Edward R.B. McCabe

14.6k citations

252 papers · 10.4k indexed · 3 hit papers · h-index 52

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Genetics top 0.2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases

Papers in

Clinical Biochemistry 54
- Metabolism and Genetic Disorders 53
Genetics 77
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 26
- Genomics and Rare Diseases 22

Co-authors: Katrina M. Dipple Linda L. McCabe Thomas P. Burris Bruce D. Gelb Weiwen Guo Soojung Hur Dino Di Carlo Anita K. Iyer
Journals: Molecular Genetics and Metabolism (42 papers)Pediatric Research (18 papers)The Journal of Pediatrics (12 papers)PEDIATRICS (10 papers)Genetics in Medicine (6 papers)
Partner nations: United States Italy Germany

In The Last Decade

Edward R.B. McCabe

245 papers receiving 10.1k citations

Hit Papers

align trajectories log scale

Enabling Technologies for Personalized and Precision Medicine 2020 · 264 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2020 Trends in biotechnology
2011 Lab on a Chip
1994 Nature

Peers

Replace Thomas J. Hudson with:

Thomas J. Hudson Canada

Aarno Palotie Finland

Bruno Dallapiccola Italy

Christine N. Metz United States

Peter K. Gregersen United States

Robert P. Erickson United States

Giuseppe Novelli Italy

Peter Nürnberg Germany

Henry H. Heng United States

Walter Malorni Italy

Edward R.B. McCabe relative to Thomas J. Hudson Canada Thomas J. Hudson's profile →

Citations per field

00.5×2×3×4.0×

Thomas J. Hudson · 1×

×4.0 2k/376

CB

×0.6 3k/6k

GENET

×0.6 6k/10k

MB

×2.6 623/236

RM

×0.7 814/1k

EDM

Citations per year

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Countries citing papers authored by Edward R.B. McCabe

Since Specialization

Citations

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

Fields of papers citing papers by Edward R.B. McCabe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward R.B. McCabe. 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 Edward R.B. McCabe. The network helps show where Edward R.B. McCabe may publish in the future.

