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Shilpa D. Kadam. (2023) Open Sesame: Door to Enriched Somatic Variants Underlying Sporadic mTLE. Epilepsy Currents 23:6, pages 383-385.
Crossref
Crossref
Sarah E. Sheppard, Michael E. March, Christoph Seiler, Leticia S. Matsuoka, Sophia E. Kim, Charlly Kao, Adam I. Rubin, Mark R. Battig, Nahla Khalek, Erica Schindewolf, Nora O’Connor, Erin Pinto, Jessica R.C. Priestley, Victoria R. Sanders, Rojeen Niazi, Arupa Ganguly, Cuiping Hou, Diana Slater, Ilona J. Frieden, Thy Huynh, Joseph T. Shieh, Ian D. Krantz, Jessenia C. Guerrero, Lea F. Surrey, David M. Biko, Pablo Laje, Leslie Castelo-Soccio, Taizo A. Nakano, Kristen Snyder, Christopher L. Smith, Dong Li, Yoav Dori & Hakon Hakonarson. (2023) Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition. JCI Insight 8:9.
Crossref
Crossref
Sahibjot Sran & Tracy A. Bedrosian. (2023) RAS pathway: The new frontier of brain mosaicism in epilepsy. Neurobiology of Disease 180, pages 106074.
Crossref
Crossref
Vianey Ordoñez-Labastida, Tania Barragán Arévalo & Oscar F. Chacon-Camacho. 2020. Genetic Syndromes. Genetic Syndromes
1
4
.
Nya D. Nelson, Feng Xu, Prashant Chandrasekaran, Leslie A. Litzky, William H. Peranteau, David B. Frank, Marilyn Li & Jennifer Pogoriler. (2022) Defining the spatial landscape of KRAS mutated congenital pulmonary airway malformations: a distinct entity with a spectrum of histopathologic features. Modern Pathology 35:12, pages 1870-1881.
Crossref
Crossref
Victorya Zakharova, Elena Raykina, Irina Mersiyanova, Ekaterina Deordieva, Dmitry Pershin, Victorya Vedmedskia, Yulia Rodina, Natalia Kuzmenko, Michael Maschan & Anna Shcherbina. (2022)
Cancer‐causing
MAP2K1
mutation in a mosaic patient with cardio‐facio‐cutaneous syndrome and immunodeficiency
. Human Mutation 43:12, pages 1852-1855.
Crossref
Crossref
Diana Carli, Nicoletta Resta, Giovanni Battista Ferrero, Martino Ruggieri & Alessandro Mussa. (2022) Mosaic RASopathies: A review of disorders caused by somatic pathogenic variants in the genes of the RAS/MAPK pathway. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 190:4, pages 520-529.
Crossref
Crossref
Martin Zenker. (2022)
Clinical overview on
RASopathies
. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 190:4, pages 414-424.
Crossref
Crossref
Alessandro Mussa, Antonella Turchiano, Simona Cardaropoli, Paola Coppo, Antonino Pantaleo, Rosanna Bagnulo, Carlotta Ranieri, Matteo Iacoviello, Antonella Garganese, Alessandro Stella, Stefano Gabriele Vallero, Daniele Bertin, Federica Santoro, Diana Carli, Giovanni Battista Ferrero & Nicoletta Resta. (2022)
Lateralized overgrowth with vascular malformation caused by a somatic
PTPN11
pathogenic variant: Another piece added to the puzzle of mosaic
RASopathies
. Genes, Chromosomes and Cancer 61:11, pages 689-695.
Crossref
Crossref
Josh N. Vo, Yi-Mi Wu, Jeanmarie Mishler, Sarah Hall, Rahul Mannan, Lisha Wang, Yu Ning, Jin Zhou, Alexander C. Hopkins, James C. Estill, Wallace K. B. Chan, Jennifer Yesil, Xuhong Cao, Arvind Rao, Alexander Tsodikov, Moshe Talpaz, Craig E. Cole, Jing C. Ye, Sikander Ailawadhi, Jesus G. Berdeja, Craig C. Hofmeister, Sundar Jagannath, Andrzej Jakubowiak, Amrita Krishnan, Shaji Kumar, Moshe Yair Levy, Sagar Lonial, Gregory J. Orloff, David Siegel, Suzanne Trudel, Saad Z. Usmani, Ravi Vij, Jeffrey L. Wolf, Jeffrey A. Zonder, P. Leif Bergsagel, Daniel Auclair, Hearn Jay Cho, Dan R. Robinson & Arul M. Chinnaiyan. (2022) The genetic heterogeneity and drug resistance mechanisms of relapsed refractory multiple myeloma. Nature Communications 13:1.
