Anneke B. Oostra

4.3k citations

37 papers · 2.9k indexed · h-index 25

Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment 14
Molecular Biology top 2%
- DNA Repair Mechanisms 29
- Genomics and Chromatin Dynamics 12
- CRISPR and Genetic Engineering 6
- Mitochondrial Function and Pathology 3
Cell Biology top 5%
- Microtubule and mitosis dynamics 10
Genetics top 5%
Oncology top 10%
- Cancer-related Molecular Pathways 6
Public Health, Environmental and Occupational Health
- Acute Lymphoblastic Leukemia research 3

Co-authors: Hans Joenje Johan P. de Winter Martin A. Rooimans Fré Arwert Quinten Waisfisz Maureen E. Hoatlin Jûrgen Steltenpool Henri J. van de Vrugt
Cited by: Cancer Research Molecular Biology Cell Biology
Journals: Nature (1 paper)Nucleic Acids Research (1 paper)Nature Communications (2 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Anneke B. Oostra

37 papers receiving 2.9k citations

Peers

Countries citing papers authored by Anneke B. Oostra

Since Specialization

Citations

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

Fields of papers citing papers by Anneke B. Oostra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anneke B. Oostra. 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 Anneke B. Oostra. The network helps show where Anneke B. Oostra may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation Sapientia (Algarve University) ·Sara Carvalhal,Ingrid Bader,Martin A. Rooimans,Anneke B. Oostra,Jesper A. Balk,René G. Feichtinger,Christine Beichler,Michael R. Speicher,Johanna M. van Hagen,Quinten Waisfisz,Mieke M. van Haelst,Martijn Bruijn,Alexandra Tavares,Johannes A. Mayr,Rob M.F. Wolthuis,Raquel A. Oliveira,Job de Lange	2022	15
2	Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2 PLoS ONE ·Atiq Faramarz,Jesper A. Balk,Janne J. M. van Schie,Anneke B. Oostra,Cherien A. Ghandour,Martin A. Rooimans,Rob M.F. Wolthuis,Job de Lange	2020	13
3	Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion Nature Communications ·Janne J. M. van Schie,Atiq Faramarz,Jesper A. Balk,Grant S. Stewart,Erika Cantelli,Anneke B. Oostra,Martin A. Rooimans,Joanna L. Parish,Cynthia de Almeida Estéves,Katja Dumić,Ingeborg Barišić,Karin E. M. Diderich,Marjon A. van Slegtenhorst,Mohammad Mahtab,Francesca M. Pisani,Hein te Riele,Najim Ameziane,Rob M.F. Wolthuis,Job de Lange	2020	35
4	HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair Nucleic Acids Research ·Koichi Sato,Inger Brandsma,Sari E. van Rossum-Fikkert,Nicole S. Verkaik,Anneke B. Oostra,Josephine C. Dorsman,Dik C. van Gent,Puck Knipscheer,Roland Kanaar,Alex N. Zelensky	2019	20
5	Defects in the Fanconi Anemia Pathway and Chromatid Cohesion in Head and Neck Cancer Cancer Research ·Chantal Stoepker,Najim Ameziane,Petra van der Lelij,Irsan Kooi,Anneke B. Oostra,Martin A. Rooimans,Saskia E. van Mil,Arjen Brink,Ralf Dietrich,Jesper A. Balk,Bauke Ylstra,Hans Joenje,Stephan M. Feller,Ruud H. Brakenhoff	2015	25
6	Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function Nature Communications ·Job de Lange,Atiq Faramarz,Anneke B. Oostra,Renée X. de Menezes,Ida H. van der Meulen,Martin A. Rooimans,Davy Rockx,Ruud H. Brakenhoff,Victor W. van Beusechem,Randall W. King,Johan P. de Winter,Rob M.F. Wolthuis	2015	40
7	The iron-sulfur cluster assembly network component NARFL is a key element in the cellular defense against oxidative stress Free Radical Biology and Medicine ·Monique V. Corbin,Davy Rockx,Anneke B. Oostra,Hans Joenje,Josephine C. Dorsman	2015	7
8	A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ubiquitination to the Fanconi Anemia DNA Repair Network Molecular Cell ·Zhijiang Yan,Rong Guo,Manikandan Paramasivam,Weiping Shen,Ling Chen,David Fox,Yucai Wang,Anneke B. Oostra,Julia Kuehl,Duck-Yeon Lee,Minoru Takata,Maureen E. Hoatlin,Detlev Schindler,Hans Joenje,Johan P. de Winter,Lei Li,Michael M. Seidman,Weidong Wang	2012	58
9	Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg DNA repair ·Henri J. van de Vrugt,Mireille Koomen,Sietske T. Bakker,Mariska A. D. Berns,Ngan Ching Cheng,Martin A. van der Valk,Yne de Vries,Martin A. Rooimans,Anneke B. Oostra,Maureen E. Hoatlin,Hein te Riele,Hans Joenje,Fré Arwert	2011	7
