M.H. Skolnick
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
-
- Genetic factors in colorectal cancer
Papers in
- Genetics 7
- BRCA gene mutations in cancer 5
- Genetic Associations and Epidemiology 4
- Genomic variations and chromosomal abnormalities 2
- Hemoglobinopathies and Related Disorders 2
-
- DNA Repair Mechanisms 1
- Co-authors
- Lisa Cannon‐Albright (6 shared papers)Douglas F. Easton (1 shared paper)David E. Goldgar (2 shared papers)William P. McWhorter (2 shared papers)D. C. Rao (2 shared papers)Alun Thomas (1 shared paper)Cathryn M. Lewis (2 shared papers)D. Timothy Bishop (3 shared papers)
- Journals
- Genetic Epidemiology (4 papers)Blood (2 papers)JNCI Journal of the National Cancer Institute (2 papers)Human Molecular Genetics (1 paper)The Pharmacogenomics Journal (1 paper)
- Partner nations
- United StatesItalyGermany
In The Last Decade
M.H. Skolnick
18 papers receiving 1.4k citations
M.H. Skolnick's Hit Papers
Peers
Comparison fields: 5 of 87
- Genetics 596
- Pathology and Forensic Medicine 334
- Cancer Research 212
- Endocrinology, Diabetes and Metabolism 200
- Oncology 295
Countries citing papers authored by M.H. Skolnick
This map shows the geographic impact of M.H. Skolnick'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.H. Skolnick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M.H. Skolnick more than expected).
Fields of papers citing papers by M.H. Skolnick
This network shows the impact of papers produced by M.H. Skolnick. 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.H. Skolnick. The network helps show where M.H. Skolnick may publish in the future.
Co-authors
The 25 scholars most cited alongside M.H. Skolnick, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands Hit paper breakdown → | 1994 | 817 |
| 2 | Familiality of cancer in Utah. | 1994 | 164 |
| 3 | 1985 | 120 | |
| 4 | 1994 | 84 | |
| 5 | Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM). | 1994 | 66 |
| 6 | 1999 | 61 | |
| 7 | 1988 | 58 | |
| 8 | 2004 | 47 | |
| 9 | 1981 | 34 | |
| 10 | 2002 | 22 | |
| 11 | 1980 | 21 | |
| 12 | 1986 | 13 | |
| 13 | 2001 | 10 | |
| 14 | 1989 | 7 | |
| 15 | 2008 | 5 | |
| 16 | 1981 | 5 | |
| 17 | 2008 | 3 | |
| 18 | 1986 | 2 | |
| 19 | Conference on Methods of Automatic Family Reconstitution : Florence, Italy, April 4-6, 1977 | 1978 | 1 |
| 20 | DNA sequence polymorphism at arbitrary loci. | 1982 | 1 |
About M.H. Skolnick
M.H. Skolnick is a scholar working on Genetics, Molecular Biology, Genetics, Pulmonary and Respiratory Medicine and Artificial Intelligence, having authored 23 papers that have together received 1.5k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genetic Associations and Epidemiology (4 papers), Prostate Cancer Diagnosis and Treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Hemoglobinopathies and Related Disorders (2 papers), Iron Metabolism and Disorders (2 papers), DNA Repair Mechanisms (1 paper) and Cutaneous Melanoma Detection and Management (1 paper). The work is most often cited by research in Genetics (596 citations), Pathology and Forensic Medicine (334 citations), Cancer Research (212 citations), Endocrinology, Diabetes and Metabolism (200 citations) and Oncology (295 citations). M.H. Skolnick has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Lisa Cannon‐Albright, Douglas F. Easton, David E. Goldgar, William P. McWhorter, D. C. Rao, Alun Thomas, Cathryn M. Lewis, D. Timothy Bishop, K.K. Namboodiri and Jeffrey Swensen. Their work appears in journals such as Genetic Epidemiology, Blood, JNCI Journal of the National Cancer Institute, Human Molecular Genetics and The Pharmacogenomics Journal.
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.