M Baraitser

7.8k citations
212 papers · 5.7k · h-index 39

Impact in

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

Papers in

    • Connective tissue disorders research 22
    • Neurogenetic and Muscular Disorders Research 20
    • Craniofacial Disorders and Treatments 17
    • Cleft Lip and Palate Research 12
    • Genetics and Neurodevelopmental Disorders 11

M Baraitser

202 papers receiving 5.3k citations

Peers

M Baraitser
Comparison fields: 5 of 138
  • Developmental Biology 234
  • Genetics 2.7k
  • Genetics 613
  • Pediatrics, Perinatology and Child Health 724
  • Molecular Biology 2.3k
Replace Dian Donnai with:
Dian Donnai United Kingdom
John M. Optiz United States
Alain Verloès France
J. P. Fryns Belgium
Frank Greenberg United States
Roberta A Pagon United States
Jacques L. Michaud Canada
Michel Vekemans France
Ben C.J. Hamel Netherlands
William Reardon United Kingdom
M Baraitser relative to Dian Donnai United Kingdom Dian Donnai's profile →
Citations per field
00.5×1.5×
Dian Donnai · 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 212 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1995375
2 1990262
3 1992229
4 1982193
5 1982158
6 1980103
7 1988103
8 198798
9 199089
10 198882
11 198475
12 197772
13 198772
14 197572
15 198272
16 198064
17 199362
18 198862
19 198961
20 199058

About M Baraitser

M Baraitser is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Developmental Biology, having authored 212 papers that have together received 5.7k indexed citations. Recurring topics across this work include Connective tissue disorders research (22 papers), Neurogenetic and Muscular Disorders Research (20 papers), Congenital limb and hand anomalies (18 papers), Craniofacial Disorders and Treatments (17 papers), Genetic Neurodegenerative Diseases (14 papers), Fetal and Pediatric Neurological Disorders (12 papers), Cleft Lip and Palate Research (12 papers) and Genetics and Neurodevelopmental Disorders (11 papers). The work is most often cited by research in Developmental Biology (234 citations), Genetics (2.7k citations), Genetics (613 citations), Pediatrics, Perinatology and Child Health (724 citations) and Molecular Biology (2.3k citations). M Baraitser has collaborated with scholars based in United Kingdom, India and Canada. Frequent co-authors include R M Winter, Jorge Saraiva, Jane A. Hurst, John Burn, William Reardon, M A Patton, Robin M. Winter, I. Karen Temple, 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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