Robert M.W. Hofstra

23.0k total citations · 2 hit papers
251 papers, 12.9k citations indexed

About

Robert M.W. Hofstra is a scholar working on Molecular Biology, Surgery and Pathology and Forensic Medicine. According to data from OpenAlex, Robert M.W. Hofstra has authored 251 papers receiving a total of 12.9k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Molecular Biology, 76 papers in Surgery and 67 papers in Pathology and Forensic Medicine. Recurrent topics in Robert M.W. Hofstra's work include Genetic factors in colorectal cancer (61 papers), Congenital gastrointestinal and neural anomalies (58 papers) and Cancer Genomics and Diagnostics (36 papers). Robert M.W. Hofstra is often cited by papers focused on Genetic factors in colorectal cancer (61 papers), Congenital gastrointestinal and neural anomalies (58 papers) and Cancer Genomics and Diagnostics (36 papers). Robert M.W. Hofstra collaborates with scholars based in Netherlands, United States and United Kingdom. Robert M.W. Hofstra's co-authors include Charles H.C.M. Buys, Rolf H. Sijmons, Harry Hollema, Jan H. Kleibeuker, Elisabeth G.E. de Vries, Isabella Ceccherini, Rein P. Stulp, John Th. M. Plukker, Gerard J. te Meerman and Thera P. Links and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Robert M.W. Hofstra

249 papers receiving 12.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

1994 872 citations Robert M.W. Hofstra, Isabella Ceccherini et al. profile →
Evidence Based Selection of Housekeeping Genes

2007 611 citations Robert M.W. Hofstra, Elisabeth G.E. de Vries et al. profile →

Peers

Robert M.W. Hofstra

SURGE

PFM

ONCOL

GENET

Catharina Larsson Sweden

Mark Lathrop France

Charles E. Jackson United States

Masahide Takahashi Japan

Shiro Ikegawa Japan

Moosa Mohammadi United States

Finn Cilius Nielsen Denmark

Nazneen Aziz United States

Peter Mündel United States

Allen M. Spiegel United States

Catharina Larsson Sweden

Robert M.W. Hofstra

6.1k ×1.2

2.1k ×0.6

SURGE

1.3k ×0.5

PFM

4.2k ×1.5

ONCOL

2.8k ×1.2

GENET

Citations per year, relative to Robert M.W. Hofstra Robert M.W. Hofstra (= 1×) peers Catharina Larsson

Countries citing papers authored by Robert M.W. Hofstra

Since Specialization

Citations

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

Fields of papers citing papers by Robert M.W. Hofstra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert M.W. Hofstra. 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 Robert M.W. Hofstra. The network helps show where Robert M.W. Hofstra may publish in the future.

Co-authorship network of co-authors of Robert M.W. Hofstra

This figure shows the co-authorship network connecting the top 25 collaborators of Robert M.W. Hofstra. A scholar is included among the top collaborators of Robert M.W. Hofstra 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 Robert M.W. Hofstra. Robert M.W. Hofstra 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

Sacchetti, Andrea, Gerben Schaaf, Eric M. Bindels, et al.. (2023). A combinatorial panel for flow cytometry‐based isolation of enteric nervous system cells from human intestine. EMBO Reports. 24(4). e55789–e55789. 4 indexed citations

Kuil, Laura E., Eric M. Bindels, Robert M.W. Hofstra, et al.. (2023). Unbiased characterization of the larval zebrafish enteric nervous system at a single cell transcriptomic level. iScience. 26(7). 107070–107070. 9 indexed citations

Demirdas, Serwet, Edwin H. Jacobs, Esmée Oussoren, et al.. (2020). Using Out-of-Batch Reference Populations to Improve Untargeted Metabolomics for Screening Inborn Errors of Metabolism. Metabolites. 11(1). 8–8. 12 indexed citations

Akker, Peter C. van den, Anna M.G. Pasmooij, Hans Joenje, et al.. (2018). . Data Archiving and Networked Services (DANS). 10 indexed citations

Goverde, Anne, Marleen Dekker, Marco J. Bruno, et al.. (2017). Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity. PLoS Genetics. 13(5). e1006765–e1006765. 15 indexed citations

Vaes, Nathalie, Marjolein H.F.M. Lentjes, Marion J. Gijbels, et al.. (2017). NDRG 4, an early detection marker for colorectal cancer, is specifically expressed in enteric neurons. Neurogastroenterology & Motility. 29(9). 9 indexed citations

Torroglosa, Ana, Maria M. Alves, Roberto Fernández, et al.. (2016). Epigenetics in ENS development and Hirschsprung disease. Developmental Biology. 417(2). 209–216. 34 indexed citations

Bergman, Jorieke E. H., Nicole Janssen, Almer M. van der Sloot, et al.. (2012). A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome. Human Mutation. 33(8). 1251–1260. 50 indexed citations

Sribudiani, Yunia, Joanne Verheij, Matthew Carroll, et al.. (2012). Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutations. Genetics in Medicine. 15(4). 310–313. 30 indexed citations

10.

Zwaag, Paul A. van der, Maarten P. van den Berg, Moniek G.P.J. Cox, et al.. (2010). One Mutation Fits All: Phospholamban R14del Causes Both Dilated Cardiomyopathy and Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia. Circulation. 122(21). 3 indexed citations

11.

Pinto, Carla, Isabel Veiga, Manuela Pinheiro, et al.. (2009). TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset. Familial Cancer. 8(4). 383–390. 12 indexed citations

12.

Akker, Peter C. van den, et al.. (2009). Design and Validation of a Conformation-Sensitive Capillary Electrophoresis System for Mutation Identification of the COL7A1 Gene with Automated Peak Comparison. Genetic Testing and Molecular Biomarkers. 13(5). 589–597. 3 indexed citations

13.

Crijns, Anne P.G., Pauline de Graeff, Dirk Geerts, et al.. (2007). MEIS and PBX homeobox proteins in ovarian cancer. European Journal of Cancer. 43(17). 2495–2505. 76 indexed citations

14.

Koornstra, Jan J., Mathilde Jalving, Jantine L. Westra, et al.. (2005). Expression of tumour necrosis factor-related apoptosis-inducing ligand death receptors in sporadic and hereditary colorectal tumours: Potential targets for apoptosis induction. European Journal of Cancer. 41(8). 1195–1202. 29 indexed citations

15.

Hofstra, Robert M.W., et al.. (2000). GFR alpha-3 variants in human lung carcinoma.. Data Archiving and Networked Services (DANS). 1 indexed citations

16.

Wu, Yige, et al.. (2000). Germline hMLH3 mutations in patients with suspected HNPCC.. Data Archiving and Networked Services (DANS). 3 indexed citations

17.

Griseri, Paola, Renata Bocciardi, Robert M.W. Hofstra, et al.. (2000). A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease. European Journal of Human Genetics. 8(9). 721–724. 37 indexed citations

18.

Griseri, Paola, Renata Bocciardi, Robert M.W. Hofstra, et al.. (1999). Decreased frequency of a neutral sequence variant of the RET proto-oncogene in sporadic Hirschsprung disease.. Data Archiving and Networked Services (DANS). 1 indexed citations

19.

Wu, Yuanqing, et al.. (1999). A DGGE system for comprehensive mutation screening of the complete coding regions of BRCA1 and BRCA2 outside exons 11. Data Archiving and Networked Services (DANS). 5 indexed citations

20.

Hofstra, Robert M.W., Tineke Stelwagen, & Rein P. Stulp. (1994). RET mutations in MEN 2 associated diseases. The American Journal of Human Genetics. 55. 8 indexed citations

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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