Edwin Verlind

977 citations

28 papers · 690 · h-index 15

Impact in

Pathology and Forensic Medicine top 5%
- Genetic factors in colorectal cancer
Cancer Research
- Cancer Genomics and Diagnostics

Papers in

Molecular Biology 9
- Glycosylation and Glycoproteins Research 2
Genetics 4
- Genomic variations and chromosomal abnormalities 3

Co-authors: Charles H.C.M. Buys (19 shared papers)Robert M.W. Hofstra (10 shared papers)Hans Scheffer (15 shared papers)Rob G.J. Mensink (2 shared papers)Harry Hollema (2 shared papers)Ate G.J. van der Zee (2 shared papers)Maran J.W. Berends (2 shared papers)Jan H. Kleibeuker (2 shared papers)
Journals: Human Genetics (5 papers)Human Mutation (3 papers)European Journal of Human Genetics (2 papers)Genes Chromosomes and Cancer (2 papers)Gastroenterology (1 paper)
Partner nations: Netherlands United States Germany

In The Last Decade

Edwin Verlind

28 papers receiving 662 citations

Peers

Countries citing papers authored by Edwin Verlind

Since Specialization

Citations

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

Fields of papers citing papers by Edwin Verlind

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edwin Verlind. 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 Edwin Verlind. The network helps show where Edwin Verlind may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A role for MLH3 in hereditary nonpolyposis colorectal cancer Nature Genetics ·Ying Wu, Maran J.W. Berends, Rolf H. Sijmons, Rob G.J. Mensink, Edwin Verlind, Krista Kooi, Tineke van der Sluis, Claudia Kempinga, Ate G.J. van der Zee, Harry Hollema, Charles H.C.M. Buys, Jan H. Kleibeuker, Robert M.W. Hofstra	2001	128
2	Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms Gastroenterology ·Ying Wu, Rob G.J. Mensink, Edwin Verlind, Rolf H. Sijmons, Charles H.C.M. Buys, Robert M.W. Hofstra, Maran J.W. Berends, Jan H. Kleibeuker, Jan G. Post, Claudia Kempinga, Tineke van der Sluis, Harry Hollema, Ate G.J. van der Zee	2001	126
3	Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flowchart European Journal of Pediatrics ·Jan Peter Rake, Annelies M. ten Berge, Gepke Visser, Edwin Verlind, Klary E. Niezen‐Koning, Charles H.C.M. Buys, Gerrit Smit, Hans Scheffer	2000	59
4	Three novel KCNA1 mutations in episodic ataxia type I families Human Genetics ·Hans Scheffer, E. R. Brunt, G J J Mol, Pieter van der Vlies, Not Available Not Available, Edwin Verlind, G.W.H. Mantel, Y. N. Averyanov, Robert M.W. Hofstra, C.H.C.M. Buys	1998	51
5	High Frequency of TP53 Mutations in Juvenile Pilocytic Astrocytomas Indicates Role of TP53 in the Development of These Tumors Brain Pathology ·Vanessa M. Hayes, Clemens M.F. Dirven, Anke Dam, Edwin Verlind, Willemina M. Molenaar, Jan Jakob A. Mooij, Robert M.W. Hofstra, Charles H.C.M. Buys	1999	41
6	Exempting Homologous Pseudogene Sequences from Polymerase Chain Reaction Amplification Allows Genomic Keratin 14 Hotspot Mutation Analysis Journal of Investigative Dermatology ·Petra H.L. Hut, Pieter van der Vlies, Edwin Verlind, Charles H.C.M. Buys, Hans Scheffer, Marcel F. Jonkman, Hiroshi Shimizu	2000	32
7	Novel Missense Mutation in the L1 Gene in a Child With Corpus Callosum Agenesis, Retardation, Adducted Thumbs, Spastic Paraparesis, and Hydrocephalus Journal of Child Neurology ·László Sztriha, Philippe Frossard, Robert M.W. Hofstra, Edwin Verlind, Michael Nork	2000	26
8	Comprehensive TP53-Denaturing Gradient Gel Electrophoresis Mutation Detection Assay Also Applicable to Archival Paraffin-Embedded Tissue Diagnostic Molecular Pathology ·Vanessa M. Hayes, Wim Bleeker, Edwin Verlind, Tineke Timmer, Arend Karrenbeld, John Th. M. Plukker, Munro P. Marx, Robert M.W. Hofstra, Charles H.C.M. Buys	1999	25
9	RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia Cancer Genetics and Cytogenetics ·W. J. Van Everdink, Ancha Baranova, Chantal Lummen, T. V. Tyazhelova, Maaike W.G. Looman, Dmitry Ivanov, Edwin Verlind, Anna Pestova, Hette Faber, Anneke Y. van der Veen, N. K. Yankovsky, Edo Vellenga, Charles H.C.M. Buys	2003	21
10	X-linked hydrocephalus: a novel missense mutation in the L1CAM gene Pediatric Neurology ·L.ászló Sztriha, Yvonne J. Vos, Edwin Verlind, J. G. Johansen, Bertel Berg	2002	20
