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American Journal of Human Genetics|September 22, 2005
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8qMatthew B McQueen, B Devlin, Stephen V Faraone, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophreniaRunjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.
HGG Advances|August 31, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophreniaRunjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.
Human Molecular Genetics|June 20, 2013
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth diseaseHamid Azzedine, Petra Zavadakova, Violaine Planté-Bordeneuve, et al.
Transboundary and Emerging Diseases|April 20, 2021
Brucellosis in dairy herds: Farm characteristics and practices in relation to likely adoption of three potential private-public partnership (PPP) vaccination control strategies in West and Central AfricaLaura Craighead, Bhagyalakshmi Chengat Prakashbabu, Imadidden Musallam, et al.
Journal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|March 29, 2021
Choroidal Thickness Is a Biomarker Associated With Response to Treatment in Ankylosing SpondylitisMartina Steiner, Maria Del Mar Esteban-Ortega, Israel Thuissard-Vasallo, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Ophthalmology and Therapy|January 22, 2023
Validation of UVEDAI: An Index for Evaluating the Level of Inflammatory Activity in UveitisEsperanza Pato-Cour, Mª Auxiliadora Martin-Martinez, Lara Borrego-Sanz, et al.
Cancers|July 2, 2021
Follow-Up Study Confirms the Presence of Gastric Cancer DNA Methylation Hallmarks in High-Risk Precursor LesionsAntonio Gómez, Miguel L Pato, Luis Bujanda, et al.
Nature Genetics|March 14, 2023
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populationsDongjing Liu, Dara Meyer, Brian Fennessy, et al.
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