Sarah W. Curtis

Biochemistry, Genetics and Molecular BiologyEnvironmental Science

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 5%percentile

0.371Author DataRank

Indexed papers

1in 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 1 indexed paper 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 22 papers — median percentile 52. Top paper: “Gene expression patterns of the developing human face at single cell resolution reveal cell type contributions to normal facial variation and disease risk”.

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

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

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

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

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

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

EBioMedicine(2022)10.1016/j.ebiom.2022.104079

N/A

0DataRank · unranked

41 citations

Colin A. Ellis, Ingrid E Scheffer, Shiva Ganesan, Costin Leu, Lynette G. Sadleir +12 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

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

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

0DataRank · unranked

14 citations

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

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

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

EBioMedicine(2024)10.1016/j.ebiom.2024.105404

N/A

0DataRank · unranked

30 citations

Ingrid E Scheffer, Colin A. Ellis, Bronwyn E. Grinton, Zaid Afawi, Dina Amrom +43 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

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

0DataRank · unranked

3 citations

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

Identification of functional non-coding variants associated with orofacial cleft

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

N/A

0DataRank · unranked

5 citations

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

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.009

N/A

0DataRank · unranked

3 citations

Sarah W. Curtis, Justin Paschall, Wasiu Lanre Adeyemo, Terri H. Beaty, Azeez Butali +14 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

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 trios

medRxiv(2025)10.1101/2025.03.03.25323233

N/A

0DataRank · unranked

0 citations

Sarah W. Curtis, Justin Paschall, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +12 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

Genome-wide DNA methylation differences and polychlorinated biphenyl (PCB) exposure in a US population

Epigenetics(2020)10.1080/15592294.2020.1795605

N/A

0DataRank · unranked

23 citations

Dawayland O. Cobb, Varun Kilaru, Metrecia L. Terrell, M. Elizabeth Marder, Dana Boyd Barr +5 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

Sarah W. Curtis

Indexed papers

Top data-sharing exemplar

Papers