Crossref
Crossref
Lea Maria Merz, Florian Buerger, Niels Ziegelasch, Martin Zenker, Ilse Wieland, Tobias Lipek, Tillmann Wallborn, Nicolas Terliesner, Freerk Prenzel, Manuela Siekmeyer & Katalin Dittrich. (2022) A Case Report: First Long-Term Treatment With Burosumab in a Patient With Cutaneous-Skeletal Hypophosphatemia Syndrome. Frontiers in Endocrinology 13.
Crossref
Crossref
Aude Beyens, Laure Dequeker, Hilde Brems, Sandra Janssens, Hannes Syryn, Anne D’Hooghe, Pascale De Paepe, Lieve Vanwalleghem, Annelies Stockman, Elena Vankwikelberge, Sofie De Schepper, Marleen Goeteyn, Patricia Delbeke & Bert Callewaert. (2022) Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies. International Journal of Molecular Sciences 23:7, pages 4036.
Crossref
Crossref
Hoi-Lam Ngan, Chun-Ho Law, Yannie Chung Yan Choi, Jenny Yu-Sum Chan & Vivian Wai Yan Lui. (2022) Precision drugging of the MAPK pathway in head and neck cancer. npj Genomic Medicine 7:1.
Crossref
Crossref
Katie E. Hebron, Edjay Ralph Hernandez & Marielle E. Yohe. (2022) The RASopathies: from pathogenetics to therapeutics. Disease Models & Mechanisms 15:2.
Crossref
Crossref
Jianying Liang, Yifeng Guo, Zhiyong Lu, Hong Yu, Liangcai Wu & Zhirong Yao. (2021)
Woolly hair nevus caused by somatic mutation and Costello syndrome caused by germline mutation in
HRAS
: Consider parental mosaicism in prenatal counseling
. The Journal of Dermatology 49:1, pages 161-164.
Crossref
Crossref
Aparna Palit & Arun C. Inamadar. (2021) RASopathies: Dermatologists’ viewpoints. Indian Journal of Dermatology, Venereology and Leprology 88, pages 452-463.
Crossref
Crossref
Saloni Kapoor, Hannah L. Scanga, Miguel Reyes‐Múgica & Ken K. Nischal. (2021)
Somatic
KRAS
mutation affecting codon 146 in linear sebaceous nevus syndrome
. American Journal of Medical Genetics Part A 185:12, pages 3825-3830.
Crossref
Crossref
Vanessa Franziska Schmidt, Ilse Wieland, Walter A. Wohlgemuth, Jens Ricke, Moritz Wildgruber & Martin Zenker. (2021)
Mosaic
RASopathy
due to
KRAS
variant
G12D
with segmental overgrowth and associated peripheral vascular malformations
. American Journal of Medical Genetics Part A 185:10, pages 3122-3128.
Crossref
Crossref
Shahad Salman, Waseem Fathalla & Hiba Akbari. (2021) Linear Nevus Sebaceous Syndrome in a Child With Infantile Spasms and Focal Cortical Dysplasia. Cureus.
Crossref
Crossref
Caitlin A. Chang, Renee Perrier, Kyle C. Kurek, Juvianee Estrada‐Veras, Anna Lehman, Stephen Yip, Glenda Hendson, Carol Diamond, Jason W. Pinchot, Jennifer M. Tran, Lisa M. Arkin, Beth A. Drolet, Melanie P. Napier, Sarah A. O'Neill, Tugce B. Balci & Kim M. Keppler‐Noreuil. (2021)
Novel findings and expansion of phenotype in a mosaic
RASopathy
caused by somatic
KRAS
variants
. American Journal of Medical Genetics Part A 185:9, pages 2829-2845.
