Jeffrey C. Murray

Biochemistry, Genetics and Molecular BiologyMedicine

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 2%percentile

2.0Author 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.

Axenfeld-Rieger syndrome: more than meets the eye

Journal of Medical Genetics(2022)10.1136/jmg-2022-108646

Top 12%

1.7DataRank

Top 12%81 citations

Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Lubica Dudakova, Samuel Thompson +22 more

Papers

Driven by 55 papers — median percentile 30. Top paper: “Axenfeld-Rieger syndrome: more than meets the eye”.

Axenfeld-Rieger syndrome: more than meets the eye

Journal of Medical Genetics(2022)10.1136/jmg-2022-108646

Top 12%

1.7DataRank

Top 12%81 citations

Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Lubica Dudakova, Samuel Thompson +22 more

Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother–infant pairs

PLoS Medicine(2020)10.1371/journal.pmed.1003305

N/A

1.5DataRank · unranked

92 citations

Jonas Bačelis, Pol Solé-Navais, Amit Kumar Srivastava, Julius Juodakis, Amy Rouse +13 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

Multiomics Characterization of Preterm Birth in Low- and Middle-Income Countries

JAMA Network Open(2020)10.1001/jamanetworkopen.2020.29655

N/A

0.704DataRank · unranked

108 citations

Sunil Sazawal, Abdullah H Baqui, Muhammad Imran Nisar, Usha Dhingra, Rasheda Khanam +73 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

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

Scientific Reports(2022)10.1038/s41598-022-15885-1

N/A

0.553DataRank · unranked

39 citations

Peter Mossey, Jacqueline B. Hetmanski, Lord Jephthah Joojo Gowans, Mekonen Eshete, Wasiu Lanre Adeyemo +35 more

Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries

Science Advances(2023)10.1126/sciadv.ade7692

N/A

0.538DataRank · unranked

35 citations

Waqasuddin Khan, Rasheda Khanam, Sayan Das, Javairia Khalid, Jesmin Pervin +52 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

0.477DataRank · unranked

23 citations

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

Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth

Scientific Reports(2021)10.1038/s41598-021-96374-9

N/A

0.457DataRank · unranked

20 citations

Heli Tiensuu, Antti M. Haapalainen, Anu Pasanen, Pinja Tissarinen, Minna K. Karjalainen +10 more

Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort

Frontiers in Dental Medicine(2022)10.3389/fdmed.2021.771116

N/A

0.442DataRank · unranked

18 citations

Brian J. Howe, Lina M. Moreno Uribe, Consuelo Valencia Ramirez, Claudia Restrepo, Frederic W.‐B. Deleyiannis +11 more

CDH1 Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer

Genes(2020)10.3390/genes11040391

N/A

0.425DataRank · unranked

16 citations

Cheng Yee Nixon, Ying Zhu, Luigi Scietti, Federico Forneris, Lina M. Moreno Uribe +8 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

Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P)

The Cleft Palate-Craniofacial Journal(2021)10.1177/10556656211036316

N/A

0.345DataRank · unranked

9 citations

Carissa Comnick, Peter Mossey, Mekonen Eshete, Wasiu Lanre Adeyemo, Thirona Naicker +24 more

Shared genetic risk between major orofacial cleft phenotypes in an African population

Genetic Epidemiology(2024)10.1002/gepi.22564

N/A

0.327DataRank · unranked

6 citations

Tabitha Peter, Tamara Busch, Waheed Awotoye, Deepti Anand, Oladayo Abimbola +18 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

Rare variants analyses suggest novel cleft genes in the African population

Scientific Reports(2024)10.1038/s41598-024-65151-9

N/A

0.269DataRank · unranked

5 citations

Peter Mossey, Waheed Awotoye, Tamara Busch, Abimbola Oladayo, Emmanuel Aladenika +17 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

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

0.165DataRank · unranked

2 citations

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

0.117DataRank · unranked

1 citations

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

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

medRxiv(2025)10.1101/2025.01.17.25320742

N/A

0.104DataRank · unranked

1 citations

Sunil Kumar Singh, Rachel B Walkup, Dorelle V. Fawwal, Wasiu Lanre Adeyemo, Terri H. Beaty +21 more

Interrogating the causal effects of maternal circulating CRP on gestational duration and birth weight

medRxiv(2022)10.1101/2022.05.16.22275164

Top 78%

0.104DataRank

Top 78%1 citations

Pol Solé-Navais, Huan Xu, Christopher Flatley, Jonas Bačelis, Nagendra Monangi +9 more

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

Genes(2025)10.3390/genes16080876

N/A

0.104DataRank · unranked

1 citations

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

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

medRxiv(2020)10.1101/2020.11.30.20241141

N/A

0.104DataRank · unranked

1 citations

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

Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa

AJOB Empirical Bioethics(2024)10.1080/23294515.2024.2302993

N/A

0DataRank · unranked

5 citations

Sydney Prochaska, Tamara Busch, Wasiu Lanre Adeyemo, Lord Jephthah Joojo Gowans, Mekonen Eshete +9 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

Rare Variants Analyses Suggest Novel Cleft Genes in the African Population

Research Square(2024)10.21203/rs.3.rs-3921355/v1

N/A

0DataRank · unranked

0 citations

Peter Mossey, Waheed Awotoye, Tamara Busch, Abimbola Oladayo, Emmanuel Aladenika +17 more

