Robin M. Winter

7.7k citations

57 papers · 5.2k indexed · 2 hit papers · h-index 30

Impact in

Genetics top 0.2%
- 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
Developmental Biology top 1%

Papers in

Developmental Biology 9
- Congenital limb and hand anomalies 9
Genetics 36
- Craniofacial Disorders and Treatments 13
- Genomic variations and chromosomal abnormalities 10
- Cleft Lip and Palate Research 8
- Connective tissue disorders research 7
- Genetics and Neurodevelopmental Disorders 7

Co-authors: William Reardon Paul Rutland Louise J. Pulleyn Sue Malcolm Andrew O.M. Wilkie Barry M. Jones Jonathan Flint Richard Hayward
Journals: Nature Genetics (9 papers)American Journal of Medical Genetics (16 papers)The Journal of Pediatrics (1 paper)European Journal of Human Genetics (1 paper)Human Molecular Genetics (1 paper)
Partner nations: United Kingdom United States Australia

In The Last Decade

Robin M. Winter

57 papers receiving 5.1k citations

Hit Papers

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome 1995 · 666 citations

Peers

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-authorship network

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

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20 of 20 papers shown

#	Work
1	G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex Science ·Xianhua Piao, R. Sean Hill, Adria Bodell, Bernard S. Chang, Lina Basel‐Vanagaite, Rachel Straussberg, William B. Dobyns, Anyes Taffard, Robin M. Winter, A. Micheil Innes, Thomas Voit, M. Elizabeth Ross, Jacques L. Michaud, 純幸西田, A. James Barkovich, Christopher A. Walsh	2004	405
2	3D analysis of facial morphology American Journal of Medical Genetics Part A ·Peter Hammond, Tim J. Hutton, Judith Allanson, Linda Campbell, Raoul C. M. Hennekam, Sean B. Holden, Michael A. Patton, Adam Shaw, I. Karen Temple, Matthew Trotter, Kieran C. Murphy, Robin M. Winter	2004	181
3	Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16 Annals of Neurology ·Bernard S. Chang, Xianhua Piao, Adria Bodell, Lina Basel‐Vanagaite, Rachel Straussberg, William B. Dobyns, Anyes Taffard, Robin M. Winter, A. Micheil Innes, Thomas Voit, P. Ellen Grant, A. James Barkovich, Marnelli Canlas	2003	100
4	Type 1 Arnold???Chiari malformation and Noonan syndrome. A new diagnostic feature? Clinical Dysmorphology ·Muriel Holder‐Espinasse, Robin M. Winter	2003	34
5	A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28 The American Journal of Human Genetics ·Laurent Villard, Karine Nguyen, Carlos Cardoso, Christa Lese Martin, Vasil Tchaban, Fatine Drhimer, Arthur W. Grix, John M. Graham, Robin M. Winter, Richard J. Leventer, William B. Dobyns	2002	79
6	Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus‐Merzbacher disease American Journal of Medical Genetics Part A ·Karen Woodward, Maria Cundall, Rodger Palmer, Robert Surtees, Robin M. Winter, Sue Malcolm	2002	12
7	Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13) American Journal of Medical Genetics ·Bert B.A. de Vries, Melissa Lees, Samantha J.L. Knight, Regina Regan, Daniela Arias Molinares, Jonathan Flint, Angela Barnicoat, Robin M. Winter	2001	18
8	Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients Clinical Dysmorphology ·Astrid S. Plomp, M Baraitser, Sarah F. Slaney, Robin M. Winter	2000	1
9	Subtle chromosomal rearrangements in children with unexplained mental retardation The Lancet ·Samantha J.L. Knight, Regina Regan, A Nicod, Sharon W. Horsley, Robert E. Kearney, Tessa Homfray, Robin M. Winter, Patrick Bolton, Jonathan Flint	1999	325
10	Hemihypertrophy, hemimegalencephaly, and polydactyly American Journal of Medical Genetics ·William Reardon, Brian Harding, Robin M. Winter, M Baraitser	1996	14
