Steve J. Funderburk

1.4k total citations
40 papers, 1.1k citations indexed

About

Steve J. Funderburk is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Steve J. Funderburk has authored 40 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Steve J. Funderburk's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Chromosomal and Genetic Variations (6 papers). Steve J. Funderburk is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Chromosomal and Genetic Variations (6 papers). Steve J. Funderburk collaborates with scholars based in United States. Steve J. Funderburk's co-authors include R S Sparkes, Robert S. Sparkes, M. Anne Spence, L. Leigh Field, Maryellen C. Sparkes, A. Linn Murphree, Robert W. Lingua, William F. Benedict, David R. Meldrum and Barbara F. Crandall and has published in prestigious journals such as Science, New England Journal of Medicine and Journal of Biological Chemistry.

In The Last Decade

Steve J. Funderburk

40 papers receiving 956 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steve J. Funderburk United States 17 392 358 177 164 156 40 1.1k
W E Nance United States 21 323 0.8× 613 1.7× 163 0.9× 96 0.6× 107 0.7× 48 1.4k
F. A. Beemer Netherlands 28 637 1.6× 1.0k 2.9× 301 1.7× 149 0.9× 81 0.5× 73 2.0k
Tim Donlon United States 18 672 1.7× 607 1.7× 254 1.4× 139 0.8× 31 0.2× 26 1.3k
Rena E. Falk United States 19 447 1.1× 408 1.1× 174 1.0× 61 0.4× 42 0.3× 39 1.0k
Helen Kingston United Kingdom 24 645 1.6× 839 2.3× 161 0.9× 105 0.6× 45 0.3× 63 1.9k
Alan Johnston United Kingdom 18 297 0.8× 266 0.7× 52 0.3× 29 0.2× 74 0.5× 80 1.1k
M. H. K. Shokeir Canada 19 355 0.9× 557 1.6× 178 1.0× 153 0.9× 16 0.1× 48 1.3k
Mehmet Alikaşifoğlu Türkiye 21 485 1.2× 602 1.7× 126 0.7× 95 0.6× 46 0.3× 115 1.5k
K Méhes Hungary 17 717 1.8× 828 2.3× 408 2.3× 159 1.0× 18 0.1× 105 1.7k
Allan J. Ebbin United States 15 312 0.8× 185 0.5× 229 1.3× 49 0.3× 51 0.3× 32 707

Countries citing papers authored by Steve J. Funderburk

Since Specialization
Citations

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

Fields of papers citing papers by Steve J. Funderburk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steve J. Funderburk

This figure shows the co-authorship network connecting the top 25 collaborators of Steve J. Funderburk. A scholar is included among the top collaborators of Steve J. Funderburk 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 Steve J. Funderburk. Steve J. Funderburk 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.
Funderburk, Steve J., et al.. (1987). Primate evolution of a dispersed human repetitive DNA sequence. Chromosoma. 95(2). 148–153. 2 indexed citations
2.
Spence, M. Anne, Dilys M. Parry, Mary L. Marazita, et al.. (1986). Genetic Linkage Analysis of Neurofibromatosisa. Annals of the New York Academy of Sciences. 486(1). 287–292. 6 indexed citations
3.
Funderburk, Steve J., et al.. (1983). Chromosomal variants and abnormalities in couples with repeated spontaneous pregnancy loss. Pathology. 15(1). 109–109. 5 indexed citations
4.
Funderburk, Steve J., et al.. (1983). Parental reproductive problems and gestational hormonal exposure in autistic and schizophrenic children. Journal of Autism and Developmental Disorders. 13(3). 325–332. 41 indexed citations
5.
Spence, M. Anne, Dilys M. Parry, L. Leigh Field, et al.. (1983). Linkage analysis of neurofibromatosis (von Recklinghausen disease).. Journal of Medical Genetics. 20(5). 334–337. 30 indexed citations
6.
Funderburk, Steve J., et al.. (1981). Pentasomy X: Report of patient and studies of X‐inactivation. American Journal of Medical Genetics. 8(1). 27–33. 7 indexed citations
7.
Funderburk, Steve J., D. Guthrie, & David R. Meldrum. (1980). OUTCOME OF PREGNANCIES COMPLICATED BY EARLY VAGINAL BLEEDING. BJOG An International Journal of Obstetrics & Gynaecology. 87(2). 100–105. 61 indexed citations
8.
Funderburk, Steve J., R S Sparkes, & I Klisak. (1979). The 9p-syndrome.. Journal of Medical Genetics. 16(1). 75–79. 18 indexed citations
9.
10.
Mohandas, T., et al.. (1979). Regional localization of human gene loci on chromosome 9: studies of somatic cell hybrids containing human translocations.. PubMed. 31(5). 586–600. 52 indexed citations
11.
Rogawski, Michael A., Steve J. Funderburk, & Stephen D. Cederbaum. (1978). Oculocutaneous Albinism and Mental Disorder. Human Heredity. 28(2). 81–85. 17 indexed citations
12.
Funderburk, Steve J., et al.. (1978). Minor chromosome variants in child psychiatric patients. American Journal of Medical Genetics. 1(3). 301–308. 8 indexed citations
13.
Funderburk, Steve J., Ray Stewart, & John M. Opitz. (1978). The G and BBB syndromes: Case presentations, genetics, and nosology. American Journal of Medical Genetics. 2(2). 131–144. 36 indexed citations
14.
Funderburk, Steve J., Robert S. Sparkes, & Ivana Klisak. (1977). 18p- Syndrome resulting from 14q/18q ?dicentric? fusion translocation. Human Genetics. 39(2). 243–250. 16 indexed citations
15.
Funderburk, Steve J.. (1976). Acne in retarded boy with autosomal chromosomal abnormality. Archives of Dermatology. 112(6). 859–861. 1 indexed citations
16.
Funderburk, Steve J., Donald Guthrie, & David R. Meldrum. (1976). Suboptimal pregnancy outcome among women with prior abortions and premature births. American Journal of Obstetrics and Gynecology. 126(1). 55–60. 23 indexed citations
17.
Funderburk, Steve J.. (1976). Acne in Retarded Boy With Autosomal Chromosomal Abnormality. Archives of Dermatology. 112(6). 859–859. 6 indexed citations
18.
Funderburk, Steve J.. (1975). Offspring of subfertile parents. A preliminary survey.. PubMed. 20(2). 73–6. 11 indexed citations
19.
Funderburk, Steve J., Michel Philippart, George L. Dale, Stephen D. Cederbaum, & John K. Vyden. (1974). Priapism after Phenoxybenzamine in a Patient with Fabry's Disease. New England Journal of Medicine. 290(11). 630–631. 10 indexed citations
20.
Philippart, Michel, John K. Vyden, & Steve J. Funderburk. (1974). ABNORMAL PERIPHERAL BLOOD FLOW IN FABRY'S DISEASE: ITS RELATIONSHIP TO PAIN. Pediatric Research. 8(4). 393–393. 5 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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