Elizabeth J. Leslie
Emory & Henry College
H-index: 33
North America-United States
Top articles of Elizabeth J. Leslie
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
The heterogeneous genetic architectures of orofacial clefts | Kelsey Robinson Sarah W Curtis Elizabeth J Leslie | 2024/3/13 | |
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes | Human genetics | Sarah W Curtis Jenna C Carlson Terri H Beaty Jeffrey C Murray Seth M Weinberg | 2023/10 |
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference? | American Journal of Medical Genetics Part A | Kimberly K Diaz Perez Sydney Chung S Taylor Head Michael P Epstein Jacqueline T Hecht | 2023/2/7 |
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting | Genetics in Medicine | Kimberly K Diaz Perez Sarah W Curtis Alba Sanchis-Juan Xuefang Zhao Taylor Head | 2023/10/1 |
Integrative analysis of transcriptome dynamics during human craniofacial development identifies candidate disease genes | Nature Communications | Tara N Yankee Sungryong Oh Emma Wentworth Winchester Andrea Wilderman Kelsey Robinson | 2023/8/2 |
Heritable Variation in Lymphocyte-Related Traits and Risk of Down Syndrome Acute Lymphoblastic Leukemia: A Mendelian Randomization Study | Blood | Yunqi Li Melissa A Richard Linda Kachuri Yao Yu Ching-Ju Ruu Hsu | 2023/11/28 |
POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes | Bioinformatics | S Taylor Head Elizabeth J Leslie David J Cutler Michael P Epstein | 2023/4/1 |
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate | Human Genetics and Genomics Advances | Kelsey Robinson Trenell J Mosley Kenneth S Rivera-González Christopher R Jabbarpour Sarah W Curtis | 2023/10/12 |
Rare genetic variants in SEC24D modify orofacial cleft phenotypes | medRxiv | Sarah W Curtis Jenna C Carlson Terri H Beaty Jeffrey C Murray Seth M Weinberg | 2023/3/27 |
Feasibility of social Media recruitment for orofacial cleft genetic research | The Cleft Palate-Craniofacial Journal | Grace Carlock Kelly Manning Elizabeth J Leslie | 2022/6 |
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions | Genetic, Environmental and Synergistic Gene-Environment Contributions to Craniofacial Defects | Noah Lucas Weisleder LVKS Bhaskar Renato Assis Machado Nandita Mukhopadhyay N Mukhopadhyay | 2022/11/8 |
Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes | Genetic epidemiology | Nandita Mukhopadhyay Eleanor Feingold Lina Moreno‐Uribe George Wehby Luz Consuelo Valencia‐Ramirez | 2022/4 |
Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk | Frontiers in cell and developmental biology | Jenna C Carlson John R Shaffer Fred Deleyiannis Jacqueline T Hecht George L Wehby | 2022/2/10 |
Heritability analysis in twins indicates a genetic basis for velopharyngeal morphology | The Cleft Palate-Craniofacial Journal | Myoung Keun Lee Chenxing Liu Elizabeth J Leslie John R Shaffer Jamie L Perry | 2022/11 |
A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic Paraplegia | Movement Disorders | Derek E Neilson Michael Zech Robert B Hufnagel Jesse Slone Xinjian Wang | 2022/2 |
Efficient estimation of indirect effects in case‐control studies using a unified likelihood framework | Statistics in medicine | Glen A Satten Sarah W Curtis Claudia Solis‐Lemus Elizabeth J Leslie Michael P Epstein | 2022/7/10 |
Genetic models and approaches to study orofacial clefts | Elizabeth J Leslie | 2022/7 | |
Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate | Human Genetics and Genomics Advances | Julia Welzenbach Nigel L Hammond Miloš Nikolić Frederic Thieme Nina Ishorst | 2021/7/8 |
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip | Human Genetics and Genomics Advances | Sarah W Curtis Daniel Chang Myoung Keun Lee John R Shaffer Karlijne Indencleef | 2021/4/8 |
Craniofacial features of 3q29 deletion syndrome: Application of next‐generation phenotyping technology | American Journal of Medical Genetics Part A | Bryan C Mak Rossana Sanchez Russo Michael J Gambello Nicole Fleischer Emily D Black | 2021/7 |
