2010 - Fellow, The World Academy of Sciences
Genetics, Single-nucleotide polymorphism, Schizophrenia, Allele and Haplotype are her primary areas of study. Her study connects Psychosis and Genetics. Her work in Single-nucleotide polymorphism addresses subjects such as GRIN1, which are connected to disciplines such as SNP genotyping.
Her research integrates issues of Internal medicine and Case-control study in her study of Schizophrenia. Her research on Allele focuses in particular on Polymorphism. Her work in Haplotype addresses issues such as Locus, which are connected to fields such as Chromosome.
Lin He mainly focuses on Genetics, Condensed matter physics, Single-nucleotide polymorphism, Allele and Haplotype. Her research in Genetics intersects with topics in Psychosis and Schizophrenia. She interconnects Bilayer graphene, Graphene and Electron in the investigation of issues within Condensed matter physics.
As a part of the same scientific study, Lin He usually deals with the Single-nucleotide polymorphism, concentrating on Internal medicine and frequently concerns with Pharmacology. Her Allele research is multidisciplinary, relying on both Odds ratio, Endocrinology and Genotype. Her study in Haplotype is interdisciplinary in nature, drawing from both Genetic linkage and Locus.
Her primary areas of investigation include Condensed matter physics, Graphene, Scanning tunneling microscope, Bilayer graphene and Single-nucleotide polymorphism. Her Condensed matter physics research integrates issues from Electron, Fermi level, Magnetic field and Landau quantization. The various areas that Lin He examines in her Graphene study include Quantum dot, Magnetism, Superlattice and Scanning tunneling spectroscopy.
Her Single-nucleotide polymorphism research incorporates themes from Internal medicine and Allele. Her Allele study introduces a deeper knowledge of Genetics. Her study looks at the relationship between Genetics and fields such as Case-control study, as well as how they intersect with chemical problems.
The scientist’s investigation covers issues in Graphene, Condensed matter physics, Scanning tunneling microscope, Landau quantization and Magnetic field. Her Graphene research is multidisciplinary, incorporating elements of Hydrogen, Electronic structure, Superconductivity, Quantum tunnelling and Superlattice. In her research, Density functional theory, Vacancy defect and Quasiparticle is intimately related to Electron, which falls under the overarching field of Quantum tunnelling.
Her studies deal with areas such as Bilayer graphene and Fermi level as well as Condensed matter physics. She has included themes like Atomic units and Dirac fermion in her Scanning tunneling microscope study. The concepts of her Magnetic field study are interwoven with issues in Field pattern, Gaussian, Magnet and Voltage.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci.
Yong Yong Shi;Lin He.
Cell Research (2005)
The sequence and de novo assembly of the giant panda genome
Ruiqiang Li;Wei Fan;Geng Tian;Hongmei Zhu.
Nature (2010)
Identification of loci associated with schizophrenia by genome-wide association and follow-up
Michael C. O'Donovan;Nicholas Craddock;Nadine Norton;Hywel Williams.
Nature Genetics (2008)
Rates of adult schizophrenia following prenatal exposure to the Chinese famine of 1959-1961
David St Clair;Mingqing Xu;Peng Wang;Yaqin Yu.
JAMA (2005)
Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD)
Dawei Li;Pak C. Sham;Pak C. Sham;Michael J. Owen;Lin He;Lin He.
Human Molecular Genetics (2006)
Sclerostin Mediates Bone Response to Mechanical Unloading Through Antagonizing Wnt/β‐Catenin Signaling
Chuwen Lin;Xuan Jiang;Zhongquan Dai;Xizhi Guo.
Journal of Bone and Mineral Research (2009)
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Zi-Jiang Chen;Han Zhao;Lin He;Lin He;Lin He;Yuhua Shi.
Nature Genetics (2011)
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Yongyong Shi;Han Zhao;Yuhua Shi;Yunxia Cao.
Nature Genetics (2012)
Chiral N-Heterocyclic Carbene Catalyzed Staudinger Reaction of Ketenes with Imines: Highly Enantioselective Synthesis of N-Boc β-Lactams
Yan-Rong Zhang;Lin He;Xu Wu;Pan-Lin Shao.
Organic Letters (2008)
Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia.
Dawei Li;David A. Collier;Lin He.
Human Molecular Genetics (2006)
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