M Baraitser

7.8k citations
198 papers · 5.1k · h-index 36

Impact in

  • Genetics top 0.5%
    • Craniofacial Disorders and Treatments
    • Cleft Lip and Palate Research
    • Genetics and Neurodevelopmental Disorders
    • Connective tissue disorders research
    • Genomic variations and chromosomal abnormalities

Papers in

    • Connective tissue disorders research 21
    • Craniofacial Disorders and Treatments 17
    • Neurogenetic and Muscular Disorders Research 16
    • Cleft Lip and Palate Research 12
    • Hedgehog Signaling Pathway Studies 11

M Baraitser

193 papers receiving 4.8k citations

Peers

M Baraitser
Comparison fields: 5 of 137
  • Developmental Biology 232
  • Genetics 2.5k
  • Genetics 541
  • Pediatrics, Perinatology and Child Health 720
  • Molecular Biology 2.3k
Replace J. P. Fryns with:
J. P. Fryns Belgium
Dian Donnai United Kingdom
Frank Greenberg United States
Alain Verloès France
John M. Optiz United States
Michel Vekemans France
Joël Zlotogora Israel
Ben C.J. Hamel Netherlands
Martine Le Merrer France
Lionel Van Maldergem Belgium
M Baraitser relative to J. P. Fryns Belgium J. P. Fryns's profile →
Citations per field
00.5×1.5×1.9×
J. P. Fryns · 1×
Citations per year

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-authors

The 25 scholars most cited alongside M Baraitser, 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 M Baraitser Line = papers co-authored together M Baraitser links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 198 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1995343
2 1990238
3 1992208
4 1982173
5 1982138
6 198898
7 198787
8 199086
9 198880
10 198076
11 198267
12 198466
13 198764
14 197763
15 198961
16 198855
17 197554
18 199054
19 199353
20 198050

About M Baraitser

M Baraitser is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Developmental Biology, having authored 198 papers that have together received 5.1k indexed citations. Recurring topics across this work include Connective tissue disorders research (21 papers), Craniofacial Disorders and Treatments (17 papers), Congenital limb and hand anomalies (17 papers), Neurogenetic and Muscular Disorders Research (16 papers), Genetic Neurodegenerative Diseases (14 papers), Cleft Lip and Palate Research (12 papers), Fetal and Pediatric Neurological Disorders (11 papers) and Hedgehog Signaling Pathway Studies (11 papers). The work is most often cited by research in Developmental Biology (232 citations), Genetics (2.5k citations), Genetics (541 citations), Pediatrics, Perinatology and Child Health (720 citations) and Molecular Biology (2.3k citations). M Baraitser has collaborated with scholars based in United Kingdom, Canada and India. Frequent 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. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Journal of Neurology Neurosurgery & Psychiatry, Neuropediatrics and Archives of Disease in Childhood.

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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