1952-1957.
Crossref
Crossref
Hamed Momeni-Moghaddam, Jason S. Ng, Hassan Robabi & Farshid Yaghubi. (2014) Color Vision Deficiency in Zahedan, Iran. Optometry and Vision Science 91:11, pages 1372-1376.
Crossref
Crossref
Mari Ataee, Kambiz Karimzadeh-Shirazi, Touraj Ahmadi-Jouybari, Behzad Kara-miMatin, Abbas Aghaei & Fazel Zinat-Motlagh. (2014) Cognitive Predictors of Cousin Marriage Among Couples Visiting Counseling Centers in Kohgiluyeh-Boyer Ahmad Province. Journal of Education and Community Health 1:3, pages 47-53.
Crossref
Crossref
Heba J. SabbaghMona Hassan Ahmed HassanNicola P. T. InnesAlaa Al BaikPeter A. Mossey. (2014) Parental Consanguinity and Nonsyndromic Orofacial Clefts in Children: A Systematic Review and Meta-Analyses. The Cleft Palate-Craniofacial Journal 51:5, pages 501-513.
Crossref
Crossref
Hassan Hashemi, Mehdi Khabazkhoob, Negareh Yazdani, Hadi Ostadimoghaddam, Reza Norouzirad, Kazem Amanzadeh, Mohammad Miraftab, Akbar Derakhshan & AbbasAli Yekta. (2014) The prevalence of keratoconus in a young population in Mashhad, Iran. Ophthalmic and Physiological Optics 34:5, pages 519-527.
Crossref
Crossref
AFTAB ALAM STHANADAR, ALAN H. BITTLES & MUHAMMAD ZAHID. (2013) CIVIL UNREST AND THE CURRENT PROFILE OF CONSANGUINEOUS MARRIAGE IN KHYBER PAKHTUNKHWA PROVINCE, PAKISTAN. Journal of Biosocial Science 46:5, pages 698-701.
Crossref
Crossref
Ramez Barbara, Ariela Gordon-Shaag, Michel Millodot, Einat Shneor, Maron Essa & Miriam Anton. (2014) Prevalence of Keratoconus among Young Arab students in Israel. International Journal of Keratoconus and Ectatic Corneal Diseases 3:1, pages 9-14.
Crossref
Crossref
Pegah Bronoosh, Maryam Kasraeian & Bita Ghazi Saeedi. (2014) Oral abnormalities in an Iranian newborn population. Pediatric Dental Journal 24:1, pages 8-11.
Crossref
Crossref
Hasan Mottaghi Moghaddam Shahri, Reza Jafarzadeh Esfehani, Nader Yazdan Panah & Ali Jafarzadeh Esfehani. (2014) Consanguinity and isolated atrial septal defect in North East of Iran. Annals of Saudi Medicine 34:2, pages 147-152.
Crossref
Crossref
MOSTAFA SAADAT & KHADIJEH TAJBAKHSH. (2012) PREVALENCE OF CONSANGUINEOUS MARRIAGES IN WEST AND SOUTH OF AFGHANISTAN. Journal of Biosocial Science 45:6, pages 799-805.
Crossref
Crossref
Maryam Sobhani, Mohammad Amin Tabatabaiefar, Asadollah Rajab, Abdol-Mohammad Kajbafzadeh & Mohammad Reza Noori-Daloii. (2013) Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms. Gene 528:2, pages 309-313.
Crossref
Crossref
GHADIR EL-KHESHEN & MOSTAFA SAADAT. (2013) PREVALENCE OF CONSANGUINEOUS MARRIAGES AMONG SHI'A POPULATIONS OF LEBANON. Journal of Biosocial Science 45:5, pages 675-682.
Crossref
Crossref
Elham Davoudi-Dehaghani, Sirous Zeinali, Nejat Mahdieh, Atefeh Shirkavand, Hamideh Bagherian & Mohammad Amin Tabatabaiefar. (2013) A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect. International Journal of Pediatric Otorhinolaryngology 77:5, pages 821-826.
Crossref
Crossref
Nizar Ben Halim, Nissaf Ben Alaya Bouafif, Lilia Romdhane, Rym Kefi Ben Atig, Ibtissem Chouchane, Yosra Bouyacoub, Imen Arfa, Wafa Cherif, Sonia Nouira, Faten Talmoudi, Khaled Lasram, Sana Hsouna, Welid Ghazouani, Hela Azaiez, Leila El Matri, Abdelmajid Abid, Neji Tebib, Marie-Françoise Ben Dridi, Salem Kachboura, Ahlem Amouri, Mourad Mokni, Saida Ben Arab, Koussay Dellagi & Sonia Abdelhak. (2012) Consanguinity, endogamy, and genetic disorders in Tunisia. Journal of Community Genetics 4:2, pages 273-284.
