Jeffrey C. Murray

1.2k total citations
21 papers, 461 citations indexed

About

Jeffrey C. Murray is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jeffrey C. Murray has authored 21 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jeffrey C. Murray's work include Cleft Lip and Palate Research (9 papers), Craniofacial Disorders and Treatments (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jeffrey C. Murray is often cited by papers focused on Cleft Lip and Palate Research (9 papers), Craniofacial Disorders and Treatments (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jeffrey C. Murray collaborates with scholars based in United States, Brazil and Ghana. Jeffrey C. Murray's co-authors include Aline Petrin, Nancy J. Leysens, Koh-ichiro Yoshiura, David Merrill, Antônio Richieri‐Costa, Roger A. Williamson, Janet I. Andrews, Rebecca S. Reiter, Natalia Freitas Rossi and Dagma Venturini Marques Abramides and has published in prestigious journals such as Cancer Research, Diabetes and Genetics.

In The Last Decade

Jeffrey C. Murray

21 papers receiving 451 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jeffrey C. Murray United States 14 231 209 71 60 43 21 461
Marie‐Pierre Cordier France 11 189 0.8× 168 0.8× 18 0.3× 119 2.0× 82 1.9× 34 438
F. George Otieno United States 12 628 2.7× 307 1.5× 15 0.2× 69 1.1× 87 2.0× 14 966
Omar Abidi Morocco 14 137 0.6× 215 1.0× 18 0.3× 22 0.4× 20 0.5× 36 473
Stavit Shalev Israel 14 70 0.3× 172 0.8× 17 0.2× 111 1.9× 92 2.1× 29 536
LaDonna Immken United States 13 339 1.5× 372 1.8× 14 0.2× 112 1.9× 79 1.8× 21 689
A. David France 13 230 1.0× 326 1.6× 18 0.3× 64 1.1× 115 2.7× 42 579
Silvia Maitz Italy 17 319 1.4× 330 1.6× 43 0.6× 123 2.0× 65 1.5× 40 617
Chia‐Cheng Hung Taiwan 19 181 0.8× 310 1.5× 14 0.2× 146 2.4× 81 1.9× 38 785
Filomena Tiziana Papa Italy 14 257 1.1× 182 0.9× 15 0.2× 41 0.7× 14 0.3× 26 412
Yingjun Xie China 13 157 0.7× 279 1.3× 10 0.1× 138 2.3× 63 1.5× 65 543

Countries citing papers authored by Jeffrey C. Murray

Since Specialization
Citations

This map shows the geographic impact of Jeffrey C. Murray's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jeffrey C. Murray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jeffrey C. Murray more than expected).

Fields of papers citing papers by Jeffrey C. Murray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey C. Murray. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jeffrey C. Murray. The network helps show where Jeffrey C. Murray may publish in the future.

Co-authorship network of co-authors of Jeffrey C. Murray

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey C. Murray. A scholar is included among the top collaborators of Jeffrey C. Murray based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jeffrey C. Murray. Jeffrey C. Murray is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Odukoya, Oluwakemi Ololade, Tamara Busch, Wasiu Lanre Adeyemo, et al.. (2024). Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research. BMC Public Health. 24(1). 507–507. 3 indexed citations
2.
Busch, Tamara, Wasiu Lanre Adeyemo, Lord Jephthah Joojo Gowans, et al.. (2024). Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa. AJOB Empirical Bioethics. 15(2). 133–146. 1 indexed citations
3.
Gowans, Lord Jephthah Joojo, Mary Li, Tamara Busch, et al.. (2021). 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. 9(4). e1655–e1655. 4 indexed citations
4.
Sankpal, Umesh T., W. Paul Bowman, Jeffrey C. Murray, & Riyaz Basha. (2017). Abstract 12: Evaluation of metformin and clotam combination for medulloblastoma. Cancer Research. 77(13_Supplement). 12–12. 1 indexed citations
5.
Liu, Huan, Tamara Busch, Steven Eliason, et al.. (2016). Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate. Birth Defects Research. 109(1). 27–37. 33 indexed citations
6.
Stodgell, Chris, Richard K. Miller, Jeffrey C. Murray, et al.. (2014). Lack of correlation between placental gene expression and RNA integrity number (RIN) or time to collection. Placenta. 35(9). A46–A47. 4 indexed citations
7.
Kokitsu‐Nakata, Nancy Mizue, Aline Petrin, Jason Heard, et al.. (2012). Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome. American Journal of Medical Genetics Part A. 158A(8). 2003–2008. 13 indexed citations
8.
Saadi, Irfan, Fowzan S. Alkuraya, Stephen S. Gisselbrecht, et al.. (2011). Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting. The American Journal of Human Genetics. 89(1). 44–55. 55 indexed citations
9.
Jobling, Rebekah, et al.. (2011). Monozygotic twins with variable expression of Van der Woude Syndrome. American Journal of Medical Genetics Part A. 155(8). 2008–2010. 9 indexed citations
10.
Félix, Têmis Maria, Aline Petrin, Maria Teresa Vieira Sanseverino, & Jeffrey C. Murray. (2010). Further characterization of microdeletion syndrome involving 2p15‐p16.1. American Journal of Medical Genetics Part A. 152A(10). 2604–2608. 25 indexed citations
11.
Petrin, Aline, Célia Maria Giacheti, Luciana Paula Maximino, et al.. (2010). Identification of a microdeletion at the 7q33‐q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. American Journal of Medical Genetics Part A. 152A(12). 3164–3172. 51 indexed citations
12.
Petrin, Aline, Sandra Daack‐Hirsch, Jamie L’Heureux, & Jeffrey C. Murray. (2010). A Case of 3q29 Microdeletion Syndrome Involving Oral Cleft Inherited from a Nonaffected Mosaic Parent: Molecular Analysis and Ethical Implications. The Cleft Palate-Craniofacial Journal. 48(2). 222–230. 8 indexed citations
13.
14.
Dobbs, Matthew B., Frederick R. Dietz, Christina A. Gurnett, et al.. (2000). Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36. Journal of Orthopaedic Research®. 18(3). 340–344. 15 indexed citations
15.
Yoshiura, Koh-ichiro, Nancy J. Leysens, Rebecca S. Reiter, & Jeffrey C. Murray. (1998). Cloning, Characterization, and Mapping of the Mouse Homeobox GeneHmx1. Genomics. 50(1). 61–68. 36 indexed citations
16.
Yoshiura, Koh-ichiro, et al.. (1997). Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes. American Journal of Medical Genetics. 72(3). 354–362. 17 indexed citations
17.
Sunden, Sara L.F., John S. Beck, Julie M. Gastier, et al.. (1996). Chromosomal Assignment of 2900 Tri- and Tetranucleotide Repeat Markers Using NIGMS Somatic Cell Hybrid Panel 2. Genomics. 32(1). 15–20. 19 indexed citations
18.
Murray, Jeffrey C.. (1994). Using Granulocyte Colony-Stimulating Factor for Neutropenia During Neonatal Sepsis. Archives of Pediatrics and Adolescent Medicine. 148(7). 764–764. 14 indexed citations
19.
Mathews, Katherine D., Holly H Ardinger, Darryl Nishimura, et al.. (1989). Linkage localization of Börjeson‐Forssman‐Lehmann syndrome. American Journal of Medical Genetics. 34(4). 470–474. 28 indexed citations
20.
Bell, Graeme I., Jeffrey C. Murray, Yusuke Nakamura, et al.. (1989). Polymorphic Human Insulin-Responsive Glucose-Transporter Gene on Chromosome 17p13. Diabetes. 38(8). 1072–1075. 28 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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