Robert F. Stratton

2.2k total citations
42 papers, 1.4k citations indexed

About

Robert F. Stratton is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Robert F. Stratton has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 20 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Robert F. Stratton's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers) and Hedgehog Signaling Pathway Studies (5 papers). Robert F. Stratton is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers) and Hedgehog Signaling Pathway Studies (5 papers). Robert F. Stratton collaborates with scholars based in United States, Netherlands and United Kingdom. Robert F. Stratton's co-authors include William B. Dobyns, Frank Greenberg, David H. Ledbetter, Robert L. Nussbaum, Julie T. Parke, Susan Airhart, Charleen M. Moore, Barbara R. DuPont, Jannine D. Cody and Erich Roessler and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The Journal of Pediatrics.

In The Last Decade

Robert F. Stratton

41 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert F. Stratton United States 19 916 736 353 144 138 42 1.4k
Ellen Magenis United States 18 815 0.9× 694 0.9× 191 0.5× 154 1.1× 245 1.8× 31 1.4k
Roberto Ciccone Italy 23 956 1.0× 681 0.9× 283 0.8× 270 1.9× 63 0.5× 51 1.4k
Armand Bottani Switzerland 24 1.3k 1.4× 1.2k 1.7× 302 0.9× 81 0.6× 107 0.8× 62 2.2k
Līvija Medne United States 25 928 1.0× 1.1k 1.5× 342 1.0× 141 1.0× 188 1.4× 53 1.8k
Mitsuo Masuno Japan 21 1.1k 1.2× 1.4k 1.9× 180 0.5× 138 1.0× 100 0.7× 86 2.3k
Erica Andersen United States 16 773 0.8× 612 0.8× 340 1.0× 85 0.6× 80 0.6× 28 1.5k
Gotthold Barbi Germany 17 632 0.7× 560 0.8× 188 0.5× 127 0.9× 105 0.8× 59 1.1k
H. Enders Germany 18 933 1.0× 899 1.2× 313 0.9× 99 0.7× 37 0.3× 40 1.5k
Teresa Mattina Italy 18 839 0.9× 764 1.0× 181 0.5× 172 1.2× 81 0.6× 59 1.4k
Jean‐Pierre Fryns Belgium 18 635 0.7× 664 0.9× 185 0.5× 82 0.6× 101 0.7× 72 1.3k

Countries citing papers authored by Robert F. Stratton

Since Specialization
Citations

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

Fields of papers citing papers by Robert F. Stratton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert F. Stratton. 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 Robert F. Stratton. The network helps show where Robert F. Stratton may publish in the future.

Co-authorship network of co-authors of Robert F. Stratton

This figure shows the co-authorship network connecting the top 25 collaborators of Robert F. Stratton. A scholar is included among the top collaborators of Robert F. Stratton 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 Robert F. Stratton. Robert F. Stratton 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.
Cody, Jannine D., Bridgette Soileau, Patricia Heard, et al.. (2013). Establishing a reference group for distal 18q-: clinical description and molecular basis. Human Genetics. 133(2). 199–209. 39 indexed citations
2.
Stratton, Robert F., et al.. (2012). Metastatic medulloblastoma in an adolescent with Simpson–Golabi–Behmel syndrome. American Journal of Medical Genetics Part A. 158A(10). 2534–2536. 18 indexed citations
3.
Ming, Jeffrey E., Erich Roessler, Han G. Brunner, et al.. (2002). Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Human Genetics. 110(4). 297–301. 174 indexed citations
4.
Lehman, Donna M., W.E. Sponsel, Robert F. Stratton, et al.. (2001). Genetic mapping of a novel X-linked recessive colobomatous microphthalmia. American Journal of Medical Genetics. 101(2). 114–119. 16 indexed citations
5.
Cody, Jannine D., Patricia D. Ghidoni, Barbara R. DuPont, et al.. (1999). Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. American Journal of Medical Genetics. 85(5). 455–462. 87 indexed citations
6.
Stratton, Robert F., et al.. (1998). Second 46,XX male with MLS syndrome. American Journal of Medical Genetics. 76(1). 37–41. 21 indexed citations
7.
Stratton, Robert F., et al.. (1997). Frontonasal malformation with tetralogy of Fallot associated with a submicroscopic deletion of 22q11. American Journal of Medical Genetics. 69(3). 287–289. 12 indexed citations
8.
Dobyns, William B., M A Patton, Robert F. Stratton, et al.. (1996). Cobblestone Lissencephaly with Normal Eyes and Muscle. Neuropediatrics. 27(2). 70–75. 32 indexed citations
9.
Stratton, Robert F., Barbara R. DuPont, Anne S. Olsen, et al.. (1995). Interstitial duplication 19p. American Journal of Medical Genetics. 57(4). 562–564. 12 indexed citations
10.
DuPont, Barbara R., et al.. (1994). Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization. American Journal of Medical Genetics. 50(1). 21–27. 24 indexed citations
11.
Stratton, Robert F., et al.. (1994). Deletion (11)(q14.1q21). American Journal of Medical Genetics. 49(3). 294–298. 15 indexed citations
12.
Stratton, Robert F., et al.. (1994). Deletion 5q35.3. American Journal of Medical Genetics. 51(2). 150–152. 24 indexed citations
13.
Stratton, Robert F., et al.. (1993). Possible second case of tricho‐oculo‐dermo‐vertebral (Alves) syndrome. American Journal of Medical Genetics. 46(3). 313–315. 5 indexed citations
14.
Stratton, Robert F., Barbara R. DuPont, Vicki Mattern, Robert L. Schelonka, & Charleen M. Moore. (1993). Interstitial Duplication of 7(q22→q34). American Journal of Medical Genetics. 47(3). 380–382. 9 indexed citations
15.
Stratton, Robert F., et al.. (1993). Trisomy 22 confirmed by fluorescent in situ hybridization. American Journal of Medical Genetics. 46(1). 109–112. 13 indexed citations
16.
Stratton, Robert F. & Robert Patterson. (1993). DNA confirmation of congenital myotonic dystrophy in non‐immune hydrops fetalis. Prenatal Diagnosis. 13(11). 1027–1030. 14 indexed citations
17.
Stratton, Robert F., et al.. (1993). Brachydactyly, mesomelia, mental retardation, aortic dilatation, mitral valve prolapse, and characteristic face. American Journal of Medical Genetics. 46(2). 138–141. 5 indexed citations
18.
Stratton, Robert F., et al.. (1993). Fryns syndrome. American Journal of Medical Genetics. 45(5). 562–564. 19 indexed citations
19.
Stratton, Robert F., et al.. (1992). Deletion of the proximal short arm of chromosome 8. American Journal of Medical Genetics. 42(1). 15–18. 9 indexed citations
20.
Stratton, Robert F., Brendan Lee, & Francesco Ramirez. (1991). Marshall syndrome. American Journal of Medical Genetics. 41(1). 35–38. 8 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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