Daniël Olde Weghuis

1.0k citations

20 papers · 744 indexed · h-index 15

Co-authors: Dominique Smeets Øystein Fodstad Ola Myklebost Ad Geurts van Kessel Anne Forus Marian Stevens‐Kroef Hans Clevers Wouter Korver
Topics: Genomic variations and chromosomal abnormalities (6 papers)Prenatal Screening and Diagnostics (4 papers)Cancer Genomics and Diagnostics (4 papers)
Cited by: Cancer Research Hematology Genetics
Journals: The American Journal of Human Genetics Gene Genomics
Partner nations: Netherlands United States Norway

In The Last Decade

Daniël Olde Weghuis

20 papers receiving 735 citations

Peers

Countries citing papers authored by Daniël Olde Weghuis

Since Specialization

Citations

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

Fields of papers citing papers by Daniël Olde Weghuis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniël Olde Weghuis. 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 Daniël Olde Weghuis. The network helps show where Daniël Olde Weghuis may publish in the future.

Co-authorship network of co-authors of Daniël Olde Weghuis

This figure shows the co-authorship network connecting the top 25 collaborators of Daniël Olde Weghuis. A scholar is included among the top collaborators of Daniël Olde Weghuis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Daniël Olde Weghuis. Daniël Olde Weghuis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A framework for the clinical implementation of optical genome mapping in hematologic malignancies 2024 ·American Journal of Hematology ·Brynn Levy,Rashmi Kanagal‐Shamanna,Nikhil Sahajpal,Kornelia Neveling,Katrina Rack,Barbara Dewaele,Daniël Olde Weghuis,Marian Stevens‐Kroef,Anna Puiggros,Mar Mallo,Ben Clifford,Tuomo Mantere,Alexander Hoischen,Blanca Espinet,Ravindra Kolhe,Françesc Solé,Gordana Raca,Adam C. Smith	19
2	Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping 2021 ·The American Journal of Human Genetics ·Kornelia Neveling,Tuomo Mantere,(unknown),Michiel Oorsprong,Ronald van Beek,Ellen Kater‐Baats,Marc Pauper,(unknown),Dominique Smeets,Daniël Olde Weghuis,Marian Stevens‐Kroef,Alexander Hoischen	110
3	t(15;17)(q24;q21) PML/RARA 2018 ·Atlas of Genetics and Cytogenetics in Oncology and Haematology ·Pino J. Poddighe,Daniël Olde Weghuis	1
4	Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trial 2017 ·Genes Chromosomes and Cancer ·Marian Stevens‐Kroef,Daniël Olde Weghuis,(unknown),Bert van der Reijden,Eline M.P. Cremers,Canan Alhan,Theresia M. Westers,Heleen Visser-Wisselaar,Dana Chiţu,Sónia M. P. R. M. Cunha,Edo Vellenga,Saskia K. Klein,Pierre W. Wijermans,Georgine E. de Greef,M Schaafsma,Petra Muus,Gert J. Ossenkoppele,Arjan A. van de Loosdrecht,Joop H. Jansen	13
5	Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling 2014 ·Molecular Cytogenetics ·Marian Stevens‐Kroef,Eva van den Berg,Daniël Olde Weghuis,Ad Geurts van Kessel,Rolph Pfundt,(unknown),(unknown),Trijnie Dijkhuizen,Patricia J.T.A. Groenen,Annet Simons	17
6	High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myeloma 2012 ·Genes Chromosomes and Cancer ·Marian Stevens‐Kroef,Daniël Olde Weghuis,Sandra Croockewit,(unknown),(unknown),(unknown),(unknown),Annet Simons,Ad Geurts van Kessel	20
7	Microarray‐based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia 2011 ·Genes Chromosomes and Cancer ·Annet Simons,Marian Stevens‐Kroef,(unknown),(unknown),Daniël Olde Weghuis,Eva van den Berg,Esmé Waanders,Peter M. Hoogerbrugge,Roland P. Kuiper,Ad Geurts van Kessel	16
8	Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification 2009 ·Cancer Genetics and Cytogenetics ·Marian Stevens‐Kroef,Annet Simons,(unknown),Ton Feuth,Daniël Olde Weghuis,Arjan Buijs,Reinier Raymakers,Ad Geurts van Kessel	22
