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American Journal of Medical Genetics. Part A|April 2, 2010
Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3Melissa Leyva-Vega, Jennifer Gerfen, Brian D Thiel, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 21, 2014
Linked Sex Differences in Cognition and Functional Connectivity in YouthTheodore D Satterthwaite, Daniel H Wolf, David R Roalf, et al.
The Journal of Clinical Endocrinology and Metabolism|February 28, 2019
Characterization of Rare Variants in MC4R in African American and Latino Children With Severe Early-Onset ObesityMaria Caterina De Rosa, Alessandra Chesi, Shana McCormack, et al.
Plos Genetics|May 26, 2017
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastomaLee D McDaniel, Karina L Conkrite, Xiao Chang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2023
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic reviewSajjad Biglari, Atefeh Sohanforooshan Moghaddam, Mohammad Amin Tabatabaiefar, et al.
Heart Rhythm|November 2, 2013
Gene expression and genetic variation in human atriaHonghuang Lin, Elena V Dolmatova, Michael P Morley, et al.
Translational Psychiatry|January 22, 2021
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disordersXueming Yao, Joseph T Glessner, Junyi Li, et al.
Bone|December 16, 2014
The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesisFederica Sgariglia, Elena Pedrini, Jonathan P Bradfield, et al.
Molecular Genetics and Metabolism|June 6, 2008
Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: a role for detailed molecular analysis in complex presentations of classical diseasesMatthew A Deardorff, Himabindu Gaddipati, Paige Kaplan, et al.
Human Genomics|November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.
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