Robin M. Winter

7.8k citations
70 papers · 6.5k · 2 hit papers · h-index 33

Impact in

  • Genetics top 0.5%
    • Craniofacial Disorders and Treatments
    • Cleft Lip and Palate Research
    • Genomic variations and chromosomal abnormalities
    • Connective tissue disorders research
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Craniofacial Disorders and Treatments 16
    • Genomic variations and chromosomal abnormalities 10
    • Cleft Lip and Palate Research 10
    • Connective tissue disorders research 7
    • Genetics and Neurodevelopmental Disorders 6
    • Congenital limb and hand anomalies 9

Robin M. Winter

69 papers receiving 6.1k citations

Robin M. Winter's Hit Papers

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome 1995 · 768 citations
7680+10+21Years since publication250500750

Peers

Robin M. Winter
Comparison fields: 5 of 131
  • Genetics 4.1k
  • Developmental Biology 245
  • Molecular Biology 3.2k
  • Pediatrics, Perinatology and Child Health 622
  • Genetics 334
Replace Beate Albrecht with:
Beate Albrecht Germany
Ruth A Newbury-Ecob United Kingdom
Alan E Fryer United Kingdom
Ernie M.H.F. Bongers Netherlands
Han G. Brunner Netherlands
Gabriele Gillessen‐Kaesbach Germany
J. P. Fryns Belgium
Albert David France
Arie van Haeringen Netherlands
Nurten Ayse Akarsu Türkiye
Robin M. Winter relative to Beate Albrecht Germany Beate Albrecht's profile →
Citations per field
00.5×1.5×
Beate Albrecht · 1×
Citations per year

Countries citing papers authored by Robin M. Winter

Since Specialization
Citations

This map shows the geographic impact of Robin M. 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 M. 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 M. Winter more than expected).

Fields of papers citing papers by Robin M. Winter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Robin M. Winter, 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 Robin M. Winter Line = papers co-authored together Robin M. Winter links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 70 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
Hit paper breakdown →
1995768
2
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
Hit paper breakdown →
1994645
3 1994540
4 2004447
5 1995424
6 1995390
7 1999371
8 1998269
9 1997250
10 2003213
11 2004202
12 2001173
13 1998147
14 1994123
15 2003118
16 200296
17 199884
18 199359
19 199659
20 200357

About Robin M. Winter

Robin M. Winter is a scholar working on Genetics, Developmental Biology, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 70 papers that have together received 6.5k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (16 papers), Genomic variations and chromosomal abnormalities (10 papers), Cleft Lip and Palate Research (10 papers), Congenital limb and hand anomalies (9 papers), Congenital Anomalies and Fetal Surgery (7 papers), Connective tissue disorders research (7 papers), Hedgehog Signaling Pathway Studies (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). The work is most often cited by research in Genetics (4.1k citations), Developmental Biology (245 citations), Molecular Biology (3.2k citations), Pediatrics, Perinatology and Child Health (622 citations) and Genetics (334 citations). Robin M. Winter has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include William Reardon, Paul Rutland, Louise J. Pulleyn, Sue Malcolm, Andrew O.M. Wilkie, Barry M. Jones, Jonathan Flint, Sarah F. Slaney, Richard D Hayward and Michael Drury Poole. Their work appears in journals such as Nature Genetics, The Lancet, American Journal of Medical Genetics, Clinical Genetics and Journal of Medical Genetics.

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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