Thomas Haaf

19.2k citations
305 papers · 13.7k · 3 hit papers · h-index 59

Impact in

  • Genetics top 0.1%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Syndromes and Imprinting

Papers in

    • Epigenetics and DNA Methylation 79
    • Genomics and Chromatin Dynamics 48
    • DNA Repair Mechanisms 28
    • Genomic variations and chromosomal abnormalities 49
    • Genetic Syndromes and Imprinting 42
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 26

Thomas Haaf

292 papers receiving 13.2k citations

Thomas Haaf's Hit Papers

A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipes 2002 · 719 citations
7190+8+17Years since publication2505007501000

Peers

Thomas Haaf
Comparison fields: 5 of 153
  • Genetics 5.3k
  • Reproductive Medicine 1.1k
  • Molecular Biology 8.4k
  • Pediatrics, Perinatology and Child Health 2.1k
  • Sensory Systems 485
Replace Heiner Westphal with:
Heiner Westphal United States
Terry Magnuson United States
Patrick Tam Australia
Wei Yan United States
Hans‐Hilger Ropers Germany
Mary F. Lyon United Kingdom
Andrée Dierich France
Yoichi Matsuda Japan
Marianne LeMeur France
Robin Lovell‐Badge United Kingdom
Thomas Haaf relative to Heiner Westphal United States Heiner Westphal's profile →
Citations per field
00.5×1.5×2.4×
Heiner Westphal · 1×
Citations per year

Countries citing papers authored by Thomas Haaf

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Thomas Haaf Line = papers co-authored together Thomas Haaf links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 305 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Demethylation of the zygotic paternal genome
Hit paper breakdown →
20001107
2
Epigenetic reprogramming in mouse primordial germ cells
Hit paper breakdown →
2002981
3
A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipes
Hit paper breakdown →
2002719
4 1995497
5 2006417
6 1999294
7
Elevated levels of Rad51 recombination protein in tumor cells.
2002228
8 2012211
9 2002206
10 1992172
11 1998169
12 2000155
13 1995153
14 2013152
15 2014152
16 1996152
17 1996143
18 2001136
19 2000135
20 2002123

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 305 papers that have together received 13.7k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (80 papers), Epigenetics and DNA Methylation (79 papers), Genomic variations and chromosomal abnormalities (49 papers), Genomics and Chromatin Dynamics (48 papers), Genetic Syndromes and Imprinting (42 papers), Prenatal Screening and Diagnostics (33 papers), DNA Repair Mechanisms (28 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (26 papers). The work is most often cited by research in Genetics (5.3k citations), Reproductive Medicine (1.1k citations), Molecular Biology (8.4k citations), Pediatrics, Perinatology and Child Health (2.1k citations) and Sensory Systems (485 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, Reinald Fundele, Wolfgang Mayer, Ulrich Zechner, Alain Niveleau and Indrajit Nanda. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, Chromosoma, Genomics and Aging.

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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