Elizabeth J. Leslie

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 4%percentile

0.826Author DataRank

Indexed papers

5in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 5 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Gene expression patterns of the developing human face at single cell resolution reveal cell type contributions to normal facial variation and disease risk

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.18.633396

Top 48%

0.371DataRank

Top 48%8 citations

Emma Wentworth Winchester, Brian M. Schilder, Kelsey Robinson, Sarah W. Curtis, Nathan Skene +3 more

Papers

Driven by 46 papers — median percentile 44. Top paper: “Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18”.

Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18

eLife(2020)10.7554/elife.51325

N/A

1.1DataRank · unranked

45 citations

Kaylia Duncan, Annika Helverson, Priyanka Kumari, Camille Mumm, Yao Xiao +8 more

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

Genetic Epidemiology(2019)10.1002/gepi.22214

N/A

0.593DataRank · unranked

51 citations

Deepti Anand, Azeez Butali, Carmen J. Buxo, Kaare Christensen, Frederic Deleyiannis +16 more

Integrative analysis of transcriptome dynamics during human craniofacial development identifies candidate disease genes

Nature Communications(2023)10.1038/s41467-023-40363-1

N/A

0.581DataRank · unranked

47 citations

Sungryong Oh, Emma Wentworth Winchester, Andrea Wilderman, Kelsey Robinson, Tia Gordon +6 more

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100234

N/A

0.406DataRank · unranked

14 citations

Trenell J. Mosley, Kenneth S. Rivera-González, Christopher R. Jabbarpour, Sarah W. Curtis, Wasiu Lanre Adeyemo +16 more

Gene expression patterns of the developing human face at single cell resolution reveal cell type contributions to normal facial variation and disease risk

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.18.633396

Top 48%

0.371DataRank

Top 48%8 citations

Emma Wentworth Winchester, Brian M. Schilder, Kelsey Robinson, Sarah W. Curtis, Nathan Skene +3 more

Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk

Frontiers in Cell and Developmental Biology(2022)10.3389/fcell.2022.621261

N/A

0.371DataRank · unranked

9 citations

John R. Shaffer, Fred Deleyiannis, Jacqueline T. Hecht, George L. Wehby, Kaare Christensen +5 more

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

10.1101/332270

N/A

0.292DataRank · unranked

6 citations

Deepti Anand, Azeez Butali, Carmen J. Buxo, Kaare Christensen, Frederic Deleyiannis +16 more

Comprehensive phenotyping of 3q29 deletion syndrome: recommendations for clinical care

medRxiv(2020)10.1101/2020.07.25.20162149

Top 56%

0.290DataRank

Top 56%4 citations

Michael J. Gambello, Melissa M. Murphy, Katrina Aberizk, Emily Black, T. Lindsey Burrell +19 more

Identification of functional non-coding variants associated with orofacial cleft

Nature Communications(2025)10.1038/s41467-025-61734-w

N/A

0.269DataRank · unranked

5 citations

Ryan Z. Friedman, Sarah W. Curtis, Lira Pi, Kitt Paraiso, Axel Visel +12 more

Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100313

N/A

0.208DataRank · unranked

3 citations

Fangfang Yan, Andi Liu, Yulin Dai, Chihiro Iwaya, Sarah W. Curtis +7 more

Building a growing genomic repository for maternal and fetal health through the PING Consortium

Pediatric Research(2025)10.1038/s41390-024-03793-1

Top 70%

0.165DataRank

Top 70%2 citations

Shriya Singh, Blain Fasil, Allison R. Horvath, Sarah B. Mulkey, Carlos Curé +34 more

Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk

PLoS Genetics(2025)10.1371/journal.pgen.1011581

N/A

0.104DataRank · unranked

1 citations

Xinyi Zhang, Zeynep Erdogan-Yildirim, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +14 more

Feasibility of Social Media Recruitment for Orofacial Cleft Genetic Research

The Cleft Palate-Craniofacial Journal(2021)10.1177/10556656211024484

N/A

0DataRank · unranked

2 citations

Kelly E. Manning, Elizabeth J. Leslie, Grace Carlock

Efficient Estimation of Indirect Effects in Case-Control Studies Using a Unified Likelihood Framework

