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Elife|December 21, 2022
TGF-β signaling and Creb5 cooperatively regulate Fgf18 to control pharyngeal muscle developmentJifan Feng, Xia Han, Yuan Yuan, et al.
Elife|January 22, 2021
Runx2-Twist1 interaction coordinates cranial neural crest guidance of soft palate myogenesisXia Han, Jifan Feng, Tingwei Guo, et al.
Genes|August 6, 2021
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United StatesOmobola O Oluwafemi, Fadi I Musfee, Laura E Mitchell, et al.
Biochemical and Biophysical Research Communications|July 19, 2005
Positive association of the human GABA-A-receptor beta 2 subunit gene haplotype with schizophrenia in the Chinese Han populationJixia Liu, Yongyong Shi, Wei Tang, et al.
Diabetes|October 9, 2013
A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetesRobert L Hanson, Yunhua L Muller, Sayuko Kobes, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 29, 2010
Pharacogenetic effects of dopamine transporter gene polymorphisms on response to chlorpromazine and clozapine and on extrapyramidal syndrome in schizophreniaMingqing Xu, Qinghe Xing, Sheng Li, et al.
Human Mutation|July 29, 2011
Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patientsTingwei Guo, Donna McDonald-McGinn, Anna Blonska, et al.
Human Molecular Genetics|January 24, 2018
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Tingwei Guo, Alexander Diacou, Hiroko Nomaru, et al.
Human Genetics|January 9, 2016
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeElisabeth E Mlynarski, Michael Xie, Deanne Taylor, et al.
American Journal of Medical Genetics. Part A|October 5, 2012
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patientsSean B Herman, Tingwei Guo, Donna M McDonald McGinn, et al.
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