World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
53
Citations
11564
World Ranking
3723
National Ranking
132

Roland P. Kuiper publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Roland P. Kuiper sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 157 publications — 33rd percentile

33% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Roland P. Kuiper D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Roland P. Kuiper sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 53 D-Index — 16th percentile

16% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Roland P. Kuiper is affiliated with the Princess Máxima Center in the Netherlands and has an extensive body of research focused on multiple aspects of pediatric oncology, cancer genomics, and molecular biology. They contribute to a range of topics spanning medicine, biochemistry, genetics, and molecular biology, with significant emphasis on acute lymphoblastic leukemia and cancer genomics.

Their recent publications cover various areas in pediatric cancer and genetic predispositions to tumors. Key papers include:

  • Mutational Landscape and Patterns of Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia, 2020, Blood Cancer Discovery
  • Germline MBD4 deficiency causes a multi-tumor predisposition syndrome, 2022, The American Journal of Human Genetics
  • Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience, 2020, Cancer
  • Implementation of paediatric precision oncology into clinical practice: The Individualized Therapies for Children with cancer program 'iTHER', 2022, European Journal of Cancer
  • Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors, 2021, The Journal of Pathology

Collaboration is a significant element of their research career. Frequent co-authors include:

  • Marjolijn C.J. Jongmans (33 publications)
  • Edwin Sonneveld (17 publications)
  • Frank N. van Leeuwen (15 publications)
  • Lennart Kester (14 publications)
  • Jan Loeffen (14 publications)

Roland P. Kuiper has published extensively in several scientific journals. Frequent publication venues include:

  • Blood (10 publications)
  • HemaSphere (6 publications)
  • Haematologica (6 publications)
  • Clinical Cancer Research (4 publications)
  • bioRxiv (Cold Spring Harbor Laboratory) (4 publications)

Their research spans broad fields of study, primarily Medicine and Biochemistry, Genetics and Molecular Biology. More specific subfields include Molecular Biology, Public Health, Environmental and Occupational Health, Genetics, Pathology and Forensic Medicine, and Cancer Research.

Main topics addressed in their work are:

  • Acute Lymphoblastic Leukemia research
  • Cancer Genomics and Diagnostics
  • Genetic factors in colorectal cancer
  • DNA Repair Mechanisms
  • Renal and related cancers
  • Acute Myeloid Leukemia Research
  • Lymphoma Diagnosis and Treatment

Best Publications

  • Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

    Gorica Nikoloski;Saskia M C Langemeijer;Roland P Kuiper;Ruth Knops

  • Acquired mutations in TET2 are common in myelodysplastic syndromes

    Saskia M C Langemeijer;Roland P Kuiper;Marieke Berends;Ruth Knops

  • Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

    Marjolijn J L Ligtenberg;Roland P Kuiper;Tsun Leung Chan;Tsun Leung Chan;Monique Goossens

  • High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression.

    R.P. Kuiper;E.F.P.M. Schoenmakers;S.V. van Reijmersdal;J.Y. Hehir-Kwa

  • Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer.

    Jarno Drost;Ruben van Boxtel;Francis Blokzijl;Tomohiro Mizutani

  • A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer

    Robbert D A Weren;Marjolijn J L Ligtenberg;C Marleen Kets;Richarda M de Voer

  • A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia

    Sohela Shah;Kasmintan A. Schrader;Esmé Waanders;Andrew E. Timms

  • Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

    Marlies J E Kempers;Roland P Kuiper;Charlotte W Ockeloen;Pierre O Chappuis

  • IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL.

    R.P. Kuiper;E. Waanders;V.H. van der Velden;S.V. van Reijmersdal

  • Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL.

    Arian van der Veer;Esmé Waanders;Rob Pieters;Marieke E. Willemse

  • High-resolution DNA copy number and gene expression analyses distinguish chromophobe renal cell carcinomas and renal oncocytomas.

    Maria V Yusenko;Roland P Kuiper;Tamas Boethe;Börje Ljungberg

  • Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitution

    Roland P. Kuiper;Marga Schepens;José Thijssen;Martien van Asseldonk

  • Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome

    Roland P. Kuiper;Lisenka E. L. M. Vissers;Ramprasath Venkatachalam;Danielle Bodmer

  • Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma

    Jennifer M. Kalish;Leslie Doros;Lee J. Helman;Raoul C. Hennekam

  • Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation

    Marjolijn C J Jongmans;Ineke van der Burgt;Peter M Hoogerbrugge;Kees Noordam

  • Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia.

    E. Waanders;V.H. van der Velden;C.E. van der Schoot;F.N. van Leeuwen

  • Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

    Judith E. Grolleman;Richarda M. de Voer;Fadwa A. Elsayed;Maartje Nielsen

  • Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool

    Marjolijn C.J. Jongmans;Jan L.C.M. Loeffen;Esmé Waanders;Peter M. Hoogerbrugge

  • EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients.

    Marjolijn J. L. Ligtenberg;Roland P. Kuiper;Ad Geurts van Kessel;Nicoline Hoogerbrugge

  • Integration of genetic and clinical risk factors improves prognostication in relapsed childhood B-cell precursor acute lymphoblastic leukemia

    Julie A. E. Irving;Amir Enshaei;Catriona A. Parker;Catriona A. Parker;Rosemary Sutton

Frequent Co-Authors

Ad Geurts van Kessel
Ad Geurts van Kessel Radboud University
Rob Pieters
Rob Pieters Princess Máxima Center
Jayne Y. Hehir-Kwa
Jayne Y. Hehir-Kwa Radboud University
Alexander Hoischen
Alexander Hoischen Radboud University
Anthony V. Moorman
Anthony V. Moorman Newcastle University
Iris D. Nagtegaal
Iris D. Nagtegaal Radboud University
Christian Gilissen
Christian Gilissen Radboud University
Jacques J.M. van Dongen
Jacques J.M. van Dongen Leiden University Medical Center
Ian Tomlinson
Ian Tomlinson University of Oxford
Christine J. Harrison
Christine J. Harrison Newcastle University

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