Crossref
Crossref
Aubrey Milunsky & Jeff M. MilunskyJeff M. Milunsky. 2021. Genetic Disorders and the Fetus. Genetic Disorders and the Fetus
572
610
.
Javier-Fernando Montero-Bullón, Óscar González-Velasco, María Isidoro-García & Jesus Lacal. (2021) Integrated in silico MS-based phosphoproteomics and network enrichment analysis of RASopathy proteins. Orphanet Journal of Rare Diseases 16:1.
Crossref
Crossref
Jonathan C Slack, Marie-Anne Bründler, Caitlin A Chang, Renee Perrier, Lucie Lafay-Cousin & Kyle C Kurek. (2021) Bilateral Nephroblastic Tumors and a Complex Renal Vascular Anomaly in a Patient With a Mosaic RASopathy: Novel Histopathologic Features and Molecular Insights. Pediatric and Developmental Pathology 24:3, pages 235-240.
Crossref
Crossref
Noureddine Boukhatem. 2021. Constitutional Oncogenetics. Constitutional Oncogenetics
221
243
.
Tirtha K. Das, Jared Gatto, Rupa Mirmira, Ethan Hourizadeh, Dalia Kaufman, Bruce D. Gelb & Ross Cagan. (2021) Drosophila RASopathy models identify disease subtype differences and biomarkers of drug efficacy. iScience 24:4, pages 102306.
Crossref
Crossref
Jacob J. Adashek, Shumei Kato, Scott M. Lippman & Razelle Kurzrock. (2020) The paradox of cancer genes in non-malignant conditions: implications for precision medicine. Genome Medicine 12:1.
Crossref
Crossref
Heather B. Radtke, Leah E. Lalor, Donald G. Basel & Dawn H. Siegel. (2020) Clinical Implications of Mosaicism and Low-Level Mosaicism in Neurocutaneous Disorders. Current Genetic Medicine Reports 8:4, pages 132-139.
Crossref
Crossref
Alejandra Gadea, Inmaculada Hernández-Muñoz, Asunción Vicente, Evelyn Andrades, Miriam García-Calvente, Laura Camacho, Conchi Fernandez-Rodríguez, Beatriz Bellosillo, Ramon Pujol & Agustín Toll. (2020) Molecular characterisation of oncogenic urothelial mosaic mutations in patients with extensive keratinocytic epidermal naevi. Journal of Medical Genetics 57:9, pages 601-604.
Crossref
Crossref
Elise Y. Cai, Megan N. Kufeld, Samantha Schuster, Sonali Arora, Madeline Larkin, Alexandre A. Germanos, Andrew C. Hsieh & Slobodan Beronja. (2020) Selective Translation of Cell Fate Regulators Mediates Tolerance to Broad Oncogenic Stress. Cell Stem Cell 27:2, pages 270-283.e7.
Crossref
Crossref
Pau Castel, Katherine A. Rauen & Frank McCormick. (2020) The duality of human oncoproteins: drivers of cancer and congenital disorders. Nature Reviews Cancer 20:7, pages 383-397.
Crossref
Crossref
A. A. Orlova, E. L. Dadali & A. V. Polyakov. (2020) Clinical and Genetic Characteristics of Noonan Syndrome and Noonan-like Diseases. Russian Journal of Genetics 56:5, pages 540-547.
Crossref
Crossref
Ute Moog, Ute Felbor, Cristina Has & Birgit Zirn. (2020) Disorders Caused by Genetic Mosaicism. Deutsches Ärzteblatt international.
Crossref
Crossref
Leon P. Bignold. 2020. Principles of Tumors. Principles of Tumors
105
144
.
Mwe Mwe Chao, Martin Zenker & Christian Peter Kratz. 2020. Multidisciplinary Approach to Neurofibromatosis Type 1. Multidisciplinary Approach to Neurofibromatosis Type 1
249
260
.
Leopold M. Groesser & Christian Hafner. 2019. Harper's Textbook of Pediatric Dermatology. Harper's Textbook of Pediatric Dermatology
1260
1275
.
