Jeff Murray

508 total citations
8 papers, 100 citations indexed

About

Jeff Murray is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Genetics. According to data from OpenAlex, Jeff Murray has authored 8 papers receiving a total of 100 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Radiology, Nuclear Medicine and Imaging and 2 papers in Genetics. Recurrent topics in Jeff Murray's work include Cleft Lip and Palate Research (2 papers), Neonatal and fetal brain pathology (1 paper) and Craniofacial Disorders and Treatments (1 paper). Jeff Murray is often cited by papers focused on Cleft Lip and Palate Research (2 papers), Neonatal and fetal brain pathology (1 paper) and Craniofacial Disorders and Treatments (1 paper). Jeff Murray collaborates with scholars based in United States, Sweden and Italy. Jeff Murray's co-authors include Jørn Olsen, Anders Ekbom, Kaare Christensen, Terri L. Young, Tarah T. Colaizy, Margaret M. DeAngelis, C. Michael Cotten, John M. Dagle, Allison M. Momany and Grier P. Page and has published in prestigious journals such as Investigative Ophthalmology & Visual Science, Journal of the Neurological Sciences and American Journal of Medical Genetics.

In The Last Decade

Jeff Murray

8 papers receiving 100 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jeff Murray United States	6	34	31	27	17	15	8	100
Barbara Mikat Germany	7	12 0.4×	15 0.5×	42 1.6×	27 1.6×	8 0.5×	7	127
Antoinette Schouten‐van Meeteren Netherlands	5	14 0.4×	14 0.5×	56 2.1×	40 2.4×	3 0.2×	5	161
Jill Beis Canada	3	31 0.9×	20 0.6×	12 0.4×	24 1.4×		4	62
Vasumathy Vedantham India	9	56 1.6×	20 0.6×	4 0.1×	34 2.0×	5 0.3×	17	178
Hongzhen Li China	8	4 0.1×	18 0.6×	16 0.6×	21 1.2×	8 0.5×	16	120
Vasudha Kemmanu India	11	119 3.5×	22 0.7×	27 1.0×	25 1.5×	4 0.3×	22	245
Forest Riekhof United States	5	62 1.8×	11 0.4×	24 0.9×	20 1.2×	2 0.1×	16	138
Tanuja Vaidya India	6	94 2.8×	27 0.9×	8 0.3×	21 1.2×	1 0.1×	16	191
Cheryl Fischer United States	7	32 0.9×	13 0.4×	23 0.9×	14 0.8×		10	113
Ting Yin China	9	88 2.6×	10 0.3×	58 2.1×	13 0.8×	1 0.1×	38	194

Countries citing papers authored by Jeff Murray

Since Specialization

Citations

This map shows the geographic impact of Jeff 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 Jeff Murray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jeff Murray more than expected).

Fields of papers citing papers by Jeff Murray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeff Murray

This figure shows the co-authorship network connecting the top 25 collaborators of Jeff Murray. A scholar is included among the top collaborators of Jeff 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 Jeff Murray. Jeff Murray is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Qian, Fang, et al.. (2024). DNA Methylation Effects on Van der Woude Syndrome Phenotypic Variability. The Cleft Palate-Craniofacial Journal. 62(10). 1641–1650. 1 indexed citations

2.

Tracy, LaRee, et al.. (2017). US FDA Perspective on Elbasvir/Grazoprevir Treatment for Patients with Chronic Hepatitis C Virus Genotype 1 or 4 Infection. Clinical Drug Investigation. 37(4). 317–326. 9 indexed citations

3.

VanderMeer, Julia E., Tonia C. Carter, Faith Pangilinan, et al.. (2016). Evaluation of proton‐coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. American Journal of Medical Genetics Part A. 170(4). 1007–1016. 5 indexed citations

4.

Hartnett, M. Elizabeth, Margaux A. Morrison, Tammy L. Yanovitch, et al.. (2014). Genetic Variants Associated With Severe Retinopathy of Prematurity in Extremely Low Birth Weight Infants. Investigative Ophthalmology & Visual Science. 55(10). 6194–6194. 40 indexed citations

5.

Olsen, Jørn, Kaare Christensen, Jeff Murray, & Anders Ekbom. (2010). An Introduction to Epidemiology for Health Professionals. DIAL (Catholic University of Leuven). 20 indexed citations

6.

Murray, Jeff. (2007). Unaccompanied Minors in an Academic Library. 28(3). 10. 1 indexed citations

7.

Siniscalco, M., I. Oberlé, Paola Melis, et al.. (1991). Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site. American Journal of Medical Genetics. 38(2-3). 357–362. 14 indexed citations

8.

Ionâşescu, Victor, Jeff Murray, Trudy L. Burns, et al.. (1987). Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I). Journal of the Neurological Sciences. 80(1). 73–78. 10 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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