Crossref
Crossref
Angela Posch, Stephanie Springer, Martin Langer, Wibke Blaicher, Berthold Streubel & Maximilian Schmid. (2012) Prenatal genetic counseling and consanguinity. Prenatal Diagnosis 32:12, pages 1133-1138.
Crossref
Crossref
Mojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, Carla Nishimura, Nicole Meyer, Nooshin Nikzat, Elahe Sohrabi, Amin Najmabadi, Peyman Jamali, Farkhonde Habibi, Richard J.H. Smith, Kimia Kahrizi & Hossein Najmabadi. (2012) A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. American Journal of Medical Genetics Part A 158A:10, pages 2485-2492.
Crossref
Crossref
Mostafa Saadat. (2012) Influence of parental consanguineous marriages on age at onset of bipolar disorder. Psychiatry Research 198:2, pages 327-328.
Crossref
Crossref
Bahareh RabbaniNejat MahdiehMohammad Tahgi Haghi AshtianiBagher LarijaniMohammad Taghi AkbariMaria NewAlan ParsaJan P. SchoutenAli Rabbani. (2012)
Mutation Analysis of the
CYP21A2
Gene in the Iranian Population
. Genetic Testing and Molecular Biomarkers 16:2, pages 82-90.
Crossref
Crossref
Behzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, Nooshin Nikzat, Niloofar Bazazzadegan, Akbar Pirzade, Reza Farajollahi, Carla Nishimura, Khadijeh Jalalvand, Sanaz Arzhangi, Kimia Kahrizi, Richard J.H. Smith & Hossein Najmabadi. (2012) Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss. International Journal of Pediatric Otorhinolaryngology 76:2, pages 268-271.
Crossref
Crossref
KHYBER SAIFY & MOSTAFA SAADAT. (2011) CONSANGUINEOUS MARRIAGES IN AFGHANISTAN. Journal of Biosocial Science 44:1, pages 73-81.
Crossref
Crossref
Nima Rezaei, Payam Mohammadinejad & Asghar Aghamohammadi. (2011) The demographics of primary immunodeficiency diseases across the unique ethnic groups in Iran, and approaches to diagnosis and treatment. Annals of the New York Academy of Sciences 1238:1, pages 24-32.
Crossref
Crossref
Fatemeh Fattahi, Mohsen Badalzadeh, Leyla Sedighipour, Masoud Movahedi, Mohammad Reza Fazlollahi, Seyed Davood Mansouri, Ghamar Taj Khotaei, Mohammad Hassan Bemanian, Fatemeh Behmanesh, Amir Ali Hamidieh, Nasrin Bazargan, Setareh Mamishi, Fariborz Zandieh, Zahra Chavoshzadeh, Iraj Mohammadzadeh, Seyed Alireza Mahdaviani, Seyed Ahmad Tabatabaei, Najmeddin Kalantari, Shaghayegh Tajik, Marzieh Maddah, Zahra Pourpak & Mostafa Moin. (2011) Inheritance Pattern and Clinical Aspects of 93 Iranian Patients with Chronic Granulomatous Disease. Journal of Clinical Immunology 31:5, pages 792-801.
Crossref
Crossref
Nejat MahdiehBahareh RabbaniAtefeh ShirkavandHamideh BagherianZahra Shahab MovahedPaanti FouladiFaezeh RahiminejadMasoumeh MasoudifardMohammad Taghi AkbariSirous Zeinali. (2011)
Impact of Consanguineous Marriages in
GJB2
-Related Hearing Loss in the Iranian Population: A Report of a Novel Variant
. Genetic Testing and Molecular Biomarkers 15:7-8, pages 489-493.
Crossref
Crossref
MOSTAFA SAADAT. (2011) ASSOCIATION BETWEEN HEALTHY LIFE EXPECTANCY AT BIRTH AND CONSANGUINEOUS MARRIAGES IN 63 COUNTRIES. Journal of Biosocial Science 43:4, pages 475-480.
Crossref
Crossref
Lin-Lin Wang, Ying-Ying Jin, Yi-Qun Hao, Juan-Juan Wang, Chun-Mei Yao, Xi Wang, Rui-Ming Cao, Hui Zhang, Yi Chen & Tong-Xin Chen. (2011) Distribution and Clinical Features of Primary Immunodeficiency Diseases in Chinese Children (2004–2009). Journal of Clinical Immunology 31:3, pages 297-308.
Crossref
Crossref
Yasemin I. Balcı, Betul Tavil, Cagman S. Tan, Tuba T. Ozgur, Burcu Bulum, Mualla Cetin, Mustafa Balcı, Songul Yalcın, Ilhan Tezcan & Duygu Uckan. (2011) Increased availability of family donors for hematopoietic stem cell transplantation in a population with increased incidence of consanguinity. Clinical Transplantation 25:3, pages 475-480.