Gema Gordo, Lara Rodriguez-Laguna, Noelia Agra, Pilar Mendez, Marta Feito, Pablo Lapunzina, Juan C. Lopez-Gutierrez & Victor Martinez-Glez. (2019)
Constitutional mosaicism in
RASA1
-related capillary malformation-arteriovenous malformation
. Clinical Genetics 95:4, pages 516-519.
Crossref
Crossref
Lei Chen, Liqin Zhai, Lika'a Fasih Y. Al-Kzayer, Shamil Naji Sarsam, Tingting Liu, Riyadh H. Alzakar & Yozo Nakazawa. (2019) Neurocutaneous Melanosis in Association With Large Congenital Melanocytic Nevi in Children: A Report of 2 Cases With Clinical, Radiological, and Pathogenetic Evaluation. Frontiers in Neurology 10.
Crossref
Crossref
Misako Nagatsuma, Kei Takasawa, Takeru Yamauchi, Ryuichi Nakagawa, Tomoko Mizuno, Eriko Tanaka, Kouhei Yamamoto, Noriko Uemura, Kenichi Kashimada & Tomohiro Morio. (2018) A postzygotic KRAS mutation in a patient with Schimmelpenning syndrome presenting with lipomatosis, renovascular hypertension, and diabetes mellitus. Journal of Human Genetics 64:2, pages 177-181.
Crossref
Crossref
Razia Rahman, Isha Sharma, Lokesh K. Gahlot & Yasha Hasija. (2018) DermaGene and VitmiRS: a comprehensive systems analysis of genetic dermatological disorders. Biomedical Dermatology 2:1.
Crossref
Crossref
M. Prieto-Barrios, R. Llamas-Martin, V. Velasco-Tamariz, A. Calleja-Algarra, Y. Ruano, P.L. Ortiz-Romero & J.L. Rodriguez-Peralto. (2018)
Phacomatosis pigmentokeratotica: a case of
HRAS
mosaicism causing rhabdomyosarcoma
. British Journal of Dermatology 179:5, pages 1163-1167.
Crossref
Crossref
Laura M. McDonell, Gordon Ka-Chun Leung, Hussein Daoud, Janice Ip, Stella Chim, Ho Ming Luk, Lawrence Lan, Kym M. Boycott & Brian Hon-Yin Chung. (2018)
Mosaic
KRAS
mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension
. American Journal of Medical Genetics Part A 176:11, pages 2523-2527.
Crossref
Crossref
Faizan Alawi. (2018) A call to study orphan diseases. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 126:2, pages 95-97.
Crossref
Crossref
F. Sharouf, M. Zaben, A. Lammie, P. Leach & M. I. Bhatti. (2018) Neurocutaneous melanosis presenting with hydrocephalus and malignant transformation: case-based update. Child's Nervous System 34:8, pages 1471-1477.
Crossref
Crossref
Caitlin Porubsky, Jamie K. Teer, Yonghong Zhang, Maria Deschaine, Vernon K. Sondak & Jane L. Messina. (2018) Genomic analysis of a case of agminated Spitz nevi and congenital-pattern nevi arising in extensive nevus spilus. Journal of Cutaneous Pathology 45:2, pages 180-183.
Crossref
Crossref
Young H. Lim, Zoe MoscatoKeith A. Choate. (2017) Mosaicism in Cutaneous Disorders. Annual Review of Genetics 51:1, pages 123-141.
Crossref
Crossref
Mitchell J Machiela, Lea Jessop, Weiyin Zhou, Meredith Yeager & Stephen J Chanock. (2017) Characterization of breakpoint regions of large structural autosomal mosaic events. Human Molecular Genetics 26:22, pages 4388-4394.
Crossref
Crossref
Deborah Saraggi, Roberto Salmaso, Elisa Valentini, Giada Munari, Vincenzo Vindigni, Massimo Rugge, Matteo Fassan & Lorenzo Cerroni. (2017) Pigmented trichoblastoma developed in a sebaceous nevus: HRAS mutation as a common molecular driver. Pathology - Research and Practice 213:7, pages 860-862.
