Publications by authors named "Elizabeth Leslie"

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Building a growing genomic repository for maternal and fetal health through the PING Consortium.
Clara M Abdelmalek, Shriya Singh, Blain Fasil, Allison R Horvath, Sarah B Mulkey, Elizabeth J Leslie

Pediatr Res· August 2025

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Identification of functional non-coding variants associated with orofacial cleft.
Priyanka Kumari, Ryan Z Friedman, Lira Pi, Sarah W Curtis, Kitt Paraiso, Elizabeth J Leslie

bioRxiv· February 2025

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Multi-ancestry Genome Wide Association Study Meta-analysis of Non-syndromic Orofacial Clefts.
Zhonglin Jia, Nandita Mukhopadhyay, Zhenglin Yang, Azeez Butali, Jialin Sun, Elizabeth J Leslie

medRxiv· December 2024

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Gene-by-environment interactions involving maternal exposures with orofacial cleft risk in Filipinos.
Zeynep Erdogan-Yildirim, Jenna C Carlson, Nandita Mukhopadhyay, Elizabeth J Leslie, Carmencita Padilla

medRxiv· December 2024

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Genome-wide study of gene-by-sex interactions identifies risks for cleft palate.
Kelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, Terri H Beaty, Azeez Butali, Elizabeth J Leslie

Hum Genet· November 2024

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Genome-wide association studies of Down syndrome associated congenital heart defects.
Elizabeth R Feldman, Yunqi Li, David J Cutler, Tracie C Rosser, Stephanie B Wechsler, Elizabeth J Leslie

medRxiv· September 2024

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Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis.
Caroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, Hemma Murali, Casey Tsimbal, Elizabeth J Leslie

Commun Biol· August 2024

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Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts.
Toshiyuki Itai, Fangfang Yan, Andi Liu, Yulin Dai, Chihiro Iwaya, Elizabeth J Leslie

HGG Adv· July 2024

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Functional analysis of gene variants and isoforms in orofacial cleft pathogenesis.
Caroline Caetano da Silva, Claudio Macias Trevino, Jason Mitchell, Hemma Murali, Casey Tsimbal, Elizabeth J Leslie

bioRxiv· July 2024

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The heterogeneous genetic architectures of orofacial clefts.
Kelsey Robinson, Sarah W Curtis, Elizabeth J Leslie

Trends Genet· May 2024

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Genome-wide study of gene-by-sex interactions identifies risks for cleft palate.
Kelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, Terri H Beaty, Azeez Butali, Elizabeth J Leslie

medRxiv· May 2024

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Building a growing genomic data repository for maternal and fetal health through the PING Consortium.
Clara M Abdelmalek, Shriya Singh, Blain Fasil, Allison R Horvath, Sarah B Mulkey, Elizabeth J Leslie

medRxiv· May 2024

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Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.
Kimberly K Diaz Perez, Sarah W Curtis, Alba Sanchis-Juan, Xuefang Zhao, Taylor Head, Elizabeth J Leslie

Genet Med· October 2023

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Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, Michael P Epstein, Jacqueline T Hecht, Elizabeth J Leslie

Am J Med Genet A· October 2023

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Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Sarah W Curtis, Jenna C Carlson, Terri H Beaty, Jeffrey C Murray, Seth M Weinberg, Elizabeth J Leslie

Hum Genet· October 2023

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Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
Kelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, Christopher R Jabbarpour, Sarah W Curtis, Elizabeth J Leslie

HGG Adv· October 2023

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Integrative analysis of transcriptome dynamics during human craniofacial development identifies candidate disease genes.
Tara N Yankee, Sungryong Oh, Emma Wentworth Winchester, Andrea Wilderman, Kelsey Robinson, Elizabeth J Leslie

Nat Commun· August 2023

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Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
Kelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, Christopher R Jabbarpour, Sarah W Curtis, Elizabeth J Leslie

medRxiv· April 2023

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POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes.
S Taylor Head, Elizabeth J Leslie, David J Cutler, Michael P Epstein

Bioinformatics· April 2023

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Rare genetic variants in modify orofacial cleft phenotypes.
Sarah W Curtis, Jenna C Carlson, Terri H Beaty, Jeffrey C Murray, Seth M Weinberg, Elizabeth J Leslie

medRxiv· March 2023

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Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, Michael P Epstein, Jacqueline T Hecht, Elizabeth J Leslie

medRxiv· February 2023

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Efficient estimation of indirect effects in case-control studies using a unified likelihood framework.
Glen A Satten, Sarah W Curtis, Claudia Solis-Lemus, Elizabeth J Leslie, Michael P Epstein

Stat Med· July 2022

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Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes.
Nandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, George Wehby, Luz Consuelo Valencia-Ramirez, Elizabeth J Leslie

Genet Epidemiol· April 2022

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Genome-wide Interaction Study Implicates and Alcohol Exposure and and Smoking in Orofacial Cleft Risk.
Jenna C Carlson, John R Shaffer, Fred Deleyiannis, Jacqueline T Hecht, George L Wehby, Elizabeth J Leslie

Front Cell Dev Biol· February 2022

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Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate.
Julia Welzenbach, Nigel L Hammond, Miloš Nikolić, Frederic Thieme, Nina Ishorst, Elizabeth J Leslie

HGG Adv· July 2021

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