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Bai Lin

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American Journal of Human Genetics|January 22, 2013

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.

Human Molecular Genetics|January 2, 2014

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.

Nature Genetics|August 24, 2010

Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54Li-Dong Wang, Fu-You Zhou, Xue-Min Li, et al.

Nature|September 2, 2011

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.

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Search research articles

Showing results (251-260 of 254) with videos related to

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American Journal of Human Genetics|January 22, 2013

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.

Human Molecular Genetics|January 2, 2014

Nature Genetics|August 24, 2010

Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54Li-Dong Wang, Fu-You Zhou, Xue-Min Li, et al.

Nature|September 2, 2011

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.

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