Crossref
Crossref
Stéphanie Boisson-Dupuis, Jamila El Baghdadi, Nima Parvaneh, Aziz Bousfiha, Jacinta Bustamante, Jacqueline Feinberg, Arina Samarina, Audrey V. Grant, Lucile Janniere, Naima El Hafidi, Amal Hassani, Daniel Nolan, Jilali Najib, Yildiz Camcioglu, Nevin Hatipoglu, Cigdem Aydogmus, Gonul Tanir, Caner Aytekin, Melike Keser, Ayper Somer, Guside Aksu, Necil Kutukculer, Davood Mansouri, Alireza Mahdaviani, Setareh Mamishi, Alexandre Alcais, Laurent Abel & Jean-Laurent Casanova. (2011) IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey. PLoS ONE 6:4, pages e18524.
Crossref
Crossref
Samane Nafissi, Maryam Ansari-Lari & Mostafa Saadat. (2011) Parental consanguineous marriages and age at onset of schizophrenia. Schizophrenia Research 126:1-3, pages 298-299.
Crossref
Crossref
Zahra Anvar, Bahia Namavar-Jahromi & Mostafa Saadat. (2010) Association between consanguineous marriages and risk of pre-eclampsia. Archives of Gynecology and Obstetrics 283:S1, pages 5-7.
Crossref
Crossref
LALEH RAFIEE & MOSTAFA SAADAT. (2010) PREVALENCE OF CONSANGUINEOUS MARRIAGES AMONG IRANIAN GEORGIANS. Journal of Biosocial Science 43:1, pages 47-50.
Crossref
Crossref
Munira Borhany, Zaen Pahore, Zeeshan ul Qadr, Muhammad Rehan, Arshi Naz, Asif Khan, Saqib Ansari, Tasneem Farzana, Muhammad Nadeem, Syed Amir Raza & Tahir Shamsi. (2010) Bleeding disorders in the tribe: result of consanguineous in breeding. Orphanet Journal of Rare Diseases 5:1.
Crossref
Crossref
Mostafa Saadat & Roghayyeh Vakili-Ghartavol. (2010) Parental consanguinity and susceptibility to drug abuse among offspring, a case–control study. Psychiatry Research 180:1, pages 57-59.
Crossref
Crossref
Mostafa Saadat & Iraj Saadat. (2010) Correlation between consanguineous marriages and age-standardized mortality rate due to breast cancer, an ecologic study. Breast Cancer Research and Treatment 121:3, pages 795-797.
Crossref
Crossref
SAMANE NAFISSI, MARYAM ANSARI-LARI & MOSTAFA SAADAT. (2009) EFFECT OF INBREEDING ON WEIGHT GAIN OF OFFSPRING FROM BIRTH TO 12 MONTHS AFTER BIRTH: A STUDY FROM IRAN. Journal of Biosocial Science 42:2, pages 195-200.
Crossref
Crossref
Alan H. Bittles. 2010. Vogel and Motulsky's Human Genetics. Vogel and Motulsky's Human Genetics
507
528
.
Mohammad Jalal Abbasi‐Shavazi, S. Philip Morgan, Meimanat Hossein‐Chavoshi & Peter McDonald. (2009) Family Change and Continuity in Iran: Birth Control Use Before First Pregnancy. Journal of Marriage and Family 71:5, pages 1309-1324.
Crossref
Crossref
N. M. Ghiasvand, A. Aledavood, R. Ghiasvand, F. Seyedin Borojeny, A. R. Aledavood, S. Seyed, W. Miner & G. R. Saeb Taheri. (2009) Prevalence of classical phenylketonuria in mentally retarded individuals in Iran. Journal of Inherited Metabolic Disease 32:S1, pages 283-287.
Crossref
Crossref
HASAN OTHMAN & MOSTAFA SAADAT. (2009) PREVALENCE OF CONSANGUINEOUS MARRIAGES IN SYRIA. Journal of Biosocial Science 41:5, pages 685-692.
Crossref
Crossref
Ali Reza Pouya, Seyedeh Sedigheh Abedini, Neda Mansoorian, Farkhondeh Behjati, Nooshin Nikzat, Marzieh Mohseni, Sahar Esmaeeli Nieh, Lia Abbasi Moheb, Hossein Darvish, Gholamreza Bahrami Monajemi, Susan Banihashemi, Kimia Kahrizi, Hans Hilger Ropers & Hossein Najmabadi. (2009) Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population. European Journal of Medical Genetics 52:4, pages 170-173.
