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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 14, 2008
Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic womenBronson E Oosterhuis, K Steven LaForge, Dmitri Proudnikov, et al.
NPJ Parkinson'S Disease|February 10, 2026
Genetic co-regulation of neopterin and Parkinson's diseaseValeria Orrù, Michele Marongiu, Maristella Steri, et al.
BMC Urology|October 23, 2016
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidismYanping Wang, Jin Li, Thomas F Kolon, et al.
The Journal of Investigative Dermatology|November 25, 2003
Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomataAmalia Martinez-Mir, Benjamin Glaser, Gary S Chuang, et al.
BMC Proceedings|December 19, 2009
Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysisSu-Wei Chang, Seung Hoan Choi, Ke Li, et al.
Genetic Epidemiology|October 6, 2005
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mappingNathan A Ellis, Tomas Kirchhoff, Nandita Mitra, et al.
Gastroenterology|July 21, 2015
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel diseaseJudith R Kelsen, Noor Dawany, Christopher J Moran, et al.
Nature Genetics|May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BIan D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
Nature|August 30, 2008
Identification of ALK as a major familial neuroblastoma predisposition geneYaël P Mossé, Marci Laudenslager, Luca Longo, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
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