K Méhes
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Developmental Biology top 5%
Papers in
- Genetics 38
- Genomic variations and chromosomal abnormalities 18
- Co-authors
- P. KajtárNora ShannonAlexandre IrrthumJohn TolmieAlberto PlajaNazneen RahmanAlexa KiddJohn Swansbury
- Journals
- Human Genetics (5 papers)Clinical Genetics (4 papers)The Journal of Pediatrics (3 papers)Journal of Pediatric Gastroenterology and Nutrition (3 papers)European Journal of Pediatrics (3 papers)
- Partner nations
- HungaryUnited KingdomUnited States
In The Last Decade
K Méhes
101 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 95
- Genetics 717
- Developmental Biology 49
- Pediatrics, Perinatology and Child Health 408
- Cell Biology 321
- Molecular Biology 828
Countries citing papers authored by K Méhes
This map shows the geographic impact of K Méhes'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 K Méhes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K Méhes more than expected).
Fields of papers citing papers by K Méhes
This network shows the impact of papers produced by K Méhes. 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 K Méhes. The network helps show where K Méhes may publish in the future.
Co-authors
The 25 scholars most cited alongside K Méhes, 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 | 2005 | 3 | |
| 2 | 2004 | 24 | |
| 3 | 2003 | 2 | |
| 4 | 2002 | 1 | |
| 5 | 2002 | 9 | |
| 6 | 2000 | 16 | |
| 7 | 1999 | 1 | |
| 8 | [Genetic evaluation of mental retardation]. | 1998 | 0 |
| 9 | 1998 | 2 | |
| 10 | 1996 | 16 | |
| 11 | 1995 | 216 | |
| 12 | 1995 | 6 | |
| 13 | 1991 | 5 | |
| 14 | 1988 | 14 | |
| 15 | 1988 | 11 | |
| 16 | Non-random centromere division: analysis of G-banded human chromosomes. | 1981 | 10 |
| 17 | 1980 | 10 | |
| 18 | [Screening of newborn infants for congenital malformations and genetic aberrations]. | 1977 | 1 |
| 19 | 1971 | 1 | |
| 20 | 1969 | 2 |
About K Méhes
K Méhes is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Urology, having authored 105 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Congenital Anomalies and Fetal Surgery (13 papers), Chromosomal and Genetic Variations (11 papers), Prenatal Screening and Diagnostics (10 papers), Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (6 papers), Cancer and Skin Lesions (5 papers) and Birth, Development, and Health (5 papers). The work is most often cited by research in Genetics (717 citations), Developmental Biology (49 citations), Pediatrics, Perinatology and Child Health (408 citations), Cell Biology (321 citations) and Molecular Biology (828 citations). K Méhes has collaborated with scholars based in Hungary, United Kingdom and United States. Frequent co-authors include P. Kajtár, Nora Shannon, Alexandre Irrthum, John Tolmie, Alberto Plaja, Nazneen Rahman, Alexa Kidd, John Swansbury, Sarah Reid and David Fitzpatrick. Their work appears in journals such as Human Genetics, Clinical Genetics, The Journal of Pediatrics, Journal of Pediatric Gastroenterology and Nutrition and European Journal of Pediatrics.
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.