J.C. Murray

2.5k citations

24 papers · 1.9k indexed · 1 hit paper · h-index 17

Impact in

Genetics top 2%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
Developmental Biology top 5%

Papers in ⓘ

Genetics 11
- Cleft Lip and Palate Research 4
- Congenital Ear and Nasal Anomalies 3
- Craniofacial Disorders and Treatments 3
Molecular Biology 10
- Angiogenesis and VEGF in Cancer 4
- dental development and anomalies 2

Co-authors: Peter W. Hewett (4 shared papers)Elena V. Semina (2 shared papers)Nicole A. Datson (1 shared paper)Wallace L.M. Alward (1 shared paper)Kent W. Small (1 shared paper)Pierre Bitoun (1 shared paper)John C. Carey (1 shared paper)Bernhard Zabel (1 shared paper)
Journals: Human Molecular Genetics (2 papers)In Vitro Cellular & Developmental Biology - Animal (2 papers)British Journal of Dermatology (2 papers)Genomics (2 papers)Advanced Drug Delivery Reviews (2 papers)
Partner nations: United States United Kingdom Japan

In The Last Decade

J.C. Murray

23 papers receiving 1.8k citations

Hit Papers

align trajectories log scale

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome 1996 · 720 citations

Peers

Countries citing papers authored by J.C. Murray

Since Specialization

Citations

This map shows the geographic impact of J.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 J.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 J.C. Murray more than expected).

Fields of papers citing papers by J.C. Murray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.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 J.C. Murray. The network helps show where J.C. Murray may publish in the future.

