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Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
HGG Adv. 2023 Aug 25;4(4):100234. doi: 10.1016/j.xhgg.2023.100234. eCollection 2023 Oct 12.
HGG Adv. 2023.
PMID: 37719664
Free PMC article.
Integrative analysis of transcriptome dynamics during human craniofacial development identifies candidate disease genes.
Yankee TN, Oh S, Winchester EW, Wilderman A, Robinson K, Gordon T, Rosenfeld JA, VanOudenhove J, Scott DA, Leslie EJ, Cotney J.
Yankee TN, et al.
Nat Commun. 2023 Aug 2;14(1):4623. doi: 10.1038/s41467-023-40363-1.
Nat Commun. 2023.
PMID: 37532691
Free PMC article.
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Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Diaz Perez KK, Chung S, Head ST, Epstein MP, Hecht JT, Wehby GL, Weinberg SM, Murray JC, Marazita ML, Leslie EJ.
Diaz Perez KK, et al.
Am J Med Genet A. 2023 Oct;191(10):2558-2570. doi: 10.1002/ajmg.a.63336. Epub 2023 Jun 23.
Am J Med Genet A. 2023.
PMID: 37350193
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Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.
Diaz Perez KK, Curtis SW, Sanchis-Juan A, Zhao X, Head T, Ho S, Carter B, McHenry T, Bishop MR, Valencia-Ramirez LC, Restrepo C, Hecht JT, Uribe LM, Wehby G, Weinberg SM, Beaty TH, Murray JC, Feingold E, Marazita ML, Cutler DJ, Epstein MP, Brand H, Leslie EJ.
Diaz Perez KK, et al.
Genet Med. 2023 Oct;25(10):100918. doi: 10.1016/j.gim.2023.100918. Epub 2023 Jun 15.
Genet Med. 2023.
PMID: 37330696
Free article.
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Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
Robinson K, Mosley TJ, Rivera-González KS, Jabbarpour CR, Curtis SW, Adeyemo WL, Beaty TH, Butali A, Buxó CJ, Cutler DJ, Epstein MP, Gowans LJ, Hecht JT, Murray JC, Shaw GM, Uribe LM, Weinberg SM, Brand H, Marazita ML, Lipinski RJ, Leslie EJ.
Robinson K, et al.
medRxiv [Preprint]. 2023 Apr 6:2023.03.01.23286642. doi: 10.1101/2023.03.01.23286642.
medRxiv. 2023.
PMID: 37066311
Free PMC article.
Updated.
Preprint.
Item in Clipboard
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Perez KKD, Chung S, Head ST, Epstein MP, Hecht JT, Wehby GL, Weinberg SM, Murray JC, Marazita ML, Leslie EJ.
Perez KKD, et al.
medRxiv [Preprint]. 2023 Feb 7:2023.02.01.23285340. doi: 10.1101/2023.02.01.23285340.
medRxiv. 2023.
PMID: 36798250
Free PMC article.
Updated.
Preprint.
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