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.16.452552

N/A

0DataRank · unranked

1 citations

Sarah W. Curtis, Claudia Solís‐Lemus, Elizabeth J. Leslie, Michael P. Epstein, Glen A. Satten

FAT4 Identified as a Potential Modifier of Orofacial Cleft Laterality

medRxiv(2021)10.1101/2021.03.16.21253740

N/A

0DataRank · unranked

0 citations

Daniel Chang, Miranda Sun, Michael P. Epstein, Jeffrey C. Murray, Eleanor Feingold +7 more

Feasibility of Social Media Recruitment for Orofacial Cleft Genetic Research

medRxiv(2021)10.1101/2021.03.09.21253219

N/A

0DataRank · unranked

0 citations

Kelly E. Manning, Elizabeth J. Leslie, Grace Carlock

Identification of a non‐coding SNP associated with risk for non‐syndromic orofacial clefting with allele‐specific effects on IRF6 expression in vitro

The FASEB Journal(2021)10.1096/fasebj.2021.35.s1.04015

N/A

0DataRank · unranked

0 citations

Ryan Z. Friedman, Lira Pi, Annika Helverson, Sarah W. Curtis, Fabrice Darbellay +6 more

Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes

Genetic Epidemiology(2022)10.1002/gepi.22447

N/A

0DataRank · unranked

14 citations

Eleanor Feingold, Lina Moreno‐Uribe, George L. Wehby, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton +16 more

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

medRxiv(2022)10.1101/2022.08.15.22278795

N/A

0DataRank · unranked

2 citations

Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho +18 more

POIROT: A powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.28.517712

N/A

0DataRank · unranked

0 citations

Elizabeth J. Leslie, David J. Cutler, Michael P. Epstein, S. Taylor Head

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

Genetics in Medicine(2023)10.1016/j.gim.2023.100918

N/A

0DataRank · unranked

22 citations

Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho +18 more

Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63336

N/A

0DataRank · unranked

7 citations

S. C. S. Chung, S. Taylor Head, Michael P. Epstein, Jacqueline T. Hecht, George L. Wehby +5 more

POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes

Bioinformatics(2023)10.1093/bioinformatics/btad199

N/A

0DataRank · unranked

5 citations

Elizabeth J. Leslie, David J. Cutler, Michael P. Epstein, S. Taylor Head

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.018

N/A

0DataRank · unranked

97 citations

Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay +22 more

Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?

medRxiv(2023)10.1101/2023.02.01.23285340

N/A

0DataRank · unranked

1 citations

S. C. S. Chung, S. Taylor Head, Michael P. Epstein, Jacqueline T. Hecht, George L. Wehby +5 more

Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis

Communications Biology(2024)10.1038/s42003-024-06715-3

N/A

0DataRank · unranked

10 citations

Claudio Macias-Treviño, Jason W. Mitchell, Hemma Murali, Casey Tsimbal, Eileen Dalessandro +12 more

Genome-wide study of gene-by-sex interactions identifies risks for cleft palate

Human Genetics(2024)10.1007/s00439-024-02704-y

N/A

0DataRank · unranked

4 citations

Randy L. Parrish, Wasiu Lanre Adeyemo, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +13 more

Gene-by-environment interactions involving maternal exposures with orofacial cleft risk in Filipinos

medRxiv(2024)10.1101/2024.12.16.24319123

N/A

0DataRank · unranked

0 citations

Jenna C. Carlson, Nandita Mukhopadhyay, Elizabeth J. Leslie, Carmencita D. Padilla, Jeffrey C. Murray +5 more

Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.07.02.601574

N/A

0DataRank · unranked

0 citations

Claudio Macias-Treviño, Jason W. Mitchell, Hemma Murali, Casey Tsimbal, Eileen Dalessandro +12 more

Gene-by-Environment Interactions Involving Maternal Exposures with Orofacial Cleft Risk in Filipinos

Genes(2025)10.3390/genes16080876

N/A

0DataRank · unranked

1 citations

Jenna C. Carlson, Nandita Mukhopadhyay, Elizabeth J. Leslie, Carmencita D. Padilla, Jeffrey C. Murray +5 more