Co-authors

The 25 scholars most cited alongside Edward R.B. McCabe, 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 Edward R.B. McCabe Line = papers co-authored together Edward R.B. McCabe links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Deformability-based cell classification and enrichment using inertial microfluidics Lab on a Chip ·Soojung Hur, Nicole K. Henderson-MacLennan, Edward R.B. McCabe, Dino Di Carlo Hit paper breakdown →	2011	459
2	2009 Presidential Address: Beyond Darwin? Evolution, Coevolution, and the American Society of Human Genetics The American Journal of Human Genetics ·Edward R.B. McCabe	2010	0
3	ff1b, the SF1 ortholog, is important for pancreatic islet cell development in zebrafish Molecular Genetics and Metabolism ·Jaime K. Mazilu, Jamie W. Powers, Shuo Lin, Edward R.B. McCabe	2010	3
4	Nanopediatrics: Enabling Personalized Medicine for Children Pediatric Research ·Edward R.B. McCabe	2010	9
5	EWS/FLI and Its Downstream Target NR0B1 Interact Directly to Modulate Transcription and Oncogenesis in Ewing's Sarcoma Cancer Research ·Michelle Kinsey, Richard A. Smith, Anita K. Iyer, Edward R.B. McCabe, Stephen L. Lessnick	2009	74
6	Novel role for the orphan nuclear receptor Dax1 in embryogenesis, different from steroidogenesis Molecular Genetics and Metabolism ·Kathy K. Niakan, Emily C. Davis, Robert C. Clipsham, Meisheng Jiang, Deborah B. Dehart, Kathleen K. Sulik, Edward R.B. McCabe	2006	84
7	IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric ofDAX1 Human Mutation ·Yao‐Hua Zhang, Bing-Ling Huang, Kathy K. Niakan, Linda L. McCabe, Edward R.B. McCabe, Katrina M. Dipple	2004	34
8	Translational genomics in medical genetics Genetics in Medicine ·Edward R.B. McCabe	2002	5
9	AluY insertion (IVS4-52ins316alu) in the glycerol kinase gene from an individual with benign glycerol kinase deficiency Human Mutation ·Y.-H. Zhang, Katrina M. Dipple, Éric Vilain, Binquan Huang, G. Finlayson, Bradford L. Therrell, Kim C. Worley, Prescott L. Deininger, Edward R.B. McCabe	2000	33
10	IMAGe, a New Clinical Association of Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies The Journal of Clinical Endocrinology & Metabolism ·Éric Vilain, Martine Le Merrer, C Lecointre, F Desangles, Mark A. Kay, P Maroteaux, Edward R.B. McCabe	1999	78
11	Mammalian Sex Determination: From Gonads to Brain Molecular Genetics and Metabolism ·Éric Vilain, Edward R.B. McCabe	1998	67
12	Identification of a Ferritin Light Chain Pseudogene Near the Glycerol Kinase Locus in Xp21 by cDNA Amplification for Identification of Genomic Expressed Sequences Biochemical and Molecular Medicine ·Weiwen Guo, Volker Adams, Jestina Mason, Edward R.B. McCabe	1997	1
13	Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene Nature Genetics ·Weiwen Guo, Kim C. Worley, Volker Adams, Jestina Mason, Desirée Sylvester-Jackson, Yaohua Zhang, Jeffrey A. Towbin, Donna D. Fogt, Stella Madu, David A. Wheeler, Edward R.B. McCabe	1993	37
14	Developmental expression of hexokinase 1 in the rat Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Lisa Griffin, Bruce D. Gelb, Volker Adams, Edward R.B. McCabe	1992	30
15	Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia. Journal of Clinical Investigation ·Edward R.B. McCabe, Jeffrey A. Towbin, Jeffrey S. Chamberlain, L. Baumbach, Jan Witkowski, G J van Ommen, M. Kœnig, Louis M. Kunkel, William Seltzer	1989	48
16	Muscle glycerol kinase in Duchenne dystrophy and glycerol kinase deficiency Muscle & Nerve ·William Seltzer, C. Angelini, Gulshan Dhariwal, Steven P. Ringel, Edward R.B. McCabe	1989	16
17	Multiple Acyl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type II) with Transient Hypersarcosinemia and Sarcosinuria; Possible Inherited Deficiency of an Electron Transfer Flavoprotein Pediatric Research ·Stephen I. Goodman, Edward R.B. McCabe, Paul V. Fennessey, John Mace	1980	77
18	Multiple Acyl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type II) with Transient Hypersarcosinemia and Sarcosinuria; Possible Inherited Deficiency of an Electron Transfer Flavoprotein Pediatric Research ·Stephen I. Goodman, Edward R.B. McCabe, Paul V. Fennessey, John Mace	1980	7
19	Zinc absorption and low phenylalanine diets. Pediatric Research ·ClareE. Casey, Arlene Ernest, K. Michael Hambidge, Edward R.B. McCabe, P A Walravens	1980	1
20	Alcoholism: The hidden alcoholic in the African polyclinic SHILAP Revista de lepidopterología ·Edward R.B. McCabe	1980	1

About Edward R.B. McCabe

Edward R.B. McCabe is a scholar working on Clinical Biochemistry, Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics, having authored 252 papers that have together received 10.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (53 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (26 papers), Mitochondrial Function and Pathology (22 papers), Genomics and Rare Diseases (22 papers), Sexual Differentiation and Disorders (20 papers), Cancer, Hypoxia, and Metabolism (19 papers), RNA modifications and cancer (18 papers) and Metabolism, Diabetes, and Cancer (18 papers). The work is most often cited by research in Clinical Biochemistry (1.5k citations), Genetics (3.3k citations), Molecular Biology (5.5k citations), Reproductive Medicine (623 citations) and Endocrinology, Diabetes and Metabolism (814 citations). Edward R.B. McCabe has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Katrina M. Dipple, Linda L. McCabe, Thomas P. Burris, Bruce D. Gelb, Weiwen Guo, Soojung Hur, Dino Di Carlo, Anita K. Iyer, Jeffrey A. Towbin and William Seltzer. Their work appears in journals such as Molecular Genetics and Metabolism, Pediatric Research, The Journal of Pediatrics, PEDIATRICS and Genetics in Medicine.

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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