11	Prognostic significance of K- ras and TP53 mutations in the role of adjuvant chemotherapy on survival in patients with dukes C colon cancer Diseases of the Colon & Rectum ·Wim Bleeker, Vanessa M. Hayes, Arend Karrenbeld, Robert M.W. Hofstra, Edwin Verlind, J. Hermans, S Poppema, C.H.C.M. Buys, John Th. M. Plukker	2001	20
12	A Yeast Artificial Chromosome Contig That Spans the RB1-D13S31 Interval on Human Chromosome 13 and Encompasses the Frequently Deleted Region in B-cell Chronic Lymphocytic Leukemia Genomics ·Lesleyann Hawthorn, Terry Roberts, Edwin Verlind, R. Frank Kooy, John K. Cowell	1995	19
13	New comprehensive denaturing-gradient-gel- electrophoresis assay forKRAS mutation detection applied to paraffin-embedded tumours Genes Chromosomes and Cancer ·Vanessa M. Hayes, Jantine L. Westra, Edwin Verlind, Wim Bleeker, John Th. M. Plukker, Robert M.W. Hofstra, Charles H.C.M. Buys	2000	17
14	Occurrence of deletion of a COL2A1 allele as the mutation in Stickler syndrome shows that a collagen type II dosage effect underlies this syndrome Human Mutation ·Annemarie H. van der Hout, Edwin Verlind, Frits A. Beemer, Charles H.C.M. Buys, Robert M.W. Hofstra, Hans Scheffer	2002	16
15	RAPID SCREENING FOR ΔF508 DELETION IN CYSTIC FIBROSIS The Lancet ·George R. Taylor, J S Noble, June Hall, Philip Quirke, A. Stewart, R Mueller, Hans Scheffer, Edwin Verlind, Dirk Penninga, Gerard te Meerman, L.P. Ten Kate, Charles H.C.M. Buys, Christopher G. Mathew, Roland G. Roberts, Ann Harris, D. R. Bentley, Martin Bobrow	1989	15
16	Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosa Human Genetics ·Hans Scheffer, Rein P. Stulp, Edwin Verlind, Merel van der Meulen, Leena Bruckner‐Tuderman, Tobias Gedde‐Dahl, G.J. te Meerman, Arnoud Sonnenberg, Charles H.C.M. Buys, Marcel F. Jonkman	1997	14
17	Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes Human Mutation ·Jan Peter Rake, Annelies M. ten Berge, Gepke Visser, Edwin Verlind, Klary E. Niezen‐Koning, Charles H.C.M. Buys, G. P. A. Smit, Hans Scheffer	2000	10
18	Glycogen storage disease type Ia: Four novel mutations (175delGG, R170X, G266V and V338F) identified Human Mutation ·Jan Peter Rake, Annelies M. ten Berge, Edwin Verlind, Gepke Visser, Klary E. Niezen‐Koning, Charles H.C.M. Buys, Gerrit Smit, Hans Scheffer	1999	10
19	A Deletion Hybrid Breakpoint Mapof the Chromosomal Region13q14-q21 Orders 19 GeneticMarkers in 10 Intervals European Journal of Human Genetics ·R. Frank Kooy, Edwin Verlind, Roderick H.J. Houwen, David N. Shapiro, Lesleyann Hawthorn, John K. Cowell, Hans Scheffer, Charles H.C.M. Buys	1994	7
20	Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13 Human Genetics ·R. Frank Kooy, Anneke Y. van der Veen, Edwin Verlind, Roderick H.J. Houwen, Hans Scheffer, Charles H.C.M. Buys	1993	7

About Edwin Verlind

Edwin Verlind is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Oncology and Cell Biology, having authored 28 papers that have together received 690 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Cystic Fibrosis Research Advances (3 papers), Glycogen Storage Diseases and Myoclonus (3 papers), Glycosylation and Glycoproteins Research (2 papers), Cancer Genomics and Diagnostics (2 papers), Amino Acid Enzymes and Metabolism (2 papers), Cancer-related Molecular Pathways (2 papers) and Axon Guidance and Neuronal Signaling (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (253 citations), Cancer Research (101 citations), Oncology (181 citations), Genetics (56 citations) and Rheumatology (73 citations). Edwin Verlind has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Charles H.C.M. Buys, Robert M.W. Hofstra, Hans Scheffer, Rob G.J. Mensink, Harry Hollema, Ate G.J. van der Zee, Maran J.W. Berends, Jan H. Kleibeuker, Ying Wu and Tineke van der Sluis. Their work appears in journals such as Human Genetics, Human Mutation, European Journal of Human Genetics, Genes Chromosomes and Cancer and Gastroenterology.

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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