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Clinical Epidemiology Volume 10, 2018 - Issue
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Original Research

Parental age and risk of genetic syndromes predisposing to nervous system tumors: nested case–control study

Maral Adel Fahmideh1 Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, SwedenCorrespondence[email protected]
,
Giorgio Tettamanti1 Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden
,
Catharina Lavebratt2 Neurogenetics Unit, Department of Molecular Medicine and Surgery, Karolinska Institutet, Center for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden
,
Mats Talbäck1 Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden
,
Tiit Mathiesen3 Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden;4 University of Copenhagen, Copenhagen, Denmark
,
Birgitta Lannering5 Department of Pediatrics, University of Gothenburg, Gothenburg, Sweden
,
Kimberly J Johnson6 Brown School, Washington University in St Louis, St Louis, MO, USA;7 Department of Pediatrics, School of Medicine, Washington University in St Louis, St Louis, MO, USA
&
Maria Feychting1 Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden
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Pages 729-738 | Published online: 20 Jun 2018

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Giorgio Tettamanti, Hanna Mogensen, Ann Nordgren & Maria Feychting. (2019) Maternal smoking during pregnancy and risk of phacomatoses: results from a Swedish register-based study. Clinical Epidemiology 11, pages 793-800.
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Articles from other publishers (4)

Kimberly J. Johnson, Justin M. Barnes, Arash Delavar, Caitlin P. O’Connell & Xiaoyan Wang. (2023) Facility patient volume and survival among individuals diagnosed with malignant central nervous system tumors. Journal of Neuro-Oncology 161:1, pages 117-126.
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Belen Garcia, Nuria Catasus, Andrea Ros, Inma Rosas, Alejandro Negro, Mercedes Guerrero-Murillo, Ana Maria Valero, Anna Duat-Rodriguez, Juan Luis Becerra, Sandra Bonache, Conxi Lázaro Garcia, Carmina Comas, Isabel Bielsa, Eduard Serra, Concepción Hernández-Chico, Yolanda Martin, Elisabeth Castellanos & Ignacio Blanco. (2022) Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered? . Journal of Medical Genetics 59:10, pages 1017-1023.
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Alessandro Stella, Patrizia Lastella, Luigi Viggiano, Rosanna Bagnulo & Nicoletta Resta. (2022) Clinical presentation and genetic analyses of neurofibromatosis type 1 in independent patients with monoallelic double de novo closely spaced mutations in the NF1 gene . Human Mutation 43:10, pages 1354-1360.
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Matteo Riva, Davide Martorana, Vera Uliana, Edoardo Caleffi, Elena Boschi, Livia Garavelli, Giovanni Ponti, Luca Sangiorgi, Claudio Graziano, Stefania Bigoni, Luca Maria Rocchetti, Simona Madeo, Fiorenza Soli, Enrico Grosso, Diana Carli, Matteo Goldoni, Francesco Pisani & Antonio Percesepe. (2021) Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I . Genes, Chromosomes and Cancer 61:1, pages 10-21.
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