Crossref
Crossref
Marcia C. Inhorn, Loulou Kobeissi, Zaher Nassar, Da'ad Lakkis & Michael H. Fakih. (2009) Consanguinity and family clustering of male factor infertility in Lebanon. Fertility and Sterility 91:4, pages 1104-1109.
Crossref
Crossref
Seyed Mohammad Akrami, Vahideh Montazeri, Somaieh Rashid Shomali, Ramin Heshmat & Bagher Larijani. (2008) Is There a Significant Trend in Prevalence of Consanguineous Marriage in Tehran? A Review of Three Generations. Journal of Genetic Counseling 18:1, pages 82-86.
Crossref
Crossref
Mohammad Jalal Abbasi-Shavazi, Peter McDonald & Meimanat Hosseini-Chavoshi. 2009. The Fertility Transition in Iran: Revolution and Reproduction. The Fertility Transition in Iran: Revolution and Reproduction
135
161
.
Zahra Zendeh-Boodi & Mostafa Saadat. (2007) Genetic polymorphism of GSTT1 may be under natural selection in a population chronically exposed to natural sour gas. Molecular Biology Reports 35:4, pages 673-676.
Crossref
Crossref
Mohsen Fathzadeh, Mohammad Ali Babaie Bigi, Masood Bazrgar, Majid Yavarian, Hamid Reza Tabatabaee & Seyed Mohammad Akrami. (2008) Genetic Counseling in Southern Iran: Consanguinity and Reason for Referral. Journal of Genetic Counseling 17:5, pages 472-479.
Crossref
Crossref
Mohsen Esmaeili, Mortaza Bonyadi, Mandana Rafeey, Kazem Sakha & Mohammad Hossein Somi. (2008) Common MEFV Mutation Analysis in Iranian Azeri Turkish Patients with Familial Mediterranean Fever. Seminars in Arthritis and Rheumatism 37:5, pages 334-338.
Crossref
Crossref
Suzanne E. Joseph. (2007) “Kissing Cousins”. Current Anthropology 48:5, pages 756-764.
Crossref
Crossref
Mahnaz Sadeghi Shabestari, Seyyed Hadi Maljaei, Reza Baradaran, Mohammad Barzegar, Fazileh Hashemi, Adel Mesri & Nima Rezaei. (2007) Distribution of Primary Immunodeficiency Diseases in the Turk Ethnic Group, Living in the Northwestern Iran. Journal of Clinical Immunology 27:5, pages 510-516.
Crossref
Crossref
Mostafa Moin, Asghar Aghamohammadi, Ali Kouhi, Sanaz Tavassoli, Nima Rezaei, Saeed-Reza Ghaffari, Mohammad Gharagozlou, Masoud Movahedi, Zahra Purpak, Bahram MirSaeid Ghazi, Maryam Mahmoudi & Abolhasan Farhoudi. (2007) Ataxia-Telangiectasia in Iran: Clinical and Laboratory Features of 104 Patients. Pediatric Neurology 37:1, pages 21-28.
Crossref
Crossref
Abdulbari Bener & Rafat Hussain. (2006) Consanguineous unions and child health in the State of Qatar. Paediatric and Perinatal Epidemiology 20:5, pages 372-378.
Crossref
Crossref
Mostafa Saadat & Zahra Zendeh-Boodi. (2006) Correlation Between Incidences of Self-inflicted Burns and Means of Inbreeding Coefficients, an Ecologic Study. Annals of Epidemiology 16:9, pages 708-711.
Crossref
Crossref
Nima Rezaei, Zahra Pourpak, Asghar Aghamohammadi, Abolhassan Farhoudi, Masoud Movahedi, Mohammad Gharagozlou, Bahram MirSaeid Ghazi, Lida Atarod, Kamran Abolmaali, Maryam Mahmoudi, Davoud Mansouri, Saba Arshi, Naser Javaher Tarash, Roya Sherkat, Reza Amin, Sara Kashef, Reza Farid Hosseini, Iraj Mohammadzadeh, Mehrnaz Sadeghi Shabestari, Mohammad Nabavi & Mostafa Moin. (2006) Consanguinity in Primary Immunodeficiency Disorders; the Report from Iranian Primary Immunodeficiency Registry. American Journal of Reproductive Immunology 56:2, pages 145-151.
Crossref
Crossref
Mahnoush Babaei, Midori Mitui, Eric R. Olson & Richard A. Gatti. (2005) ATM haplotypes and associated mutations in Iranian patients with ataxia–telangiectasia: recurring homozygosity without a founder haplotype. Human Genetics 117:2-3, pages 101-106.
Crossref
Crossref
Mostafa Saadat. (2005) Epidemiology and mortality of hospitalized burn patients in Kohkiluye va Boyerahmad province (Iran): 2002–2004. Burns 31:3, pages 306-309.
Crossref
Crossref