Marjan M. Weiss

7.2k citations

87 papers · 2.9k indexed · h-index 29

Co-authors: Gerrit A. Meijer Ernst J. Kuipers Erik A. Sistermans Mario Hermsen Cindy Postma S.G.M. Meuwissen P. J. van Diest Frederik J. Hes
Topics: Genomic variations and chromosomal abnormalities (22 papers)Genetic factors in colorectal cancer (17 papers)Cancer Genomics and Diagnostics (16 papers)
Cited by: Cancer Research Pathology and Forensic Medicine Genetics
Journals: SHILAP Revista de lepidopterologíaGastroenterology Oncogene
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Marjan M. Weiss

86 papers receiving 2.8k citations

Peers

Countries citing papers authored by Marjan M. Weiss

Since Specialization

Citations

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

Fields of papers citing papers by Marjan M. Weiss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marjan M. Weiss. 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 Marjan M. Weiss. The network helps show where Marjan M. Weiss may publish in the future.

Co-authorship network of co-authors of Marjan M. Weiss

This figure shows the co-authorship network connecting the top 25 collaborators of Marjan M. Weiss. A scholar is included among the top collaborators of Marjan M. Weiss 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 Marjan M. Weiss. Marjan M. Weiss 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	Bleeding symptoms in persons with rare bleeding disorders and a heterozygous genotype: data from the Rare Bleeding Disorders in the Netherlands study 2025 ·Journal of Thrombosis and Haemostasis ·Sara M. Willems,Marjon H. Cnossen,Nick van Es,Paul L. den Exter,(unknown),(unknown),Karina Meijer,Laurens Nieuwenhuizen,Sanna R. Rijpma,(unknown),Annet Simons,Roger Schutgens,Marjan M. Weiss,Nicole M. A. Blijlevens,Waander L. van Heerde,Saskia E.M. Schols	1
2	HiFi long-read genomes for difficult-to-detect, clinically relevant variants 2025 ·The American Journal of Human Genetics ·Wolfram Höps,Marjan M. Weiss,Ronny Derks,Jordi Corominas Galbany,(unknown),(unknown),(unknown),(unknown),(unknown),Egor Dolzhenko,Xiao Chen,Arthur van den Wijngaard,Michael A. Eberle,Helger G. Yntema,Alexander Hoischen,Christian Gilissen,Lisenka E.L.M. Vissers	6
3	Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands study 2024 ·Research and Practice in Thrombosis and Haemostasis ·(unknown),Annet Simons,(unknown),Marjan M. Weiss,Sanna R. Rijpma,(unknown),Karina Meijer,Marjon H. Cnossen,Roger E. G. Schutgens,Nick van Es,Laurens Nieuwenhuizen,Paul L. den Exter,(unknown),Nicole M. A. Blijlevens,Waander L. van Heerde,Saskia E.M. Schols	4
4	Early On-treatment Circulating Tumor DNA Measurements and Response to Immune Checkpoint Inhibitors in Advanced Urothelial Cancer 2023 ·European Urology Oncology ·Sofie H. Tolmeijer,Sandra van Wilpe,Maartje J. Geerlings,Daniel von Rhein,Tineke J. Smilde,(unknown),Harm Westdorp,(unknown),Irma M. Oving,(unknown),Antoine G. van der Heijden,Tom Hofste,Marjan M. Weiss,Jack A. Schalken,Winald R. Gerritsen,Marjolijn J. L. Ligtenberg,Niven Mehra	10
5	Fetal fraction of cell-free DNA in noninvasive prenatal testing and adverse pregnancy outcomes: a nationwide retrospective cohort study of 56,110 pregnant women 2023 ·American Journal of Obstetrics and Gynecology ·(unknown),P Scheffer,Jens Henrichs,Caroline J. Bax,Neeltje Crombag,Marjan M. Weiss,Merryn Macville,Diane Van Opstal,Elles M. J. Boon,Erik A. Sistermans,Lidewij Henneman,Ewoud Schuit,Mireille N. Bekker	10
6	Circulating Tumor DNA-Based Disease Monitoring of Patients with Locally Advanced Esophageal Cancer 2022 ·Cancers ·(unknown),Maartje J. Geerlings,Daniel von Rhein,Sofie H. Tolmeijer,Marjan M. Weiss,Christian Gilissen,Tom Hofste,(unknown),Marcel J. R. Janssen,Heidi Rütten,Camiel Rosman,Rachel S. van der Post,Bastiaan Klarenbeek,Marjolijn J. L. Ligtenberg	17
7	A novel CCM2 variant in a family with non‐progressive cognitive complaints and cerebral microbleeds 2016 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Petra E. Cohn‐Hokke,Henne Holstege,Marjan M. Weiss,Wiesje M. van der Flier,Frederik Barkhof,Erik A. Sistermans,Yolande A.L. Pijnenburg,John C. van Swieten,Hanne Meijers‐Heijboer,Philip Scheltens	4
8	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part I—clinical impact 2016 ·Prenatal Diagnosis ·Dick Oepkes,Godelieve C.M.L. Page‐Christiaens,Caroline J. Bax,Mireille N. Bekker,Catia M. Bilardo,Elles M. J. Boon,G. Heleen Schuring‐Blom,A. Coumans,Brigitte H. W. Faas,Robert‐Jan H. Galjaard,Attie T. J. I. Go,Lidewij Henneman,Merryn Macville,Eva Pajkrt,Ron F. Suijkerbuijk,Karin Huijsdens–van Amsterdam,Diane Van Opstal,E. J. T. Verweij,Marjan M. Weiss,Erik A. Sistermans	110