Functional Annotation of De Novo Variants Found Near GWAS Loci Associated With Cleft Lip With or Without Cleft Palate

Birth Defects Research(2025)10.1002/bdr2.2499

N/A

0DataRank · unranked

1 citations

Laura Cook, Kitt Paraiso, Axel Visel, Justin Cotney, Jeffrey C. Murray +5 more

Cell Cycle Arrest of a ‘Zippering’ Epithelial Cell Cluster Shapes the Face and is Disrupted in Craniofacial Disorders

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.28.667310

N/A

0DataRank · unranked

1 citations

Brandon Chacón, Laure Faure, Marco Losa, Rocío Hernández-Martínez, Kelsey Robinson +9 more

Haploinsufficiency of GRHL2 is associated with orofacial clefting in humans

Human Molecular Genetics(2025)10.1093/hmg/ddaf163

N/A

0DataRank · unranked

0 citations

Cinderella Yang, Alba Sanchis-Juan, Katherine Singleton, Terri H. Beaty, Florian Erger +16 more

Actomyosin contractility and a threshold of cadherin cell adhesion are required during tissue fusion

The Journal of Cell Biology(2025)10.1083/jcb.202503070

N/A

0DataRank · unranked

0 citations

Sarah W. Curtis, Grace C. Brewer, Elizabeth J. Leslie, Jeffrey O. Bush, Camilla Teng

Rare genetic variants in SEC24D modify orofacial cleft phenotypes

medRxiv(2023)10.1101/2023.03.24.23287714

N/A

0DataRank · unranked

4 citations

Jenna C. Carlson, Terri H. Beaty, Jeffrey C. Murray, Seth M. Weinberg, Mary L. Marazita +5 more

Embracing human genetics: a primer for developmental biologists

Development(2020)10.1242/dev.191114

N/A

0DataRank · unranked

3 citations

Elizabeth J. Leslie

The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only

medRxiv(2020)10.1101/2020.11.30.20241141

N/A

0DataRank · unranked

1 citations

Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein +10 more

Analysis of zebrafish periderm enhancers facilitates identification of a regulatory variant near human KRT8/18

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.27.921320

N/A

0DataRank · unranked

0 citations

Kaylia Duncan, Annika Helverson, Priyanka Kumari, Camille Mumm, Yao Xiao +8 more

Coding de novo mutations identified by WGS reveal novel orofacial cleft genes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.019927

N/A

0DataRank · unranked

0 citations

Kimberly Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay +22 more

Genome-wide interaction study implicates VGLL2 and alcohol exposure and PRL and smoking in orofacial cleft risk

medRxiv(2020)10.1101/2020.10.26.20219980

N/A

0DataRank · unranked

0 citations

John R. Shaffer, Fred Deleyiannis, Jacqueline T. Hecht, George L. Wehby, Kaare Christensen +5 more

Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios

PLoS Genetics(2021)10.1371/journal.pgen.1009584

N/A

0DataRank · unranked

53 citations

Sowmya Venkataraghavan, Wanying Zhang, Elizabeth J. Leslie, Jacqueline B. Hetmanski, Seth M. Weinberg +6 more

Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.621482

N/A

0DataRank · unranked

33 citations

Eleanor Feingold, Lina Moreno‐Uribe, George L. Wehby, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton +16 more

Genetic models and approaches to study orofacial clefts

Oral Diseases(2021)10.1111/odi.14109

N/A

0DataRank · unranked

27 citations

Elizabeth J. Leslie

The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100025

N/A

0DataRank · unranked

24 citations

Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein +10 more

A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic Paraplegia

Movement Disorders(2021)10.1002/mds.28821

N/A

0DataRank · unranked

22 citations

Michael Zech, Robert B. Hufnagel, Jesse Slone, Xinjian Wang, Shelli M. Homan +13 more

Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome

Translational Psychiatry(2021)10.1038/s41398-021-01435-2

N/A

0DataRank · unranked

18 citations

Ryan H. Purcell, the Emory 3q29 Project, Katrina Aberizk, Hallie Averbach, Emily Black +37 more

Elizabeth J. Leslie

Indexed papers

Top data-sharing exemplar

Papers