Suchergebnisse - "Guo, Tingwei"

PubPharm (88)

31

HLA-B*07, HLA-DRB1*07, HLA-DRB1*12, and HLA-C*03:02 Strongly Associate With BMI : Data From 1.3 Million Healthy Chinese Adults

enthalten in: Diabetes | 2018

von Shen, J. | Guo, T. | Wang, T. | +48

32

Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2

enthalten in: Human molecular genetics | 2018

von Guo, T. | Diacou, A. | Nomaru, H. | +28

33

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

enthalten in: The American journal of psychiatry | 2017

von Bassett, A. | Lowther, C. | Merico, D. | +48

CommentIn: Am J Psychiatry. 2017 Nov 1;174(11):1027-1029. - PMID 29088933

34

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

enthalten in: Circulation. Cardiovascular genetics | 2017

von Guo, T. | Repetto, G. | McDonald McGinn, D. | +44

CommentIn: Circ Cardiovasc Genet. 2017 Oct;10(5):. - PMID 29025762

35

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements

enthalten in: American journal of human genetics | 2017

von Demaerel, W. | Hestand, M. | Vergaelen, E. | +89

RetractionIn: Am J Hum Genet. 2018 Sep 6;103(3):457. - PMID 30193139

36

Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome

enthalten in: PLoS genetics | 2017

von Racedo, S. | Hasten, E. | Lin, M. | +6

37

Expression and regulation of ATL9, an E3 ubiquitin ligase involved in plant defense

enthalten in: PloS one | 2017

von Deng, F. | Guo, T. | Lefebvre, M. | +6

38

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

enthalten in: The American journal of psychiatry | 2017

von Bassett, A. | Lowther, C. | Merico, D. | +47

39

Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits

enthalten in: Aging cell | 2016

von Teumer, A. | Qi, Q. | Nethander, M. | +85

ErratumIn: Aging Cell. 2017 Aug;16(4):898. - PMID 28699312

40

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

enthalten in: Human genetics | 2016

von Mlynarski, E. | Xie, M. | Taylor, D. | +29