Crossref
Crossref
Maria De Santis, Valentina Sala, Miriam Martini, Giovanni Ferrero & Emilio Hirsch. (2017) PI3K Signaling in Tissue Hyper-Proliferation: From Overgrowth Syndromes to Kidney Cysts. Cancers 9:12, pages 30.
Crossref
Crossref
Mitchell J Machiela & Stephen J Chanock. (2017) The ageing genome, clonal mosaicism and chronic disease. Current Opinion in Genetics & Development 42, pages 8-13.
Crossref
Crossref
Alessandro Corsi, Cristina Remoli, Mara Riminucci, Ernesto Ippolito & John Dimitriou. (2016) A unique case of multiple non-ossifying fibromas with polyostotic monomelic distribution and aggressive clinical course. Skeletal Radiology 46:2, pages 233-236.
Crossref
Crossref
Rocio Acuna-Hidalgo, Joris A. Veltman & Alexander Hoischen. (2016) New insights into the generation and role of de novo mutations in health and disease. Genome Biology 17:1.
Crossref
Crossref
Giulia Angelino, Maria Debora De Pasquale, Luigi De Sio, Annalisa Serra, Luca Massimi, Rita De Vito, Antonio Marrazzo, Laura Lancella, Andrea Carai, Manila Antonelli, Felice Giangaspero, Marco Gessi, Laura Menchini, Laura Scarciolla, Daniela Longo & Angela Mastronuzzi. (2016) NRASQ61K mutated primary leptomeningeal melanoma in a child: case presentation and discussion on clinical and diagnostic implications. BMC Cancer 16:1.
Crossref
Crossref
Florence Le Calvez-Kelm, Matthieu Foll, Magdalena B. Wozniak, Tiffany M. Delhomme, Geoffroy Durand, Priscilia Chopard, Maroulio Pertesi, Eleonora Fabianova, Zora Adamcakova, Ivana Holcatova, Lenka Foretova, Vladimir Janout, Maxime P. Vallee, Sabina Rinaldi, Paul Brennan, James D. McKay, Graham B. Byrnes & Ghislaine Scelo. (2016)
KRAS
mutations in blood circulating cell-free DNA: a pancreatic cancer case-control
. Oncotarget 7:48, pages 78827-78840.
Crossref
Crossref
Baheyeldin Salem, Sean Hofherr, Joyce Turner, Leslie Doros & Patroula Smpokou. (2016) Childhood Rhabdomyosarcoma in Association With a RASopathy Clinical Phenotype and Mosaic Germline SOS1 Duplication. Journal of Pediatric Hematology/Oncology 38:8, pages e278-e282.
Crossref
Crossref
Martin Zenker & Kerstin Kutsche. (2016) RASopathien. Medizinische Genetik 28:1, pages 15-38.
Crossref
Crossref
Said Farschtschi, Victor-Felix Mautner, Silke Hollants, Christian Hagel, Marijke Spaepen, Christoph Schulte, Eric Legius & Hilde Brems. (2015) Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutation. BMC Medical Genetics 16:1.
Crossref
Crossref
Aubrey Milunsky, Clinton Baldwin & Jeff Milunsky. 2015. Genetic Disorders and the Fetus. Genetic Disorders and the Fetus
380
418
.
C. Hafner. (2015) Naevus spilusNevus spilus. Der Hautarzt 66:5, pages 390-391.
Crossref
Crossref
Heidi V.N. Küsters-Vandevelde, Benno Küsters, Adriana C.H. van Engen-van Grunsven, Patricia J.T.A. Groenen, Pieter Wesseling & Willeke A.M. Blokx. (2015) Primary Melanocytic Tumors of the Central Nervous System: a Review with Focus on Molecular Aspects. Brain Pathology 25:2, pages 209-226.
