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Annals of Neurology|March 3, 2015
Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromesEva M Reinthaler, Borislav Dejanovic, Dennis Lal, et al.Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.Plos One|November 1, 2018
Exome sequencing in large, multiplex bipolar disorder families from CubaAnna Maaser, Andreas J Forstner, Jana Strohmaier, et al.Nature Genetics|June 30, 2015
Mutational dynamics between primary and relapse neuroblastomasAlexander Schramm, Johannes Köster, Yassen Assenov, et al.Human Mutation|July 5, 2022
WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephalyNina Bögershausen, Hannah E Krawczyk, Rami A Jamra, et al.American Journal of Human Genetics|September 2, 2008
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment traitJeroen R Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, et al.Genome Medicine|March 19, 2020
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disordersDennis Lal, Patrick May, Eduardo Perez-Palma, et al.Blood|October 5, 2018
IG-<i>MYC</i> <sup>+</sup> neoplasms with precursor B-cell phenotype are molecularly distinct from Burkitt lymphomasRabea Wagener, Cristina López, Kortine Kleinheinz, et al.Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|June 24, 2015
Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer PatientsKatharina König, Martin Peifer, Jana Fassunke, et al.Journal of Medical Genetics|April 14, 2019
Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883)Jan Hauke, Eric Hahnen, Stephanie Schneider, et al.Pageof 52