In his articles, Yin Yao Shugart combines various disciplines, including Genetics and Immunology. He merges Immunology with Genetics in his study. He undertakes interdisciplinary study in the fields of Gene and Mutation through his works. His multidisciplinary approach integrates Internal medicine and Oncology in his work. In his study, he carries out multidisciplinary Oncology and Internal medicine research. He conducted interdisciplinary study in his works that combined Genotype and Genetic association. In his articles, he combines various disciplines, including Genetic association and Genome-wide association study. With his scientific publications, his incorporates both Genome-wide association study and Genetic architecture. He performs integrative study on Genetic architecture and Genotype.
His Genetics study frequently draws connections to adjacent fields such as SNP. His study deals with a combination of Gene and Haplotype. He undertakes multidisciplinary investigations into Haplotype and Single-nucleotide polymorphism in his work. As part of his studies on Single-nucleotide polymorphism, he often connects relevant subjects like SNP. He combines Genotype and Allele in his studies. He applies his multidisciplinary studies on Allele and Genotype in his research. In his study, he carries out multidisciplinary Internal medicine and Oncology research. Yin Yao Shugart performs integrative study on Oncology and Internal medicine. His Psychiatry study frequently draws connections between related disciplines such as Schizophrenia (object-oriented programming).
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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
John D. Rioux;John D. Rioux;Ramnik J. Xavier;Kent D. Taylor;Mark S. Silverberg.
Nature Genetics (2007)
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
Susan E. Hong;Yin Yao Shugart;David T. Huang;Saad Al Shahwan.
Nature Genetics (2000)
Mapping human genetic diversity in Asia
Mahmood Ameen Abdulla;Ikhlak Ahmed;Anunchai Assawamakin;Anunchai Assawamakin;Jong Bhak.
Exome sequencing and the genetic basis of complex traits
Adam Kiezun;Kiran Garimella;Ron Do;Ron Do;Nathan O Stitziel;Nathan O Stitziel.
Nature Genetics (2012)
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.
Russell J Ferland;Wafaa Eyaid;Randall V Collura;Laura D Tully.
Nature Genetics (2004)
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex
Volney L Sheen;Vijay S Ganesh;Meral Topcu;Guillaume Sebire.
Nature Genetics (2004)
Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma
De Ke Jiang;Jielin Sun;Guangwen Cao;Yao Liu.
Nature Genetics (2013)
Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4
Bing Jian Feng;Wei Huang;Yin Yao Shugart;Ming K. Lee.
Nature Genetics (2002)
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS
Mattheisen M;Samuels Jf;Wang Y;Greenberg Bd.
Molecular Psychiatry (2015)
Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
Lea K. Davis;Dongmei Yu;Clare L. Keenan;Eric R. Gamazon.
PLOS Genetics (2013)
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