Meinhard Robinow

2.9k total citations
70 papers, 1.7k citations indexed

About

Meinhard Robinow is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Meinhard Robinow has authored 70 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 16 papers in Molecular Biology and 11 papers in Surgery. Recurrent topics in Meinhard Robinow's work include Congenital limb and hand anomalies (10 papers), Craniofacial Disorders and Treatments (7 papers) and Connective tissue disorders research (5 papers). Meinhard Robinow is often cited by papers focused on Congenital limb and hand anomalies (10 papers), Craniofacial Disorders and Treatments (7 papers) and Connective tissue disorders research (5 papers). Meinhard Robinow collaborates with scholars based in United States, Australia and Canada. Meinhard Robinow's co-authors include John M. Opitz, Gerald Johnson, James F. Reynolds, Virginia V. Michels, Dawna Armstrong, Cynthia J. Curry, Lewis B. Holmes, Arthur Grix, Roberta A Pagon and Renata Laxová and has published in prestigious journals such as New England Journal of Medicine, PEDIATRICS and Radiology.

In The Last Decade

Meinhard Robinow

68 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Meinhard Robinow United States 21 781 599 243 229 128 70 1.7k
R. Neil Schimke United States 27 882 1.1× 699 1.2× 418 1.7× 207 0.9× 104 0.8× 76 2.4k
Mark Lubinsky United States 25 734 0.9× 577 1.0× 399 1.6× 401 1.8× 91 0.7× 73 1.6k
Jaakko Leisti Finland 27 1.1k 1.4× 873 1.5× 151 0.6× 267 1.2× 156 1.2× 82 2.1k
Naomi Fitch Canada 22 479 0.6× 585 1.0× 262 1.1× 186 0.8× 67 0.5× 44 1.1k
Eva Sujansky United States 19 969 1.2× 781 1.3× 447 1.8× 342 1.5× 248 1.9× 30 2.0k
Y. Gillerot Belgium 22 740 0.9× 616 1.0× 334 1.4× 426 1.9× 83 0.6× 74 1.8k
M. H. K. Shokeir Canada 19 557 0.7× 355 0.6× 191 0.8× 178 0.8× 60 0.5× 48 1.3k
Lester Weiss United States 29 918 1.2× 1.4k 2.3× 215 0.9× 448 2.0× 51 0.4× 82 2.3k
Yoshikazu Kuroki Japan 26 835 1.1× 1.4k 2.4× 284 1.2× 400 1.7× 71 0.6× 106 2.2k
Helen Kingston United Kingdom 24 839 1.1× 645 1.1× 122 0.5× 161 0.7× 117 0.9× 63 1.9k

Countries citing papers authored by Meinhard Robinow

Since Specialization
Citations

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

Fields of papers citing papers by Meinhard Robinow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meinhard Robinow

This figure shows the co-authorship network connecting the top 25 collaborators of Meinhard Robinow. A scholar is included among the top collaborators of Meinhard Robinow 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 Meinhard Robinow. Meinhard Robinow 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.
Byers, Peter H., Madeleine Duvic, Mary Atkinson, et al.. (1997). Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in theCOL1A1 andCOL1A2 genes of type I collagen. American Journal of Medical Genetics. 72(1). 94–105. 82 indexed citations
2.
Robinow, Meinhard, et al.. (1995). Femoral‐facial syndrome–prenatal diagnosis–autosomal dominant inheritance. American Journal of Medical Genetics. 57(3). 397–399. 28 indexed citations
3.
Robinow, Meinhard. (1995). Living history—autobiography: Pediatric genetics in a new world. American Journal of Medical Genetics. 59(1). 8–13.
4.
Robinow, Meinhard. (1991). Respiratory obstruction and cor pulmonale in the Hallermann‐Streiff syndrome. American Journal of Medical Genetics. 41(4). 515–516. 9 indexed citations
5.
Charrow, Joel, et al.. (1991). Autosomal recessive cerebellar hypoplasia and endosteal sclerosis: A newly recognized syndrome. American Journal of Medical Genetics. 41(4). 464–468. 14 indexed citations
6.
Robinow, Meinhard, et al.. (1989). Secondary trisomy or mosaic “tetrasomy” 8p. American Journal of Medical Genetics. 32(3). 320–324. 20 indexed citations
7.
Dobyns, William B., Roberta A Pagon, Dawna Armstrong, et al.. (1989). Diagnostic criteria for Walker‐Warburg syndrome. American Journal of Medical Genetics. 32(2). 195–210. 313 indexed citations
8.
Robinow, Meinhard, Gerald Johnson, & John M. Optiz. (1988). The Weismann‐Netter syndrome. American Journal of Medical Genetics. 29(3). 573–579. 10 indexed citations
9.
Hoyme, H. Eugene, et al.. (1987). Autosomal dominant ectrodactyly and absence of long bones of upper or lower limbs: Further clinical delineation. The Journal of Pediatrics. 111(4). 538–543. 18 indexed citations
10.
Butler, Merlin G., F. John Meaney, William B. Wadlington, et al.. (1987). Metacarpophalangeal pattern profile analysis in Robinow syndrome. American Journal of Medical Genetics. 27(1). 219–223. 28 indexed citations
11.
Robinow, Meinhard, et al.. (1986). Hemifacial microsomia, ipsilateral facial palsy, and malformed auricle in two families: An autosomal dominant malformation. American Journal of Medical Genetics. 25(S2). 129–133. 19 indexed citations
12.
Butler, Merlin G., et al.. (1985). Metacarpophalangeal pattern profile analysis in Robinow syndrome. PMC. 5 indexed citations
13.
Lane, R., Meinhard Robinow, & Allen D. Roses. (1983). The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.. Journal of Medical Genetics. 20(1). 1–11. 22 indexed citations
14.
Robinow, Meinhard, Gerald Johnson, & John M. Opitz. (1981). The Gordon syndrome: Autosomal dominant cleft palate, camptodactyly, and club feet. American Journal of Medical Genetics. 9(2). 139–146. 11 indexed citations
15.
Robinow, Meinhard, et al.. (1980). Turner syndrome: sonography showing fetal hydrops simulating hydramnios. American Journal of Roentgenology. 135(4). 846–848. 12 indexed citations
16.
Robinow, Meinhard, et al.. (1978). Discordance in monozygotic twins for aglossia-adactylia, and possible clues to the pathogenesis of the syndrome.. PubMed. 14(6A). 223–30. 15 indexed citations
17.
Robinow, Meinhard. (1976). Mental retardation in Duchenne muscular dystrophy: Its relation to the maternal carrier state. The Journal of Pediatrics. 88(5). 896–897. 5 indexed citations
18.
Robinow, Meinhard, et al.. (1975). Acrocephalopolysyndactyly, type Noack, in a large kindred.. PubMed. 11(5). 99–106. 19 indexed citations
19.
Robinow, Meinhard. (1965). Fusobacterium Bacteremia in the Newborn. Archives of Pediatrics and Adolescent Medicine. 110(1). 92–92. 9 indexed citations
20.
Robinow, Meinhard. (1963). Diphenylhydantoin Hypersensitivity. American journal of diseases of children. 106(6). 553–553. 13 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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