9	Detection of cryptic subtelomeric imbalances in fetuses with ultrasound abnormalities 2008 ·European Journal of Medical Genetics ·Brigitte H. W. Faas,Willy M. Nillesen,Sascha Vermeer,Daniël Olde Weghuis,Nicole de Leeuw,Arie P.T. Smits,Conny M.A. van Ravenswaaij‐Arts	11
10	Dandy‐Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33) 2007 ·American Journal of Medical Genetics Part A ·Martin Poot,Hester Y. Kroes,(unknown),Marc J. Eleveld,Liesbeth Rooms,Rutger A. J. Nievelstein,Daniël Olde Weghuis,René C. F. M. Vreuls,G. Hageman,R. Frank Kooy,Ron Hochstenbach	31
11	Fine Mapping of the Human Renal Oncocytoma-Associated Translocation (5;11)(q35;q13) Breakpoint 1997 ·Cancer Genetics and Cytogenetics ·Richard J. Sinke,(unknown),Bert Janssen,Daniël Olde Weghuis,Gerard Merkx,Anke van den Berg,Ed Schuuring,(unknown),Bauke M. de Jong,Ad Geurts van Kessel	29
12	Identification of a human heart FABP pseudogene located on chromosome 13 1997 ·Gene ·Clemens Prinsen,Daniël Olde Weghuis,(unknown),Jacques H. Veerkamp	9
13	The HumanTRIDENT/HFH-11/FKHL16Gene: Structure, Localization, and Promoter Characterization 1997 ·Genomics ·Wouter Korver,Jeroen P. Roose,(unknown),Daniël Olde Weghuis,Diederik de Bruijn,Ad Geurts van Kessel,Hans Clevers	103
14	Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene 1995 ·Genomics ·I.F.M. de Coo,(unknown),Hubert J.M. Smeets,(unknown),J A Morgan-Hughes,Daniël Olde Weghuis,(unknown),(unknown)	36
15	Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas 1995 ·Genes Chromosomes and Cancer ·Anne Forus,Daniël Olde Weghuis,Dominique Smeets,Øystein Fodstad,Ola Myklebost,Ad Geurts van Kessel	125
16	Comparative genomic hybridization analysis of human sarcomas: I. Occurrence of genomic imbalances and identification of a novel major amplicon at 1q21–q22 in soft tissue sarcomas 1995 ·Genes Chromosomes and Cancer ·(unknown),Daniël Olde Weghuis,Dominique Smeets,Øystein Fodstad,Ola Myklebost,(unknown)	125
17	Assignment of the Human Protein Tyrosine Phosphatase Epsilon (PTPRE) Gene to Chromosome 10q26 by Fluorescencein SituHybridization 1995 ·Genomics ·Arn M. J. M. van den Maagdenberg,Helma van den Hurk,Daniël Olde Weghuis,Bé Wieringa,Ad Geurts van Kessel,Wiljan Hendriks	1
18	Definition of a new entity of malignant extragonadal germ cell tumors 1995 ·Genes Chromosomes and Cancer ·Jannie van Echten,Bauke M. de Jong,Richard J. Sinke,Daniël Olde Weghuis,Dirk Th. Sleijfer,J. Wolter Oosterhuis	17
19	Fine Mapping of the Human Bone Morphogenetic Protein-4 Gene (BMP4) to Chromosome 14q22-q23 by in Situ Hybridization 1995 ·Genomics ·Arthur van den Wijngaard,Daniël Olde Weghuis,C.J.C. Boersma,E.J.J. van Zoelen,Ad Geurts van Kessel,Wiebe Olijve	21
20	The Mouse Gene Ptprf Encoding the Leukocyte Common Antigen-Related Molecule LAR: Cloning, Characterization, and Chromosomal Localization 1995 ·Genomics ·Roel Q.J. Schaapveld,(unknown),Jan Schepens,Daniël Olde Weghuis,Ad Geurts van Kessel,Bé Wieringa,Wiljan Hendriks	18

About Daniël Olde Weghuis

Daniël Olde Weghuis is a scholar working on Hematology, Genetics and Immunology, having authored 20 papers that have together received 744 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Cancer Genomics and Diagnostics (4 papers). The work is most often cited by research in Cancer Research (174 citations), Hematology (111 citations) and Genetics (238 citations). Daniël Olde Weghuis has collaborated with scholars based in Netherlands, United States and Norway. Frequent co-authors include Dominique Smeets, Øystein Fodstad, Ola Myklebost, Ad Geurts van Kessel, Anne Forus, Marian Stevens‐Kroef, Hans Clevers, Wouter Korver, Diederik de Bruijn and Ad Geurts van Kessel. Their work appears in journals such as The American Journal of Human Genetics, Gene and Genomics.

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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