Gerard Pals

15.3k citations
210 papers · 9.5k · 3 hit papers · h-index 50

Impact in

  • Genetics top 0.2%
    • Connective tissue disorders research
    • BRCA gene mutations in cancer
    • Carcinogens and Genotoxicity Assessment

Papers in

    • Connective tissue disorders research 71
    • Glycosylation and Glycoproteins Research 23
    • DNA Repair Mechanisms 12

Gerard Pals

206 papers receiving 9.2k citations

Gerard Pals's Hit Papers

Biallelic Inactivation of BRCA2 in Fanconi Anemia 2002 · 860 citations
8600+10+20Years since publication250500750

Peers

Gerard Pals
Comparison fields: 5 of 128
  • Genetics 3.4k
  • Cancer Research 1.2k
  • Reproductive Medicine 531
  • Gastroenterology 334
  • Obstetrics and Gynecology 446
Replace Sverre Heim with:
Sverre Heim Norway
Minetaro Ogawa Japan
Monica Miozzo Italy
Marie-Claire Gübler France
Leslie I. Gold United States
R. S. K. Chaganti United States
Peter Besmer United States
Jeffrey S. Rubin United States
Karen Carver-Moore United States
Carlo Capella Italy
Gerard Pals relative to Sverre Heim Norway Sverre Heim's profile →
Citations per field
00.5×4.3×
Sverre Heim · 1×
Citations per year

Countries citing papers authored by Gerard Pals

Since Specialization
Citations

This map shows the geographic impact of Gerard Pals'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 Gerard Pals with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gerard Pals more than expected).

Fields of papers citing papers by Gerard Pals

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerard Pals. 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 Gerard Pals. The network helps show where Gerard Pals may publish in the future.

Co-authors

The 25 scholars most cited alongside Gerard Pals, 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 Gerard Pals Line = papers co-authored together Gerard Pals links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 210 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Biallelic Inactivation of BRCA2 in Fanconi Anemia
Hit paper breakdown →
2002860
2
Long-term sequelae of Helicobacter pylori gastritis
Hit paper breakdown →
1995623
3
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer
Hit paper breakdown →
2001529
4 1996355
5 2006351
6 2005344
7
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method.
2003247
8 2004230
9 1993180
10 2004155
11 2011144
12 2009142
13 2012137
14 2002128
15 2015126
16 2007126
17 2002117
18 2001106
19 2016104
20 2016102

About Gerard Pals

Gerard Pals is a scholar working on Genetics, Molecular Biology, Surgery, Pulmonary and Respiratory Medicine and Rheumatology, having authored 210 papers that have together received 9.5k indexed citations. Recurring topics across this work include Connective tissue disorders research (71 papers), Helicobacter pylori-related gastroenterology studies (34 papers), Glycosylation and Glycoproteins Research (23 papers), Aortic Disease and Treatment Approaches (14 papers), Aortic aneurysm repair treatments (14 papers), DNA Repair Mechanisms (12 papers), Bone and Dental Protein Studies (12 papers) and Cardiac Valve Diseases and Treatments (12 papers). The work is most often cited by research in Genetics (3.4k citations), Cancer Research (1.2k citations), Reproductive Medicine (531 citations), Gastroenterology (334 citations) and Obstetrics and Gynecology (446 citations). Gerard Pals has collaborated with scholars based in Netherlands, United States and Poland. Frequent co-authors include Hans Joenje, S.G.M. Meuwissen, Ernst J. Kuipers, A. S. Peña, H.P.M. Festen, Martin A. Rooimans, Anne M. Uyterlinde, Quinten Waisfisz, Fred H. Menko and R. Roosendaal. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Clinical Genetics, European Journal of Vascular and Endovascular Surgery and Human Genetics.

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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