11	Analysing human developmental abnormalities BioEssays ·Robin M. Winter	1996	15
12	Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome Nature Genetics ·Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge, Michael D. Poole, Luis Guillermo Quintana, Anthony D. Hockley, Richard Hayward, David J. David, Louise J. Pulleyn, Paul Rutland, S Malcolm, Robin M. Winter, William Reardon Hit paper breakdown →	1995	666
13	Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes Nature Genetics ·Paul Rutland, Louise J. Pulleyn, William Reardon, M Baraitser, Richard Hayward, Barry M. Jones, Sue Malcolm, Robin M. Winter, Michael Oldridge, Sarah F. Slaney, Michael D. Poole, Andrew O.M. Wilkie	1995	343
14	A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome Nature Genetics ·Maximilian Muenke, Maria Urzedo, Andreas Hehr, Nathaniel H. Robin, H. Wolfgang Losken, Albert Schinzel, Louise J. Pulleyn, Paul Rutland, William Reardon, Sue Malcolm, Robin M. Winter	1994	466
15	MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM Nature Genetics ·Lieve Vits, Guy Van Camp, Paul Coucke, Erik Fransén, Kristel De Boulle, Edwin Reyniers, Bernhard Korn, Annemarie Poustka, Golder N. Wilson, Connie Schrander‐Stumpel, Robin M. Winter, Charles Schwartz, Patrick J. Willems	1994	110
16	A unique association of short stature, dysmorphic features, and speech impairment (Floating-harbor syndrome) The Journal of Pediatrics ·Paul Robinson, Mordechai Shohat, Robin M. Winter, Tebepah Tarilah, SEMRA SAZAK, Murray Feingold, Zvi Laron, D L Rimoin	1988	41
17	Greig cephalopolysyndactyly syndrome: A possible mouse homologue (Xt‐extra toes) American Journal of Medical Genetics ·Robin M. Winter, Susan Huson, David J. Prieur, James F. Reynolds	1988	44
18	A child with sclerocornea, short limbs, short stature, and distinct facial appearance American Journal of Medical Genetics ·Elizabeth M. Thompson, Robin M. Winter, John M. Opitz, James F. Reynolds	1988	9
19	Osteopathia striata with cranial sclerosis: Highly variable expression within a family including cleft palate in two neonatal cases Clinical Genetics ·Robin M. Winter, M D Crawfurd, Hylton B. Meire, B A Kogan	1980	29
20	Dominantly Inherited Amyotrophic Lateral Sclerosis (Motor Neuron Disease) VCU Scholars Compass (Virginia Commonwealth University) ·Jesús Rivas-Ceballos, Robin M. Winter, Edwin C. Myer, Walter E. Nance	1977	1

About Robin M. Winter

Robin M. Winter is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology and Cell Biology, having authored 57 papers that have together received 5.2k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (13 papers), Genomic variations and chromosomal abnormalities (10 papers), Congenital limb and hand anomalies (9 papers), Cleft Lip and Palate Research (8 papers), Connective tissue disorders research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (5 papers) and Hedgehog Signaling Pathway Studies (5 papers). The work is most often cited by research in Genetics (3.5k citations), Developmental Biology (225 citations), Molecular Biology (2.9k citations), Pediatrics, Perinatology and Child Health (554 citations) and Genetics (228 citations). Robin M. Winter has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include William Reardon, Paul Rutland, Louise J. Pulleyn, Sue Malcolm, Andrew O.M. Wilkie, Barry M. Jones, Jonathan Flint, Richard Hayward, Sarah F. Slaney and Michael Oldridge. Their work appears in journals such as Nature Genetics, American Journal of Medical Genetics, The Journal of Pediatrics, European Journal of Human Genetics and Human Molecular 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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