10	SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype Nature Genetics ·Chantal Stoepker,Karolina Hain,Beatrice Schuster,Yvonne Hilhorst‐Hofstee,Martin A. Rooimans,Jûrgen Steltenpool,Anneke B. Oostra,Katharina Eirich,Elisabeth T Korthof,Aggie Nieuwint,Nicolaas G.J. Jaspers,Thomas Bettecken,Hans Joenje,Detlev Schindler,John Rouse,Johan P. de Winter	2011	233
11	Fancf‐deficient mice are prone to develop ovarian tumours The Journal of Pathology ·Sietske T. Bakker,Henri J. van de Vrugt,Jenny A. Visser,Elly Delzenne‐Goette,Anja van der Wal,Mariska A. D. Berns,Marieke van de Ven,Anneke B. Oostra,Sandra de Vries,Piet Kramer,Fré Arwert,Martin van der Valk,Johan P. de Winter,Hein te Riele	2011	29
12	Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1 The American Journal of Human Genetics ·Petra van der Lelij,Krystyńa Chrzańowska,Barbara C. Godthelp,Martin A. Rooimans,Anneke B. Oostra,Markus Stümm,Małgorzata Z. Zdzienicka,Hans Joenje,Johan P. de Winter	2010	169
13	Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M Human Molecular Genetics ·Sietske T. Bakker,Henri J. van de Vrugt,Martin A. Rooimans,Anneke B. Oostra,Jûrgen Steltenpool,Elly Delzenne‐Goette,Anja van der Wal,Martin van der Valk,Hans Joenje,Hein te Riele,Johan P. de Winter	2009	108
14	The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2 PLoS ONE ·Petra van der Lelij,Barbara C. Godthelp,Wouter van Zon,Djoke van Gosliga,Anneke B. Oostra,Jûrgen Steltenpool,Jan de Groot,Rik J. Scheper,Rob M.F. Wolthuis,Quinten Waisfisz,F. Darroudi,Hans Joenje,Johan P. de Winter	2009	59
15	FAAP100 is essential for activation of the Fanconi anemia‐associated DNA damage response pathway The EMBO Journal ·Ling Chen,Masamichi Ishiai,Abdullah Mahmood Ali,Annette L. Medhurst,Kornelia Neveling,Reinhard Kalb,Zhijiang Yan,Yutong Xue,Anneke B. Oostra,Arleen D. Auerbach,Maureen E. Hoatlin,Detlev Schindler,Hans Joenje,Johan P. de Winter,Minoru Takata,Amom Ruhikanta Meetei,Weidong Wang	2007	120
16	A case report of a patient with microcephaly, facial dysmorphism, mitomycin-c-sensitive lymphocytes, and susceptibility to lymphoma Cancer Genetics and Cytogenetics ·Sameer Bakhshi,Hans Joenje,Detlev Schindler,Anneke B. Oostra,Anwar N. Mohamed,David N. Madgy,Yaddanapudi Ravindranath,Esteban Abella	2006	16
17	Fanconi Anemia Archives of Otolaryngology - Head and Neck Surgery ·Blanche P. Alter,Hans Joenje,Anneke B. Oostra,Gerard Pals	2005	43
18	Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes Blood ·Marieke Levitus,Martin A. Rooimans,Jûrgen Steltenpool,Nicolle F. C. Cool,Anneke B. Oostra,Christopher G. Mathew,Maureen E. Hoatlin,Quinten Waisfisz,Fré Arwert,Johan P. de Winter,Hans Joenje	2003	177
19	Evidence for at Least Eight Fanconi Anemia Genes The American Journal of Human Genetics ·Hans Joenje,Anneke B. Oostra,Mario Wijker,Franca M. di Summa,Carola G.M. van Berkel,Martin A. Rooimans,Wolfram Ebell,Margreet van Weel,Jan C. Pronk,Manuel Buchwald,Fré Arwert	1997	238
20	Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance. PubMed ·Jerome R. Lo Ten Foe,M. L. Kwee,Martin A. Rooimans,Anneke B. Oostra,A. Veerman,M. van Weel,Richard M. Pauli,N. T. Shahidi,Inderjeet Dokal,Irene Roberts,Çiğdem Altay,Éliane Gluckman,Rachel A. Gibson,Christopher G. Mathew,F. Arwert,Hans Joenje	1997	149

About Anneke B. Oostra

Anneke B. Oostra is a scholar working on Cancer Research, Cell Biology and Molecular Biology, having authored 37 papers that have together received 2.9k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (29 papers), Carcinogens and Genotoxicity Assessment (14 papers), Genomics and Chromatin Dynamics (12 papers), Microtubule and mitosis dynamics (10 papers), CRISPR and Genetic Engineering (6 papers), Cancer-related Molecular Pathways (6 papers), Mitochondrial Function and Pathology (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). The work is most often cited by research in Cancer Research (768 citations), Molecular Biology (2.6k citations) and Cell Biology (393 citations). Anneke B. Oostra has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Hans Joenje, Johan P. de Winter, Martin A. Rooimans, Fré Arwert, Quinten Waisfisz, Maureen E. Hoatlin, Jûrgen Steltenpool, Henri J. van de Vrugt, Aldur W. Eriksson and Zhijiang Yan. Their work appears in journals such as Nature, Nucleic Acids Research and Nature Communications.

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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