R H Lindenbaum

2.8k total citations
39 papers, 1.7k citations indexed

About

R H Lindenbaum is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, R H Lindenbaum has authored 39 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 16 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in R H Lindenbaum's work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (11 papers) and Genetics and Neurodevelopmental Disorders (4 papers). R H Lindenbaum is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (11 papers) and Genetics and Neurodevelopmental Disorders (4 papers). R H Lindenbaum collaborates with scholars based in United Kingdom, United States and India. R H Lindenbaum's co-authors include Martin Bobrow, Helen V. Firth, Patricia A. Boyd, Susan Huson, P. Chamberlain, Markku Ryynänen, Chirag Patel, Andrew O.M. Wilkie, Geoffrey D Clarke and John T. Hughes and has published in prestigious journals such as New England Journal of Medicine, Cell and The Lancet.

In The Last Decade

R H Lindenbaum

37 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R H Lindenbaum United Kingdom	20	960	715	529	253	192	39	1.7k
J P Fryns Belgium	25	1.2k 1.3×	1.1k 1.5×	430 0.8×	304 1.2×	190 1.0×	90	2.2k
Patricia A. Ward United States	25	1.2k 1.3×	1.0k 1.5×	627 1.2×	161 0.6×	152 0.8×	65	2.5k
C. T. R. M. Schrander‐Stumpel Netherlands	24	1.4k 1.4×	671 0.9×	411 0.8×	298 1.2×	93 0.5×	86	2.1k
Jaakko Leisti Finland	27	873 0.9×	1.1k 1.6×	267 0.5×	151 0.6×	103 0.5×	82	2.1k
Kwame Anyane‐Yeboa United States	26	1.2k 1.3×	1.3k 1.8×	361 0.7×	277 1.1×	222 1.2×	66	2.3k
Maureen Bocian United States	18	1.4k 1.5×	1.2k 1.7×	241 0.5×	247 1.0×	101 0.5×	35	2.1k
J Boué France	22	1.5k 1.6×	1.4k 2.0×	377 0.7×	175 0.7×	116 0.6×	82	2.6k
Ursula G. Froster Germany	23	886 0.9×	900 1.3×	371 0.7×	334 1.3×	74 0.4×	79	2.0k
Renata Laxová United States	19	623 0.6×	765 1.1×	289 0.5×	157 0.6×	74 0.4×	53	1.6k
Jean‐Pierre Fryns Belgium	18	635 0.7×	664 0.9×	185 0.3×	249 1.0×	82 0.4×	72	1.3k

Countries citing papers authored by R H Lindenbaum

Since Specialization

Citations

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

Fields of papers citing papers by R H Lindenbaum

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R H Lindenbaum

This figure shows the co-authorship network connecting the top 25 collaborators of R H Lindenbaum. A scholar is included among the top collaborators of R H Lindenbaum 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 H Lindenbaum. R H Lindenbaum 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

Dragoman, Monica, et al.. (2012). Unfulfilled sterilization requests: what happens 6 months later?. Contraception. 86(3). 323–323.

Ratcliffe, S G, et al.. (1994). Prenatal Testosterone Levels in XXY and XYY Males. Hormone Research. 42(3). 106–109. 39 indexed citations

Shelbourne, Peggy, June Davies, Jessica L. Buxton, et al.. (1993). Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker. New England Journal of Medicine. 328(7). 471–475. 58 indexed citations

Harvey, John F., et al.. (1993). Molecular studies of trisomy 18.. PubMed. 52(6). 1139–44. 38 indexed citations

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

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

Firth, Helen V., et al.. (1991). Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation. The Lancet. 337(8744). 762–763. 238 indexed citations

Evans, D. Gareth, et al.. (1990). Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndrome.. Journal of Medical Genetics. 27(11). 720–721. 6 indexed citations

Shiwach, Raj S. & R H Lindenbaum. (1990). Prevalence of Huntington's Disease Among Uk. The British Journal of Psychiatry. 157(4). 598–599. 21 indexed citations

10.

Lygidakis, N. Α. & R H Lindenbaum. (1989). Oral fibromatosis in tuberous sclerosis. Oral Surgery Oral Medicine Oral Pathology. 68(6). 725–728. 38 indexed citations

11.

Lamb, Janette, R H Lindenbaum, Stephen T. Reeders, et al.. (1989). DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE. The Lancet. 334(8667). 819–824. 71 indexed citations

12.

WEST, L. F., et al.. (1988). Regional assignment of the gene coding for human sucrase‐isomaltase (SI) to chromosome 3q25‐26. Annals of Human Genetics. 52(1). 57–61. 13 indexed citations

13.

Young, I D, R H Lindenbaum, Elizabeth M. Thompson, & Marcus Pembrey. (1985). Amniotic bands in connective tissue disorders.. Archives of Disease in Childhood. 60(11). 1061–1063. 44 indexed citations

14.

Terzian, Emanuela, Jillian Boreham, Howard Cuckle, et al.. (1985). A survey of diagnostic amniocenteses in Oxford from 1974–1981. Prenatal Diagnosis. 5(6). 401–414. 16 indexed citations

15.

Madan, K., M. Seabright, R H Lindenbaum, & Martin Bobrow. (1984). Paracentric inversions in man.. Journal of Medical Genetics. 21(6). 407–412. 39 indexed citations

16.

Cook, P.J.L., R H Lindenbaum, Riitta Salonen, et al.. (1981). The MNSs blood groups of families with chromosome 4 rearrangements. Annals of Human Genetics. 45(1). 39–47. 23 indexed citations

17.

Lindenbaum, R H, Geoffrey D Clarke, Chirag Patel, Marc Moncrieff, & John T. Hughes. (1979). Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.. Journal of Medical Genetics. 16(5). 389–392. 128 indexed citations

18.

Smith, Robin, R H Lindenbaum, & R. J. Walton. (1976). Hypophosphataemic Osteomalacia and Fanconi Syndrome of Adult Onset with Dominant Inheritance<subtitle>POSSIBLE RELATIONSHIP WITH DIABETES MELLITUS</subtitle>. QJM. 45(179). 387–400. 12 indexed citations

19.

Lindenbaum, R H, et al.. (1973). Two cases of endocardial fibroelastosis--possible x-linked determination.. Heart. 35(1). 38–40. 14 indexed citations

20.

Lindenbaum, R H, et al.. (1973). HARE-LIP IN LARSEN'S SYNDROME. The Lancet. 301(7798). 318–318. 4 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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