Thomas Haaf
Impact in
- Genetics top 0.1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Reproductive Medicine top 0.5%
Papers in
-
- Epigenetics and DNA Methylation 78
- Genomics and Chromatin Dynamics 48
- DNA Repair Mechanisms 27
- Genetics 153
- Genomic variations and chromosomal abnormalities 49
- Genetic Syndromes and Imprinting 41
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 24
- Co-authors
- Michael Schmid (72 shared papers)Jörn Walter (2 shared papers)Nady El Hajj (39 shared papers)David C. Ward (7 shared papers)Efim I. Golub (6 shared papers)Wolfgang Mayer (3 shared papers)Reinald Fundele (4 shared papers)Ulrich Zechner (43 shared papers)
- Journals
- Cytogenetic and Genome Research (41 papers)Human Genetics (16 papers)Chromosoma (13 papers)Genomics (11 papers)Chromosome Research (6 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Thomas Haaf
287 papers receiving 12.6k citations
Thomas Haaf's Hit Papers
Peers
Comparison fields: 5 of 149
- Genetics 4.9k
- Reproductive Medicine 988
- Molecular Biology 7.9k
- Pediatrics, Perinatology and Child Health 1.9k
- Sensory Systems 460
Countries citing papers authored by Thomas Haaf
This map shows the geographic impact of Thomas Haaf'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 Thomas Haaf with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Haaf more than expected).
Fields of papers citing papers by Thomas Haaf
This network shows the impact of papers produced by Thomas Haaf. 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 Thomas Haaf. The network helps show where Thomas Haaf may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Haaf, 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 299 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Demethylation of the zygotic paternal genome Hit paper breakdown → | 2000 | 1030 |
| 2 | Epigenetic reprogramming in mouse primordial germ cells Hit paper breakdown → | 2002 | 894 |
| 3 | A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipes Hit paper breakdown → | 2002 | 677 |
| 4 | 1995 | 479 | |
| 5 | 2006 | 380 | |
| 6 | 1999 | 286 | |
| 7 | Elevated levels of Rad51 recombination protein in tumor cells. | 2002 | 223 |
| 8 | 2012 | 197 | |
| 9 | 2002 | 194 | |
| 10 | 1992 | 165 | |
| 11 | 1998 | 159 | |
| 12 | 1995 | 150 | |
| 13 | 2000 | 148 | |
| 14 | 2013 | 145 | |
| 15 | 1996 | 141 | |
| 16 | 2014 | 140 | |
| 17 | 1996 | 139 | |
| 18 | 2001 | 130 | |
| 19 | 2000 | 129 | |
| 20 | 2002 | 117 |
About Thomas Haaf
Thomas Haaf is a scholar working on Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 299 papers that have together received 12.9k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (79 papers), Epigenetics and DNA Methylation (78 papers), Genomic variations and chromosomal abnormalities (49 papers), Genomics and Chromatin Dynamics (48 papers), Genetic Syndromes and Imprinting (41 papers), Prenatal Screening and Diagnostics (32 papers), DNA Repair Mechanisms (27 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers). The work is most often cited by research in Genetics (4.9k citations), Reproductive Medicine (988 citations), Molecular Biology (7.9k citations), Pediatrics, Perinatology and Child Health (1.9k citations) and Sensory Systems (460 citations). Thomas Haaf has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Michael Schmid, Jörn Walter, Nady El Hajj, David C. Ward, Efim I. Golub, Wolfgang Mayer, Reinald Fundele, Ulrich Zechner, Alain Niveleau and Indrajit Nanda. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, Chromosoma, Genomics and Chromosome Research.
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.