T32GM008638

NIH – National Institute of General Medical Sciences

Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders

Zhang, X., Lucas, A. M., Veturi, Y., Drivas, T. G., Bone, W. P., Verma, A., Chung, W. K., Crosslin, D., Denny, J. C., Hebbring, S., Jarvik, G. P., Kullo, I., Larson, E. B., Rasmussen-Torvik, L. J., Schaid, D. J., Smoller, J. W., Stanaway, I. B., Wei, W.-Q., Weng, C., & Ritchie, M. D. (2022). Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-30678-w

Authors:

Xinyuan Zhang

Anastasia M Lucas

Yogasudha Veturi

Theodore G Drivas

William P Bone

Anurag Verma

Wendy K Chung

David Crosslin

Joshua C Denny

Scott Hebbring

Gail P Jarvik

Iftikhar Kullo

Eric B Larson

Laura J Rasmussen-Torvik

Daniel J Schaid

Jordan W Smoller

Ian B Stanaway

Wei-Qi Wei

Chunhua Weng

Marylyn D Ritchie

Affiliated Authors:

Wendy K Chung

Chunhua Weng

Columbia Affiliation:

Vagelos College of Physicians and Surgeons

Subjects:

Cardiovascular Diseases (MeSH)

Nervous System Diseases (MeSH)

Grants:

ZIAHG200417 (NIH – National Human Genome Research Institute)

U01HG006379 (NIH – National Human Genome Research Institute)

T32GM008638 (NIH – National Institute of General Medical Sciences)

P50GM115318 (NIH – National Institute of General Medical Sciences)

Publication Type:

Article

Unique ID:

10.1038/s41467-022-30678-w

PMID:

35701404

DOI:

10.1038/s41467-022-30678-w

Journal:

Nature Communications

Publication Date:

2022-06-15

Data Source:

PubMed

Source Link:

View PubMed Record

Record Created:

Thursday, January 16, 2025 - 13:26

Expanding the phenotypic spectrum of ARCN1-related syndrome

Ritter, A. L., Gold, J., Hayashi, H., Ackermann, A. M., Hanke, S., Skraban, C., Cuddapah, S., Bhoj, E., Li, D., Kuroda, Y., Wen, J., Takeda, R., Bibb, A., El Chehadeh, S., Piton, A., Ohl, J., Kukolich, M. K., Nagasaki, K., Kato, K., … Izumi, K. (2022). Expanding the phenotypic spectrum of ARCN1-related syndrome. Genetics in Medicine, 24(6), 1227–1237. https://doi.org/10.1016/j.gim.2022.02.005

Authors:

Alyssa L Ritter

Jessica Gold

Hiroshi Hayashi

Amanda M Ackermann

Stephanie Hanke

Cara Skraban

Sanmati Cuddapah

Elizabeth Bhoj

Dong Li

Yukiko Kuroda

Jessica Wen

Ryojun Takeda

Audrey Bibb

Salima El Chehadeh

Amélie Piton

Jeanine Ohl

Mary K Kukolich

Keisuke Nagasaki

Kohji Kato

Tomoo Ogi

Tricia Bhatti

Pierre Russo

Bryan Krock

Jill R Murrell

Jennifer A Sullivan

Vandana Shashi

Nicholas Stong

Hakon Hakonarson

Kentaro Sawano

Erin Torti

Rebecca Willaert

Yue Si

William Ross Wilcox

Katrine Verena Wirgenes

Kristian Thomassen

Katherine Carlotti

Angelika Erwin

Joanna Lazier

Thorsten Marquardt

Miao He

Andrew C Edmondson

Kosuke Izumi

Affiliated Authors:

Nicholas Stong

Columbia Affiliation:

Institute for Genomic Medicine

Subjects:

Cataract (MeSH)

Dwarfism (MeSH)

Hepatoblastoma (MeSH)

Intellectual Disability (MeSH)

Liver Neoplasms (MeSH)

Micrognathism (MeSH)

Author Keywords:

arcn1

copi

micrognathia