Crossref
Crossref
Mitchell J. Machiela, Weiyin Zhou, Joshua N. Sampson, Michael C. Dean, Kevin B. Jacobs, Amanda Black, Louise A. Brinton, I-Shou Chang, Chu Chen, Constance Chen, Kexin Chen, Linda S. Cook, Marta Crous Bou, Immaculata De Vivo, Jennifer Doherty, Christine M. Friedenreich, Mia M. Gaudet, Christopher A. Haiman, Susan E. Hankinson, Patricia Hartge, Brian E. Henderson, Yun-Chul Hong, H. Dean HosgoodIIIIII, Chao A. Hsiung, Wei Hu, David J. Hunter, Lea Jessop, Hee Nam Kim, Yeul Hong Kim, Young Tae Kim, Robert Klein, Peter Kraft, Qing Lan, Dongxin Lin, Jianjun Liu, Loic Le Marchand, Xiaolin Liang, Jolanta Lissowska, Lingeng Lu, Anthony M. Magliocco, Keitaro Matsuo, Sara H. Olson, Irene Orlow, Jae Yong Park, Loreall Pooler, Jennifer Prescott, Radhai Rastogi, Harvey A. Risch, Fredrick Schumacher, Adeline Seow, Veronica Wendy Setiawan, Hongbing Shen, Xin Sheng, Min-Ho Shin, Xiao-Ou Shu, David VanDen Berg, Jiu-Cun Wang, Nicolas Wentzensen, Maria Pik Wong, Chen Wu, Tangchun Wu, Yi-Long Wu, Lucy Xia, Hannah P. Yang, Pan-Chyr Yang, Wei Zheng, Baosen Zhou, Christian C. Abnet, Demetrius Albanes, Melinda C. Aldrich, Christopher Amos, Laufey T. Amundadottir, Sonja I. Berndt, William J. Blot, Cathryn H. Bock, Paige M. Bracci, Laurie Burdett, Julie E. Buring, Mary A. Butler, Tania Carreón, Nilanjan Chatterjee, Charles C. Chung, Michael B. Cook, Michael Cullen, Faith G. Davis, Ti Ding, Eric J. Duell, Caroline G. Epstein, Jin-Hu Fan, Jonine D. Figueroa, Joseph F. FraumeniJr.Jr., Neal D. Freedman, Charles S. Fuchs, Yu-Tang Gao, Susan M. Gapstur, Ana Patiño-Garcia, Montserrat Garcia-Closas, J. Michael Gaziano, Graham G. Giles, Elizabeth M. Gillanders, Edward L. Giovannucci, Lynn Goldin, Alisa M. Goldstein, Mark H. Greene, Goran Hallmans, Curtis C. Harris, Roger Henriksson, Elizabeth A. Holly, Robert N. Hoover, Nan Hu, Amy Hutchinson, Mazda Jenab, Christoffer Johansen, Kay-Tee Khaw, Woon-Puay Koh, Laurence N. Kolonel, Charles Kooperberg, Vittorio Krogh, Robert C. Kurtz, Andrea LaCroix, Annelie Landgren, Maria Teresa Landi, Donghui Li, Linda M. Liao, Nuria Malats, Katherine A. McGlynn, Lorna H. McNeill, Robert R. McWilliams, Beatrice S. Melin, Lisa Mirabello, Beata Peplonska, Ulrike Peters, Gloria M. Petersen, Ludmila Prokunina-Olsson, Mark Purdue, You-Lin Qiao, Kari G. Rabe, Preetha Rajaraman, Francisco X. Real, Elio Riboli, Benjamín Rodríguez-Santiago, Nathaniel Rothman, Avima M. Ruder, Sharon A. Savage, Ann G. Schwartz, Kendra L. Schwartz, Howard D. Sesso, Gianluca Severi, Debra T. Silverman, Margaret R. Spitz, Victoria L. Stevens, Rachael Stolzenberg-Solomon, Daniel Stram, Ze-Zhong Tang, Philip R. Taylor, Lauren R. Teras, Geoffrey S. Tobias, Kala Viswanathan, Sholom Wacholder, Zhaoming Wang, Stephanie J. Weinstein, William Wheeler, Emily White, John K. Wiencke, Brian M. Wolpin, Xifeng Wu, Jay S. Wunder, Kai Yu, Krista A. Zanetti, Anne Zeleniuch-Jacquotte, Regina G. Ziegler, Mariza de Andrade, Kathleen C. Barnes, Terri H. Beaty, Laura J. Bierut, Karl C. Desch, Kimberly F. Doheny, Bjarke Feenstra, David Ginsburg, John A. Heit, Jae H. Kang, Cecilia A. Laurie, Jun Z. Li, William L. Lowe, Mary L. Marazita, Mads Melbye, Daniel B. Mirel, Jeffrey C. Murray, Sarah C. Nelson, Louis R. Pasquale, Kenneth Rice, Janey L. Wiggs, Anastasia Wise, Margaret Tucker, Luis A. Pérez-Jurado, Cathy C. Laurie, Neil E. Caporaso, Meredith Yeager & Stephen J. Chanock. (2015) Characterization of Large Structural Genetic Mosaicism in Human Autosomes. The American Journal of Human Genetics 96:3, pages 487-497.
