Publications by authors named "Michael Sierant"

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Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes.
Michael C Sierant, Sheng Chih Jin, Kaya Bilguvar, Sarah U Morton, Weilai Dong

Proc Natl Acad Sci U S A· April 2025

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Recessive genetic contribution to congenital heart disease in 5,424 probands.
Weilai Dong, Sheng Chih Jin, Michael C Sierant, Ziyu Lu, Boyang Li

Proc Natl Acad Sci U S A· March 2025

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Somatic Mutations in Sporadic Cerebral Cavernous Malformations.
Matthieu Peyre, Danielle Miyagishima, Franck Bielle, Françoise Chapon, Michael Sierant

N Engl J Med· September 2021

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Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, Xue Zeng, Michael C Sierant

Nat Genet· March 2021

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Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.
Sheng Chih Jin, Weilai Dong, Adam J Kundishora, Shreyas Panchagnula, Andres Moreno-De-Luca, Michael C Sierant

Nat Med· November 2020

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Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, Xue Zeng, Michael C Sierant

Nat Genet· October 2020

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Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia.
Weilai Dong, Sheng Chih Jin, August Allocco, Xue Zeng, Amar H Sheth, Michael C Sierant

iScience· October 2020

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Single-Cell Ssequencing in Cancer: Recent Applications to Immunogenomics and Multi-omics Tools.
Michael C Sierant, Jungmin Choi

Genomics Inform· December 2018

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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Michael C Sierant

Nat Genet· November 2017

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Compound loss of function of nuclear receptors Tr2 and Tr4 leads to induction of murine embryonic β-type globin genes.
Shuaiying Cui, Osamu Tanabe, Michael Sierant, Lihong Shi, Andrew Campbell

Blood· February 2015

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