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Dose and time effects of solar‐simulated ultraviolet radiation on the in vivo human skin transcriptome

British journal of dermatology (1951), 2020-06, Vol.182 (6), p.1458-1468

2020

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Origin of Primate Orphan Genes: A Comparative Genomics Approach

Molecular biology and evolution, 2009-03, Vol.26 (3), p.603-612

2009

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Spectrum of clinical heterogeneity of β-tubulin TUBB5 gene mutations

Gene, 2019-05, Vol.695, p.12-17

2019

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太阳紫外线辐射如何影响皮肤基因的研究

British journal of dermatology (1951), 2020-06, Vol.182 (6), p.e204-e204

2020

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A study into how ultraviolet radiation from the sun effects genes in the skin

British journal of dermatology (1951), 2020-06, Vol.182 (6), p.e192-e192

2020

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Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB

Molecular psychiatry, 2009-01, Vol.14 (1), p.71-85

2009

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Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

Translational psychiatry, 2016-03, Vol.6 (3), p.e768-e768

2016

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DNA methylation in neurodegenerative disorders: a missing link between genome and environment?

Clinical genetics, 2011-07, Vol.80 (1), p.1-14

2011

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Next generation diagnostics of cystic fibrosis and CFTR-related disorders by targeted multiplex high-coverage resequencing of CFTR

Journal of medical genetics, 2013-07, Vol.50 (7), p.455-462

2013

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Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

Molecular psychiatry, 2010-10, Vol.15 (10), p.1023-1033

2010

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Met66 in the brain-derived neurotrophic factor (BDNF) precursor is associated with anorexia nervosa restrictive type

Molecular psychiatry, 2003-08, Vol.8 (8), p.745-751

2003

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THU0012 Observing Dysregulation of Signal Transduction Genes in the WNT Pathway Using two Methods

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.197

2015

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Gene-environment interaction in anorexia nervosa: relevance of non-shared environment and the serotonin transporter gene

Molecular psychiatry, 2011-06, Vol.16 (6), p.590-592

2011

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Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiency

Gene, 2015-10, Vol.571 (1), p.52-57

2015

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Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients

Journal of medical genetics, 2003-06, Vol.40 (6), p.e82-82

2003

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X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation

BMC genomics, 2007-11, Vol.8 (1), p.443-443, Article 443

2007

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High risk of lifetime history of suicide attempts among CYP2D6 ultrarapid metabolizers with eating disorders

Molecular psychiatry, 2011-07, Vol.16 (7), p.691-692

2011

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

Nature genetics, 1999-09, Vol.23 (1), p.16-18

1999

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Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis

Leukemia, 2013-12, Vol.27 (12), p.2376-2379

2013

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ADRB2 Gly16Arg polymorphism, asthma control and lung function decline

The European respiratory journal, 2011-11, Vol.38 (5), p.1029-1035

2011

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Alterations of Neocortical Pyramidal Cell Phenotype in the Ts65Dn Mouse Model of Down Syndrome: Effects of Environmental Enrichment

Cerebral cortex (New York, N.Y. 1991), 2003-07, Vol.13 (7), p.758-764

2003

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D184E mutation in aquaporin-4 gene impairs water permeability and links to deafness

Neuroscience, 2011-12, Vol.197, p.80-88

2011

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Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Human genetics, 2000-01, Vol.106 (1), p.40-44

2000

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Additional support for the association of SLITRK1 var321 and Tourette syndrome

Molecular psychiatry, 2010-05, Vol.15 (5), p.447-450

2010

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Variants in estrogen receptor alpha gene are associated with phenotypical expression of obsessive-compulsive disorder

Psychoneuroendocrinology, 2011-05, Vol.36 (4), p.473-483

2011

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Dose and time effects of solar‐simulated ultraviolet radiation on the in vivo human skin transcriptome

Origin of Primate Orphan Genes: A Comparative Genomics Approach

Spectrum of clinical heterogeneity of β-tubulin TUBB5 gene mutations

太阳紫外线辐射如何影响皮肤基因的研究

A study into how ultraviolet radiation from the sun effects genes in the skin

Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB

Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

DNA methylation in neurodegenerative disorders: a missing link between genome and environment?

Next generation diagnostics of cystic fibrosis and CFTR-related disorders by targeted multiplex high-coverage resequencing of CFTR

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

Met66 in the brain-derived neurotrophic factor (BDNF) precursor is associated with anorexia nervosa restrictive type

THU0012 Observing Dysregulation of Signal Transduction Genes in the WNT Pathway Using two Methods

Gene-environment interaction in anorexia nervosa: relevance of non-shared environment and the serotonin transporter gene

Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiency

Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients

X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation

High risk of lifetime history of suicide attempts among CYP2D6 ultrarapid metabolizers with eating disorders

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis

ADRB2 Gly16Arg polymorphism, asthma control and lung function decline

Alterations of Neocortical Pyramidal Cell Phenotype in the Ts65Dn Mouse Model of Down Syndrome: Effects of Environmental Enrichment

D184E mutation in aquaporin-4 gene impairs water permeability and links to deafness

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Additional support for the association of SLITRK1 var321 and Tourette syndrome

Variants in estrogen receptor alpha gene are associated with phenotypical expression of obsessive-compulsive disorder

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