Genetic and Epigenetic Contributors to Cleft Laterality: Evidence from Monozygotic Mirror Twins and Replication Cohorts

medRxiv(2024)10.1101/2024.11.16.24317351

N/A

0DataRank · unranked

0 citations

Waheed Awotoye, Christina E. Spencer, Ligiane A. Machado-Paula, Luke Hovey, Henry Keen +10 more

Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant Inheritance

The Cleft Palate-Craniofacial Journal(2025)10.1177/10556656241306202

N/A

0DataRank · unranked

0 citations

Ligiane A. Machado-Paula, Austin Hinkle, Luke Hovey, Waheed Awotoye, Michael S. Chimenti +10 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

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

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

Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders

genesis(2020)10.1002/dvg.23394

N/A

0DataRank · unranked

15 citations

Thomas O. Raymond, Lisa A. Lansdon, Benjamin W. Darbro, Jeffrey C. Murray, J. Robert Manak +2 more

SPECC1L regulates palate development downstream of IRF6

Human Molecular Genetics(2020)10.1093/hmg/ddaa002

N/A

0DataRank · unranked

27 citations

Luke W. Wenger, Nathan R. Wilson, Sraavya S Undurty-Akella, Jennifer Standley, Eno-Abasi Augustine-Akpan +23 more

Advancing human health in the decade ahead: pregnancy as a key window for discovery

American Journal of Obstetrics and Gynecology(2020)10.1016/j.ajog.2020.06.031

N/A

0DataRank · unranked

23 citations

Sam Mesiano, Graham J. Burton, Michelle Lampl, Jeffrey C. Murray, Rachel M. Freathy +12 more

Risk of preeclampsia in patients with genetic predisposition to common medical conditions: a case-control study

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.04.976472

N/A

0DataRank · unranked

0 citations

Vesela Kovacheva, Hooman Mirzakhani, Andrew Bjonnes, Berta Almoguera, Melissa L. Wilson +11 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

Non-Invasive Fetal Genome Sequencing: Opportunities and Challenges

(2020)10.4324/9781003074984-13

N/A

0DataRank · unranked

0 citations

Jeffrey C. Murray, Hilary S. Gammill, Jacob O. Kitzman, Matthew W. Snyder, Mario Ventura +10 more

Maternal underweight and obesity and risk of orofacial clefts in a large international consortium of population-based studies

UNC Libraries(2020)10.17615/6aq1-tj36

N/A

0DataRank · unranked

0 citations

Ronald G. Munger, Sonja A. Rasmussen, Hebah Alawi Kutbi, Paul A. Romitti, Andrew F. Olshan +8 more

A retrospective study of administration of vaccination for hepatitis B among newborn infants prior to hospital discharge at a midwestern tertiary care center

UNC Libraries(2020)10.17615/hth9-2649

N/A

0DataRank · unranked

0 citations

Cassandra N. Spracklen, Helen I. Myers, Jeffrey C. Murray, Kelli K. Ryckman

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

UNC Libraries(2020)10.17615/5188-7m66

N/A

0DataRank · unranked

0 citations

Donna M. McDonald‐McGinn, Mauricio Arcos‐Burgos, Lina M. Moreno, Andrew C. Lidral, Michel Bahuau +21 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

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

Co‐occurrence of orofacial clefts and clubfoot phenotypes in a sub‐Saharan African cohort: Whole‐exome sequencing implicates multiple syndromes and genes

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1655

N/A

0DataRank · unranked

9 citations

Noura Al Dhaheri, Mary Li, Tamara Busch, Solomon Obiri‐Yeboah, Alexander Acheampong Oti +13 more

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

Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.11.012

N/A

0DataRank · unranked

20 citations

Amanda Dickinson, Sydney Arlis, Huan Liu, Arman Hlas, Alyssa Hahn +15 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

Targeted newborn metabolomics: prediction of gestational age from cord blood

Zenodo (CERN European Organization for Nuclear Research)(2022)10.5281/zenodo.6619479

N/A

0DataRank · unranked

0 citations

Scott P. Oltman, Elizabeth E. Rogers, John M. Dagle, Jeffrey C. Murray, Moses R. Kamya +13 more

Clinically actionable secondary findings in 130 triads from sub‐Saharan African families with non‐syndromic orofacial clefts

Molecular Genetics & Genomic Medicine(2023)10.1002/mgg3.2237

N/A

0DataRank · unranked

5 citations

Lord Jephthah Joojo Gowans, Waheed Awotoye, Azeez Alade, Tamara Busch, Thirona Naicker +23 more

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63130

N/A

0DataRank · unranked

3 citations

Soumya Rao, Sandra von Hardenberg, Dong Li, Liza L. Cox, Paul C. Lee +34 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

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

Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research

BMC Public Health(2024)10.1186/s12889-024-17987-z

N/A

0DataRank · unranked

7 citations

Oluwakemi Ololade Odukoya, Veronica Sule, Ikenna Daniel Molobe, Tamara Busch, Babatunde Akodu +11 more

Jeffrey C. Murray

Indexed papers

Top data-sharing exemplar

Papers