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Schizophrenia Bulletin|November 10, 2020
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US VeteransTim B Bigdeli, Ayman H Fanous, Yuli Li, et al.Medrxiv : the Preprint Server for Health Sciences|July 7, 2021
Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 lineagesMary E Petrone, Jessica E Rothman, Mallery I Breban, et al.Nature Genetics|October 10, 2017
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probandsSheng Chih Jin, Jason Homsy, Samir Zaidi, et al.Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.Science (New York, N.Y.)|January 26, 2013
Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMOVictoria E Clark, E Zeynep Erson-Omay, Akdes Serin, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|August 21, 2023
The polygenic basis of relapse after a first episode of schizophreniaÀlex-González Segura, Llucia Prohens, Patricia Gassó, et al.Nature|January 24, 2012
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalitiesLynn M Boyden, Murim Choi, Keith A Choate, et al.Communications Biology|May 11, 2022
Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 variants Alpha and IotaMary E Petrone, Jessica E Rothman, Mallery I Breban, et al.American Journal of Human Genetics|November 4, 2017
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney MalformationsSimone Sanna-Cherchi, Kamal Khan, Rik Westland, et al.Pageof 166