9	Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndrome. 2012 ·PubMed ·Shazia Micheal,Muhammad Imran Khan,Farah Akhtar,Marjan M. Weiss,Farah Islam,(unknown),Raheel Qamar,Alessandra Maugeri,Anneke I. den Hollander	14
10	Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus 2012 ·European Journal of Human Genetics ·Magdaléna Harakaľová,Jasper van der Smagt,Carolien G. F. de Kovel,Ruben van’t Slot,Martin Poot,Isaäc J. Nijman,Jelena Medic,(unknown),Jaap W. Deckers,Jolien W. Roos‐Hesselink,Marja W. Wessels,Hubert F. Baars,Marjan M. Weiss,Gerard Pals,Lisa Golmard,Xavier Jeunemaı̂tre,Dick Lindhout,Edwin Cuppen,Annette F. Baas	32
11	Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy 2010 ·Netherlands Heart Journal ·(unknown),Ronald H. Lekanne Deprez,Marjan M. Weiss,Marjon van Slegtenhorst,Marieke Joosten,Jasper J. van der Smagt,Nicolaas de Jonge,Wilhelmina S. Kerstjens‐Frederikse,(unknown),(unknown),Maarten P. van den Berg,(unknown),J. Peter van Tintelen	10
12	Low penetrance of a SDHB mutation in a large Dutch paraganglioma family 2010 ·BMC Medical Genetics ·Frederik J. Hes,Marjan M. Weiss,(unknown),Noel F.C.C. de Miranda,(unknown),Bert A. Bonsing,Marcel P. M. Stokkel,Hans Morreau,Johannes A. Romijn,Jeroen C. Jansen,A. H. J. T. Vriends,Jean‐Pierre Bayley,Eleonora P.M. Corssmit	38
13	Complete COL1A1 allele deletions in osteogenesis imperfecta 2010 ·Genetics in Medicine ·Fleur S. van Dijk,(unknown),Ariana Kariminejad,Carlo Marcelis,Astrid S. Plomp,Pauline Terhal,Hanne Meijers‐Heijboer,Marjan M. Weiss,Rick R. van Rijn,Jan M. Cobben,Gerard Pals	33
14	Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancer 2010 ·Breast Cancer Research and Treatment ·Marijke Wasielewski,(unknown),(unknown),Maartje Nielsen,Ans van den Ouweland,Carli M.J. Tops,Juul Wijnen,Hans F. A. Vasen,Marjan M. Weiss,Jan G.M. Klijn,Peter Devilee,Frederik J. Hes,Mieke Schutte	39
15	A 400 kb duplication, 2.4 Mb triplication and 130 kb duplication of 9q34.3 in a patient with severe mental retardation 2008 ·European Journal of Medical Genetics ·Antoinet C.J. Gijsbers,Emilia K. Bijlsma,Marjan M. Weiss,Egbert Bakker,Martijn H. Breuning,(unknown),Claudia Ruivenkamp	10
16	Genomic profiling of gastric cancer predicts lymph node status and survival 2003 ·Oncogene ·Marjan M. Weiss,Ernst J. Kuipers,Cindy Postma,Antoine M. Snijders,Ivar Siccama,Daniel Pinkel,Johan Westerga,S.G.M. Meuwissen,Donna G. Albertson,Gerrit A. Meijer	93
17	Comparative Genomic Hybridization in Cancer Investigations 2003 ·Molecular Cytogenetics ·Marjan M. Weiss,Mario Hermsen,Gerrit A. Meijer,Paul J. van Diest	2
18	Quantitative assessment of gastric corpus atrophy in subjects using omeprazole: a randomized follow-up study 2001 ·The American Journal of Gastroenterology ·Nicole C.T. van Grieken,Gerrit A. Meijer,Marjan M. Weiss,Elisabeth Bloemena,J. Lindeman,Jan P. A. Baak,S.G.M. Meuwissen,Ernst J. Kuipers	23
19	Demystified....comparative genomic hybridization 1999 ·Journal of Clinical Pathology ·Marjan M. Weiss,Mario Hermsen,Gerrit A. Meijer,Nicole C.T. van Grieken,J. P. A. Baak,Ernst J. Kuipers,P. J. van Diest	8
20	Demystified . . . Comparative genomic hybridisation 1999 ·Molecular Pathology ·Marjan M. Weiss,Mario Hermsen,Gerrit A. Meijer,Nicole C.T. van Grieken,J. P. A. Baak,Ernst J. Kuipers,P. J. van Diest	5

About Marjan M. Weiss

Marjan M. Weiss is a scholar working on Cancer Research, Genetics and Pathology and Forensic Medicine, having authored 87 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Genetic factors in colorectal cancer (17 papers) and Cancer Genomics and Diagnostics (16 papers). The work is most often cited by research in Cancer Research (737 citations), Pathology and Forensic Medicine (715 citations) and Genetics (992 citations). Marjan M. Weiss has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Gerrit A. Meijer, Ernst J. Kuipers, Erik A. Sistermans, Mario Hermsen, Cindy Postma, S.G.M. Meuwissen, P. J. van Diest, Frederik J. Hes, Nicole C.T. van Grieken and Antoine M. Snijders. Their work appears in journals such as SHILAP Revista de lepidopterología, Gastroenterology and Oncogene.

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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