M Baraitser

7.8k total citations
198 papers, 5.1k citations indexed

About

M Baraitser is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, M Baraitser has authored 198 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 86 papers in Genetics, 67 papers in Molecular Biology and 39 papers in Surgery. Recurrent topics in M Baraitser's work include Connective tissue disorders research (21 papers), Congenital limb and hand anomalies (17 papers) and Craniofacial Disorders and Treatments (17 papers). M Baraitser is often cited by papers focused on Connective tissue disorders research (21 papers), Congenital limb and hand anomalies (17 papers) and Craniofacial Disorders and Treatments (17 papers). M Baraitser collaborates with scholars based in United Kingdom, Canada and India. M Baraitser's co-authors include R M Winter, Jorge Saraiva, Jane A. Hurst, John Burn, I. Karen Temple, Robin M. Winter, William Reardon, M A Patton, E M Brett and Christine Oley and has published in prestigious journals such as Nature Genetics, Brain and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

M Baraitser

193 papers receiving 4.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M Baraitser United Kingdom	36	2.5k	2.3k	789	720	541	198	5.1k
Frank Greenberg United States	44	3.8k 1.5×	3.1k 1.4×	901 1.1×	1.3k 1.8×	818 1.5×	112	7.2k
Joël Zlotogora Israel	35	2.0k 0.8×	1.9k 0.9×	381 0.5×	690 1.0×	400 0.7×	170	5.0k
John M. Optiz United States	38	2.4k 0.9×	2.1k 0.9×	714 0.9×	1.0k 1.4×	376 0.7×	155	5.1k
Lionel Van Maldergem Belgium	41	2.1k 0.8×	3.8k 1.7×	655 0.8×	333 0.5×	526 1.0×	153	6.9k
Lisbeth Tranebjærg Denmark	43	2.3k 0.9×	3.6k 1.6×	415 0.5×	468 0.7×	349 0.6×	163	6.7k
Dian Donnai United Kingdom	48	3.0k 1.2×	3.1k 1.4×	1.1k 1.4×	1.2k 1.7×	418 0.8×	177	7.8k
Niklas Dahl Sweden	50	2.9k 1.1×	5.9k 2.6×	957 1.2×	465 0.6×	469 0.9×	245	9.8k
Michel Vekemans France	44	3.3k 1.3×	4.1k 1.8×	1.2k 1.6×	1.7k 2.3×	439 0.8×	248	8.7k
Anita Rauch Germany	48	3.4k 1.4×	4.4k 1.9×	617 0.8×	679 0.9×	283 0.5×	194	7.5k
M. Leppert United States	40	1.4k 0.5×	2.8k 1.2×	658 0.8×	216 0.3×	602 1.1×	169	6.1k

Countries citing papers authored by M Baraitser

Since Specialization

Citations

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

Fields of papers citing papers by M Baraitser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Baraitser

This figure shows the co-authorship network connecting the top 25 collaborators of M Baraitser. A scholar is included among the top collaborators of M Baraitser 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 M Baraitser. M Baraitser 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

Kaissi, Ali Al, et al.. (2003). Siblings with glaucoma, mental retardation and short stature. Clinical Dysmorphology. 12(3). 191–194. 5 indexed citations

Plomp, Astrid S., M Baraitser, Sarah F. Slaney, & Robin M. Winter. (2000). Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients. Clinical Dysmorphology. 9(1). 11–14. 1 indexed citations

Lees, Melissa, P R Hodgkins, William Reardon, et al.. (1998). Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases. Clinical Dysmorphology. 7(3). 157–162. 26 indexed citations

Chitty, Lyn S., S. Robb, Carolyn A. Berry, David M. Silver, & M Baraitser. (1996). PEHO or PEHO-like syndrome?. Clinical Dysmorphology. 5(2). 143–152. 22 indexed citations

Reardon, William, Richard J. Gibbons, R M Winter, & M Baraitser. (1995). Male pseudohermaphroditism in sibs with the α‐thalassemia/mental retardation (ATR‐X) syndrome. American Journal of Medical Genetics. 55(3). 285–287. 25 indexed citations

Reardon, William, C. Michael Hall, Sarah F. Slaney, et al.. (1993). Mesomelic limb shortness: A previously unreported autosomal recessive type. American Journal of Medical Genetics. 47(5). 788–792. 8 indexed citations

Reardon, William, et al.. (1991). Atypical facio‐scapulo‐humeral muscular dystrophy — a counselling dilemma. Clinical Genetics. 39(3). 172–177. 2 indexed citations

Levy, Philip T. & M Baraitser. (1991). Coffin-Siris syndrome.. Journal of Medical Genetics. 28(5). 338–341. 37 indexed citations

Scheffer, Ingrid E., M Baraitser, & E M Brett. (1991). Severe Microcephaly Associated with Congenital Varicella Infection. Developmental Medicine & Child Neurology. 33(10). 916–920. 16 indexed citations

10.

Reardon, William, I. Karen Temple, Barry M. Jones, & M Baraitser. (1990). Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?. Clinical Genetics. 38(3). 233–236. 10 indexed citations

11.

Harbord, Michael, et al.. (1990). Megalencephaly with Dysmyelination, Spasticity, Ataxia, Seizures and Distinctive Neurophysiological Findings in Two Siblings. Neuropediatrics. 21(3). 164–168. 31 indexed citations

12.

Harbord, Michael, et al.. (1990). Ataxia, Developmental Delay and an Extensive Neuronal Migration Abnormality in 2 Siblings. Neuropediatrics. 21(4). 218–221. 25 indexed citations

13.

Hurst, Jane A., R M Winter, M Baraitser, John M. Optiz, & James F. Reynolds. (1988). Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed ears. American Journal of Medical Genetics. 29(1). 107–115. 17 indexed citations

14.

Baraitser, M. (1987). The Chromosomes and Their Disorders 4th ed.. Journal of Neurology Neurosurgery & Psychiatry. 50(6). 828–828.

15.

Baraitser, M, et al.. (1987). Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis. Pediatric Neurology. 3(6). 360–362. 18 indexed citations

16.

Patton, M A, et al.. (1987). Congenital cutis laxa with retardation of growth and development.. Journal of Medical Genetics. 24(9). 556–561. 29 indexed citations

17.

Winter, R M, et al.. (1984). A computerised data base for the diagnosis of rare dysmorphic syndromes.. Journal of Medical Genetics. 21(2). 121–123. 66 indexed citations

18.

Evans, K., et al.. (1983). Effect of genetic counselling on the prevalence of Huntington's chorea.. BMJ. 286(6361). 281–283. 17 indexed citations

19.

Burn, John, M Baraitser, & L. J. Butler. (1983). An avoidable recurrence of cri du chat syndrome in the next generation.. BMJ. 287(6401). 1287–1288. 15 indexed citations

20.

Baraitser, M. (1978). Down's Anomaly 2nd ed. Journal of Medical Genetics. 15(1). 79.1–79. 15 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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