Crossref
Crossref
Suguna R. Krishnaswami, Shantanu Kumar, Phillip Ordoukhanian & Benjamin D. Yu. (2015) Fate and Plasticity of the Epidermis in Response to Congenital Activation of BRAF. Journal of Investigative Dermatology 135:2, pages 481-489.
Crossref
Crossref
Jessica C. Hassel, Leopold Groesser, Eva Herschberger, Wilko Weichert & Christian Hafner. (2015) RAS Mutations in Benign Epithelial Tumors Associated with BRAF Inhibitor Treatment of Melanoma. Journal of Investigative Dermatology 135:2, pages 636-639.
Crossref
Crossref
Leon P. Bignold. 2015. Principles of Tumors. Principles of Tumors
185
208
.
Adriana C. H. van Engen-van Grunsven, Heidi Kusters-Vandevelde, Patricia J. T. A. Groenen & Willeke A. M. Blokx. (2014) Update on Molecular Pathology of Cutaneous Melanocytic Lesions: What is New in Diagnosis and Molecular Testing for Treatment?. Frontiers in Medicine 1.
Crossref
Crossref
Rami N. Al-Rohil, David Leung & J. Andrew Carlson. (2014) Congenital vulnerability of cutaneous segments arising from skin mosaicism: A genetic basis for locus minoris resistentiae. Clinics in Dermatology 32:5, pages 577-591.
Crossref
Crossref
C. Hafner, H. Hafner & L. Groesser. (2014) Genetische Grundlagen seborrhoischer Keratosen und epidermaler NäviGenetic basis of seborrheic keratosis and epidermal nevi. Der Pathologe 35:5, pages 413-423.
Crossref
Crossref
Kavita Y. Sarin, Jennifer M. McNiff, Shirley Kwok, Jinah Kim & Paul A. Khavari. (2014) Activating HRAS Mutation in Nevus Spilus. Journal of Investigative Dermatology 134:6, pages 1766-1768.
Crossref
Crossref
Nazneen Rahman. (2014) Realizing the promise of cancer predisposition genes. Nature 505:7483, pages 302-308.
Crossref
Crossref
Pablo Lapunzina, Rocío Ortiz López, Lara Rodríguez-Laguna, Purificación García-Miguel, Augusto Rojas Martínez & Víctor Martínez-Glez. (2014) Impact of NGS in the medical sciences: genetic syndromes with an increased risk of developing cancer as an example of the use of new technologies. Genetics and Molecular Biology 37:1 suppl 1, pages 241-249.
Crossref
Crossref
Efrén Martínez‐Quintana & Fayna Rodríguez‐González. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.
Mitchell J. Machiela & Stephen J. Chanock. (2013) Detectable Clonal Mosaicism in the Human Genome. Seminars in Hematology 50:4, pages 348-359.
Crossref
Crossref
Leopold Groesser, Eva Herschberger, Ana Sagrera, Tor Shwayder, Katharina Flux, Laura Ehmann, Andreas Wollenberg, Antonio Torrelo, Lorea Bagazgoitia, Blanca Diaz-Ley, Sigrid Tinschert, Ilske Oschlies, Sebastian Singer, Marion Mickler, Agusti Toll, Michael Landthaler, Francisco X. Real & Christian Hafner. (2013) Phacomatosis Pigmentokeratotica Is Caused by a Postzygotic HRAS Mutation in a Multipotent Progenitor Cell. Journal of Investigative Dermatology 133:8, pages 1998-2003.
Crossref
Crossref