Co-authors

The 25 scholars most cited alongside J.C. Murray, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J.C. Murray Line = papers co-authored together J.C. Murray links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome Nature Genetics ·Elena V. Semina, Rebecca S. Reiter, Nancy J. Leysens, Wallace L.M. Alward, Kent W. Small, Nicole A. Datson, Jacqueline Siegel‐Bartelt, Diane Bierke-Nelson, Pierre Bitoun, Bernhard Zabel, John C. Carey, J.C. Murray Hit paper breakdown →	1996	720
2	Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants. PubMed ·Gary M. Shaw, Cathy R. Wasserman, Edward J. Lammer, C. D. O’Malley, J.C. Murray, Ann M. Basart, M Tolarová	1996	242
3	Isolation of a New Homeobox Gene Belonging to the Pitx/Rieg Family: Expression During Lens Development and Mapping to the Aphakia Region on Mouse Chromosome 19 Human Molecular Genetics ·Е. В. Семина, Robert S. Reiter, J.C. Murray	1997	163
4	Maternal alcohol use and risk of orofacial cleft birth defects Teratology ·Ronald G. Munger, Paul A. Romitti, Sandra Daack‐Hirsch, Trudy L. Burns, J.C. Murray, James W. Hanson	1996	108
5	Human microvessel endothelial cells: Isolation, culture and characterization In Vitro Cellular & Developmental Biology - Animal ·Peter W. Hewett, J.C. Murray	1993	81
6	Immunomagnetic purification of human microvessel endothelial cells using Dynabeads coated with monoclonal antibodies to PECAM-1. PubMed ·Peter W. Hewett, J.C. Murray	1993	65
7	Isolation and characterization of microvessel endothelial cells from human mammary adipose tissue In Vitro Cellular & Developmental Biology - Animal ·Peter W. Hewett, J.C. Murray, Elizabeth Price, M.E. Watts, M. Woodcock	1993	61
8	A single-gene explanation for the probability of having idiopathic talipes equinovarus. PubMed ·Timothy R. Rebbeck, F R Dietz, J.C. Murray, Kenneth H. Buetow	1993	60
9	Human Lung Microvessel Endothelial Cells: Isolation, Culture, and Characterization Microvascular Research ·Peter W. Hewett, J.C. Murray	1993	59
10	Characterization of a Novel Gene Disrupted by a Balanced Chromosomal Translocation t(2;19)(q11.2;q13.3) in a Family with Cleft Lip and Palate Genomics ·Koh-ichiro Yoshiura, Junichiro Machida, Sandra Daack‐Hirsch, Shivanand R. Patil, Linda K. Ashworth, Jaqueline T. Hecht, J.C. Murray	1998	57
11	Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery Journal of Perinatology ·K M Steffen, M.E. Cooper, Min Shi, Diana Caprau, HN Simhan, John M. Dagle, M.L. Marazita, J.C. Murray	2007	50
12	Characterization of the human HOX 7 cDNA and identification of polymorphic markers Human Molecular Genetics ·Babu J. Padanilam, H. Scott Stadler, K. Mills, Lillian B. Mcleod, Michael Solursh, B. Lee, Francesco Ramirez, Kenneth H. Buetow, J.C. Murray	1992	44
13	Development of a Screening Set for New (CAG/CTG)nDynamic Mutations Genomics ·Julie M. Gastier, Thomas Brody, Jacqueline C. Pulido, Thomas Businga, Sara L.F. Sunden, Xintong Hu, Shanak Maitra, K.H. Buetow, J.C. Murray, Val C. Sheffield, Mark S. Boguski, Geoffrey M. Duyk, Thomas J. Hudson	1996	35
14	Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes Clinical Genetics ·Eric Weh, Linda M. Reis, Rebecca C. Tyler, David Bick, William J. Rhead, Stephanie E Wallace, Tracy L. McGregor, Shelley K. Dills, Mei Chao, J.C. Murray, Elena V. Semina	2013	33
15	Targeting solid tumours: challenges, disappointments, and opportunities Advanced Drug Delivery Reviews ·J.C. Murray, J Carmichael	1995	22
16	Platelet-derived endothelial cell growth factor expression and angiogenesis in cervical intraepithelial neoplasia and squamous cell carcinoma of the cervix Annals of Diagnostic Pathology ·Stephen Dobbs, Laurence Brown, David Ireland, Keith R. Abrams, J.C. Murray, Keith Gatter, Adrian L. Harris, William P. Steward, Kenneth J. O’Byrne	2000	16
17	Gene-transfer systems for human endothelial cells Advanced Drug Delivery Reviews ·Stewart G. Martin, J.C. Murray	2000	16
18	The scleroatrophic syndrome of Huriez British Journal of Dermatology ·G.M. Kavanagh, Paul Da Silva Jardine, R. D. G. Peachey, J.C. Murray, D. de Berker	1997	12
19	Bacterial expression of full-length and truncated forms of cytokine EMAP-2 and cytokine-like domain of mammalian tyrosyl-tRNA synthetase Biopolymers and Cell ·Alberto Dubrovsky, J. O. Brown, A. I. Kornelyuk, J.C. Murray, G. Kh. Matsuka	2000	9
20	Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers. PubMed ·Smita Kittur, M M Bagdon, M L Lubs, John A. Phillips, J.C. Murray, Susan Slaugenhaupt, Aravinda Chakravarti, William Adler	1989	8

About J.C. Murray

J.C. Murray is a scholar working on Genetics, Molecular Biology, Cancer Research, Obstetrics and Gynecology and Genetics, having authored 24 papers that have together received 1.9k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (4 papers), Angiogenesis and VEGF in Cancer (4 papers), Congenital Ear and Nasal Anomalies (3 papers), Craniofacial Disorders and Treatments (3 papers), Protease and Inhibitor Mechanisms (3 papers), Cell Adhesion Molecules Research (2 papers), Pregnancy and preeclampsia studies (2 papers) and dental development and anomalies (2 papers). The work is most often cited by research in Genetics (747 citations), Developmental Biology (41 citations), Molecular Biology (1.1k citations), Ophthalmology (134 citations) and Immunology and Allergy (73 citations). J.C. Murray has collaborated with scholars based in United States, United Kingdom and Japan. Frequent co-authors include Peter W. Hewett, Elena V. Semina, Nicole A. Datson, Wallace L.M. Alward, Kent W. Small, Pierre Bitoun, John C. Carey, Bernhard Zabel, Jacqueline Siegel‐Bartelt and Nancy J. Leysens. Their work appears in journals such as Human Molecular Genetics, In Vitro Cellular & Developmental Biology - Animal, British Journal of Dermatology, Genomics and Advanced Drug Delivery Reviews.

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.

Explore authors with similar magnitude of impact