Robin Winter

2.5k total citations
30 papers, 1.5k citations indexed

About

Robin Winter is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Robin Winter has authored 30 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Surgery. Recurrent topics in Robin Winter's work include Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). Robin Winter is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). Robin Winter collaborates with scholars based in United Kingdom, United States and Italy. Robin Winter's co-authors include William Reardon, Sue Malcolm, Brunella Franco, Andrea Ballabio, Yutaka Nakahori, Mark C. Hirst, A. Roche, Kay E. Davies, R H Lindenbaum and U. Froster‐Iskenius and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Bioinformatics.

In The Last Decade

Robin Winter

29 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robin Winter United Kingdom 15 931 882 166 151 146 30 1.5k
N R Dennis United Kingdom 20 628 0.7× 793 0.9× 157 0.9× 84 0.6× 152 1.0× 32 1.3k
Maureen Bocian United States 18 1.2k 1.3× 1.4k 1.6× 101 0.6× 128 0.8× 167 1.1× 35 2.1k
Ewa Obersztyn Poland 19 692 0.7× 711 0.8× 170 1.0× 124 0.8× 86 0.6× 78 1.2k
Gholamali Tariverdian Germany 18 721 0.8× 812 0.9× 76 0.5× 104 0.7× 77 0.5× 64 1.3k
Peter M. Kroisel Austria 16 935 1.0× 658 0.7× 172 1.0× 85 0.6× 83 0.6× 38 1.5k
Jean‐Pierre Fryns Belgium 18 664 0.7× 635 0.7× 82 0.5× 83 0.5× 182 1.2× 72 1.3k
Mitsuo Masuno Japan 21 1.4k 1.5× 1.1k 1.2× 138 0.8× 99 0.7× 82 0.6× 86 2.3k
Keiko Wakui Japan 28 1.3k 1.4× 1.4k 1.6× 353 2.1× 190 1.3× 73 0.5× 89 2.3k
Bert H.J. Eussen Netherlands 12 1.7k 1.9× 572 0.6× 355 2.1× 132 0.9× 117 0.8× 23 2.2k
Palma Finelli Italy 29 1.2k 1.3× 1.0k 1.2× 466 2.8× 79 0.5× 78 0.5× 95 2.2k

Countries citing papers authored by Robin Winter

Since Specialization
Citations

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

Fields of papers citing papers by Robin Winter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robin Winter

This figure shows the co-authorship network connecting the top 25 collaborators of Robin Winter. A scholar is included among the top collaborators of Robin Winter 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 Robin Winter. Robin Winter 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.
Winter, Robin, et al.. (2011). Increasing Timely and Available Prenatal Studies by Electronic Health Records. The Journal of the American Board of Family Medicine. 24(4). 344–350. 9 indexed citations
2.
Maurer, Gerald, et al.. (2008). Diagnostik und Therapie fetaler Nieren- und Harnwegsfehlbildungen. Ultraschall in der Medizin - European Journal of Ultrasound. 6(4). 173–181.
3.
Winter, Robin, et al.. (2004). Human–Mouse Gene Searcher: a tool to assist discovery of malformation-associated genes by using phenotype databases. Bioinformatics. 21(3). 408–409. 4 indexed citations
4.
Hitchins, Megan P., Sarah Rickard, Fatima Dhalla, et al.. (2003). Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS. American Journal of Medical Genetics Part A. 125A(2). 167–172. 39 indexed citations
5.
Falco, Francesca De, Silvia Cainarca, Grazia Andolfi, et al.. (2003). X‐linked Opitz syndrome: Novel mutations in the MID1 gene and redefinition of the clinical spectrum. American Journal of Medical Genetics Part A. 120A(2). 222–228. 72 indexed citations
6.
Ferrante, Maria Immacolata, Sally Feather, Alessandro Bulfone, et al.. (2001). Identification of the Gene for Oral-Facial-Digital Type I Syndrome. The American Journal of Human Genetics. 68(3). 569–576. 239 indexed citations
7.
8.
Goodman, Frances R., et al.. (1998). Deletions in HOXD13 Segregate with an Identical, Novel Foot Malformation in Two Unrelated Families. The American Journal of Human Genetics. 63(4). 992–1000. 79 indexed citations
9.
10.
Paavola, Paulina, Riitta Salonen, Alessandra Baumer, et al.. (1997). Clinical and genetic heterogeneity in Meckel syndrome. Human Genetics. 101(1). 88–92. 37 indexed citations
11.
Ramer, Jeanette C., Angela E. Lin, William B. Dobyns, et al.. (1995). Previously apparently undescribed syndrome: Shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation. American Journal of Medical Genetics. 57(3). 403–409. 82 indexed citations
12.
Tassabehji, Mayada, Valerie Newton, Angela F. Brady, et al.. (1995). The mutational spectrum in Waardenburg syndrome. Human Molecular Genetics. 4(11). 2131–2137. 172 indexed citations
13.
Reardon, William, Stewart Boyd, M. Pitt, John Wilson, & Robin Winter. (1994). Disordered Peripheral Nerve Conduction in DOOR(S) Syndrome. Neuropediatrics. 25(1). 33–35. 3 indexed citations
14.
Knight, Samantha J.L., Mark C. Hirst, A. Roche, et al.. (1992). Molecular studies of the fragile X syndrome. American Journal of Medical Genetics. 43(1-2). 217–223. 17 indexed citations
15.
Bell, M.V., Mark C. Hirst, Yutaka Nakahori, et al.. (1991). Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome. Cell. 64(4). 861–866. 287 indexed citations
16.
Winter, Robin. (1991). Holoprosencephaly — An overview and atlas of cases. Early Human Development. 25(1). 65–65. 6 indexed citations
17.
Baraitser, M, Kiyotaka Tomiwa, Jayne S. Wilson, & Robin Winter. (1989). A database of genetically determined neurological conditions for clinicians.. Journal of Neurology Neurosurgery & Psychiatry. 52(1). 106–107. 3 indexed citations
18.
Lau, YL, R J Levinsky, S Malcolm, et al.. (1988). Genetic prediction in X‐linked agammaglobulinaemia. American Journal of Medical Genetics. 31(2). 437–448. 16 indexed citations
19.
Winter, Robin, et al.. (1986). A new category of lethal short‐limbed dwarfism. American Journal of Medical Genetics. 25(1). 41–46. 9 indexed citations
20.
Harper, Peter S., Marcus Pembrey, E. Rhys Davies, et al.. (1983). Abstracts of the meeting of the Clinical Genetics Society held on 7 and 8 April 1983 at the University of Cambridge. Journal of Medical Genetics. 20(6). 454–458. 2 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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