R M Winter

1.0k total citations
32 papers, 683 citations indexed

About

R M Winter is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, R M Winter has authored 32 papers receiving a total of 683 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 15 papers in Molecular Biology and 9 papers in Surgery. Recurrent topics in R M Winter's work include Craniofacial Disorders and Treatments (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cleft Lip and Palate Research (4 papers). R M Winter is often cited by papers focused on Craniofacial Disorders and Treatments (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cleft Lip and Palate Research (4 papers). R M Winter collaborates with scholars based in United Kingdom, Germany and India. R M Winter's co-authors include Albert Schinzel, Conny M.A. van Ravenswaaij‐Arts, S Malcolm, Murray Bain, William Reardon, T J David, Elizabeth M. Thompson, Helena M. Gardiner, Frances Elmslie and Anthony J. Vivian and has published in prestigious journals such as Human Molecular Genetics, Investigative Ophthalmology & Visual Science and Archives of Disease in Childhood.

In The Last Decade

R M Winter

32 papers receiving 663 citations

Peers

R M Winter

GENET

SURGE

PPCH

Victoria del Castillo Mexico

Michele Clemens United States

Georg Klaus Hinkel Germany

R. A. Pfeiffer Germany

Anita S. Kulharya United States

Satoru Sakazume Japan

Yolande van Bever Netherlands

Ernest Lieber United States

Marie‐France Portnoï France

Roy Wadey United Kingdom

Victoria del Castillo Mexico

R M Winter

427 ×1.1

GENET

244 ×0.9

113 ×0.7

SURGE

91 ×1.0

PPCH

68 ×0.9

Citations per year, relative to R M Winter R M Winter (= 1×) peers Victoria del Castillo

Countries citing papers authored by R M Winter

Since Specialization

Citations

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

Fields of papers citing papers by R M Winter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R M Winter

This figure shows the co-authorship network connecting the top 25 collaborators of R M Winter. A scholar is included among the top collaborators of R M 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 R M Winter. R M Winter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Crow, Yanick J., C. Geoffrey Woods, Manir Ali, et al.. (2004). Congenital glaucoma and brain stem atrophy as features of Aicardi–Goutières syndrome. American Journal of Medical Genetics Part A. 129A(3). 303–307. 28 indexed citations

Lindemann, S., Kenji Kamino, Dirk Wedekind, et al.. (2003). Histological Examination in a Blind-deafness Rat Mutant – A Rodent Model for Usher Syndrome Phenotype 1. Investigative Ophthalmology & Visual Science. 44(13). 2820–2820. 1 indexed citations

Lindemann, S., et al.. (2003). Retinitis Pigmentosa in Spontaneous Rat Mutants With Sensorineural Deafness and Vestibular Dysfunction – A Rodent Model for Usher Syndrome Phenotype 1. Investigative Ophthalmology & Visual Science. 44(13). 1861–1861. 4 indexed citations

Winter, R M, et al.. (2003). Telomeres: a diagnosis at the end of the chromosomes. Journal of Medical Genetics. 40(6). 385–398. 166 indexed citations

Winter, R M, et al.. (2003). Risikofaktorenanalyse und Therapievergleich zwischen Heparin und H�modilution bei Zentralarterienverschluss des Auges. Der Ophthalmologe. 100(10). 819–824. 6 indexed citations

Brady, Angela F., R M Winter, Louise C. Wilson, et al.. (2002). Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysis: a new autosomal recessive syndrome?. Clinical Dysmorphology. 11(3). 155–161. 13 indexed citations

Kelberman, Daniel, Jess Tyson, David Chandler, et al.. (2001). Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. Human Genetics. 109(6). 638–645. 92 indexed citations

Kelberman, Daniel, et al.. (2000). Mapping of a locus for autosomal dominant Hemifacial Microsomia. UCL Discovery (University College London). 1 indexed citations

Bitner‐Glindzicz, Maria, et al.. (2000). A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome. Clinical Genetics. 58(6). 483–487. 23 indexed citations

10.

Winter, R M, et al.. (1999). Further evidence from two families that craniofrontonasal dysplasia maps to Xp22. Clinical Genetics. 55(6). 473–477. 6 indexed citations

11.

Slaney, Sarah F., C. Michael Hall, David J. Atherton, & R M Winter. (1999). A new syndrome of spondyloepimetaphyseal dysplasia, eczema and hypogammaglobulinaemia. Clinical Dysmorphology. 5(2). 79???86–79???86. 4 indexed citations

12.

Slaney, Sarah F., W.K. Chong, & R M Winter. (1999). A new syndrome of short stature, distinctive facial features and periventricular grey matter heterotopia. Clinical Dysmorphology. 8(1). 5???10–5???10. 8 indexed citations

13.

Pulleyn, Louise J., William Reardon, David Wilkes, et al.. (1996). Spectrum of CraniosynostosisPhenotypes Associated with NovelMutations at the Fibroblast GrowthFactor Receptor 2 Locus. European Journal of Human Genetics. 4(5). 283–291. 62 indexed citations

14.

Winter, R M, et al.. (1996). Advances in genetics.. Archives of Disease in Childhood. 75(4). 346–350. 1 indexed citations

15.

Winter, R M. (1995). Recent molecular advances in dysmorphology. Human Molecular Genetics. 4(suppl_1). 1699–1704. 8 indexed citations

16.

Elmslie, Frances, et al.. (1995). Alagille syndrome: family studies.. Journal of Medical Genetics. 32(4). 264–268. 52 indexed citations

17.

Winter, R M & Elizabeth M. Thompson. (1982). Lethal, neonatal, short-limbed platyspondylic dwarfism. A further variant?. Human Genetics. 61(3). 269–272. 17 indexed citations

18.

Winter, R M. (1980). The calculation of genetic risks in X‐linked recessive conditions using programmable calculators. Clinical Genetics. 17(2). 171–175. 2 indexed citations

19.

Winter, R M. (1979). [Glomangioma in the eyelid. A clinical and histological case report (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 175(1). 107–9. 1 indexed citations

20.

McElfresh, Edward C. & R M Winter. (1973). Klippel-Feil syndrome.. PubMed. 56(5). 353–7. 7 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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