Active: Front Cell Dev Biol Clear all

GWAS 2022-12-08

Integrated genomic analysis identifies novel low-frequency cis-regulatory variant rs2279658 associated with VSD risk in Chinese children.

Jin L

Front Cell Dev Biol

Complex ventricular septal defect

180

Participants

N/A

Studies

Details PubMed

GWAS 2022-07-15

Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses.

Huang Y, Liu Y et al.

Front Cell Dev Biol

Aim: Genome-wide association studies (GWAS) analyses have revealed genetic evidence of bipolar disor...

Bipolar disorder type I or bipolar disorder type II (pleiotropy)

845894

Participants

N/A

Studies

Details PubMed

GWAS 2022-02-10

Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk.

Carlson JC, Shaffer JR et al.

Front Cell Dev Biol

Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect, affecting ap...

Orofacial cleft x maternal alcohol consumption interaction (2df)

538

Participants

N/A

Studies

Details PubMed

GWAS 2021-04-16

Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.

Zhang W, Venkataraghavan S et al.

Front Cell Dev Biol

Two large studies of case-parent trios ascertained through a proband with a non-syndromic orofacial ...

Orofacial cleft x maternal periconceptional smoking interaction (1df)

8925

Participants

N/A

Studies

Details PubMed

GWAS 2021-04-09

Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.

Mukhopadhyay N, Feingold E et al.

Front Cell Dev Biol

Orofacial clefts (OFCs) are among the most prevalent craniofacial birth defects worldwide and create...

Nonsyndromic cleft lip with or without cleft palate

9447

Participants

N/A

Studies

Details PubMed

GWAS 2021-03-18

Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.

Cai R, Dong Y et al.

Front Cell Dev Biol

SAPHO syndrome is a rare chronic inflammatory disease which is characterized by the comprehensive ma...

SAPHO syndrome

170

Participants

N/A

Studies

Details PubMed

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Integrated genomic analysis identifies novel low-frequency cis-regulatory variant rs2279658 associated with VSD risk in Chinese children.

Jin L

Front Cell Dev Biol

Complex ventricular septal defect

2022-12-08

Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses.

Huang Y, Liu Y et al.

Front Cell Dev Biol

Bipolar disorder type I or bipolar disorder type II (pleiotropy)

2022-07-15

Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk.

Carlson JC, Shaffer JR et al.

Front Cell Dev Biol

Orofacial cleft x maternal alcohol consumption interaction (2df)

2022-02-10

Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.

Zhang W, Venkataraghavan S et al.

Front Cell Dev Biol

Orofacial cleft x maternal periconceptional smoking interaction (1df)

2021-04-16

Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.

Mukhopadhyay N, Feingold E et al.

Front Cell Dev Biol

Nonsyndromic cleft lip with or without cleft palate

2021-04-09

Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.

Cai R, Dong Y et al.

Front Cell Dev Biol

SAPHO syndrome

2021-03-18

Health & Traits Publications

Integrated genomic analysis identifies novel low-frequency <i>cis</i>-regulatory variant rs2279658 associated with VSD risk in Chinese children.

Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses.

Genome-wide Interaction Study Implicates <i>VGLL2</i> and Alcohol Exposure and <i>PRL</i> and Smoking in Orofacial Cleft Risk.

Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.

Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.

Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.