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Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|August 1, 2025
Identifying Risk Factors for Metachronous Colorectal Cancer in Lynch SyndromeRobert Hüneburg, Karolin Weber, Stefan Aretz, et al.JCI Insight|October 5, 2023
Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumorsGhada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, et al.Frontiers in Medicine|April 14, 2022
Identification of 27 Novel Variants in Genes COL4A3, COL4A4, and COL4A5 in Lithuanian Families With Alport SyndromeAgne Cerkauskaite, Judy Savige, Karolina Janonyte, et al.Dementia and Geriatric Cognitive Disorders|May 1, 2008
Risk factors for Alzheimer dementia in a community-based birth cohort at the age of 75 yearsPeter Fischer, Sonja Zehetmayer, Susanne Jungwirth, et al.European Journal of Human Genetics : EJHG|February 18, 2011
De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardationUte Grasshoff, Michael Bonin, Ina Goehring, et al.Environmental Pollution (Barking, Essex : 1987)|March 29, 2023
Gene-environment interaction in the association of residential greenness and 25(OH) vitamin DElisabeth Thiering, Iana Markevych, Sara Kress, et al.Journal of the American Society of Nephrology : JASN|October 6, 2020
Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal AgenesisVeronica Arora, Suliman Khan, Ayman W El-Hattab, et al.Human Molecular Genetics|September 7, 2010
Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasisLena F Burbulla, Carina Schelling, Hiroki Kato, et al.Neurology. Genetics|April 5, 2017
CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposisHolger Hengel, Alex Magee, Muhammad Mahanjah, et al.Cerebral Cortex (New York, N.Y. : 1991)|December 30, 2009
The effects of COMT (Val108/158Met) and DRD4 (SNP -521) dopamine genotypes on brain activations related to valence and magnitude of rewardsEstela Camara, Ulrike M Krämer, Toni Cunillera, et al.Pageof 67