Martin Bobrow
Impact in
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
- Chronic Lymphocytic Leukemia Research
- Molecular Biology top 1%
- Muscle Physiology and Disorders
Papers in
- Genetics 84
- Genomic variations and chromosomal abnormalities 21
- BRCA gene mutations in cancer 16
- Genetics and Neurodevelopmental Disorders 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
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- Prenatal Screening and Diagnostics 26
- Co-authors
- P. PearsonRoland G. RobertsTheresa M. MarteauDavid BentleyK. MadanStephen AbbsDavid VetrieFrances Flinter
- Journals
- Journal of Medical Genetics (40 papers)Cytogenetic and Genome Research (17 papers)Genomics (16 papers)Nature (13 papers)The Lancet (12 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Martin Bobrow
228 papers receiving 10.2k citations
Hit Papers
Peers
Comparison fields: 5 of 173
- Genetics 4.3k
- Genetics 1.3k
- Molecular Biology 5.3k
- Pediatrics, Perinatology and Child Health 1.3k
- Immunology 1.4k
Countries citing papers authored by Martin Bobrow
This map shows the geographic impact of Martin Bobrow'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 Martin Bobrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martin Bobrow more than expected).
Fields of papers citing papers by Martin Bobrow
This network shows the impact of papers produced by Martin Bobrow. 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 Martin Bobrow. The network helps show where Martin Bobrow may publish in the future.
Co-authors
The 25 scholars most cited alongside Martin Bobrow, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | RESEARCH ETHICS. Ethics review for international data-intensive research | 2016 | 7 |
| 2 | Numbers or words? A randomised controlled trial of presenting screen negative results to pregnant women | 2000 | 2 |
| 3 | 2000 | 17 | |
| 4 | 1994 | 25 | |
| 5 | 1993 | 1 | |
| 6 | 1993 | 21 | |
| 7 | 1992 | 1 | |
| 8 | 1991 | 1 | |
| 9 | Linkage analysis using nine dna polymorphisms along the length of the x chromosome locates the gene for emery dreifuss muscular dystrophy to distal xq | 1986 | 3 |
| 10 | 1984 | 39 | |
| 11 | 1983 | 8 | |
| 12 | 1978 | 3 | |
| 13 | 1978 | 53 | |
| 14 | 1978 | 5 | |
| 15 | EVIDENCE FOR ASSIGNMENT OF LOCI AK1, AK3 AND ACONS TO CHROMOSOME 9 IN MAN | 1976 | 2 |
| 16 | 1976 | 10 | |
| 17 | BETA-2-MICROGLOBULIN GENE IS ON CHROMOSOME-15 AND NOT IN HL-A REGION | 1975 | 2 |
| 18 | Linkage relationships of the HL-A system and beta 2 microglobulin. | 1975 | 1 |
| 19 | 1975 | 9 | |
| 20 | 1970 | 72 |
About Martin Bobrow
Martin Bobrow is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Immunology and Allergy and Genetics, having authored 231 papers that have together received 10.9k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (38 papers), Prenatal Screening and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (21 papers), Chromosomal and Genetic Variations (17 papers), BRCA gene mutations in cancer (16 papers), Genetics and Neurodevelopmental Disorders (12 papers), RNA Research and Splicing (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers). The work is most often cited by research in Genetics (4.3k citations), Genetics (1.3k citations), Molecular Biology (5.3k citations), Pediatrics, Perinatology and Child Health (1.3k citations) and Immunology (1.4k citations). Martin Bobrow has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include P. Pearson, Roland G. Roberts, Theresa M. Marteau, David Bentley, K. Madan, Stephen Abbs, David Vetrie, Frances Flinter, Canio G. Vosa and D. R. Bentley. Their work appears in journals such as Journal of Medical Genetics, Cytogenetic and Genome Research, Genomics, Nature and The Lancet.
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.