Edwin Verlind

979 citations

27 papers · 704 · h-index 15

Impact in

Pathology and Forensic Medicine top 5%
- Genetic factors in colorectal cancer
Genetics
- Glioma Diagnosis and Treatment

Papers in

Genetics 8
- Genomic variations and chromosomal abnormalities 4
- Genetic Associations and Epidemiology 4
- Chronic Lymphocytic Leukemia Research 2
Pathology and Forensic Medicine 5
- Genetic factors in colorectal cancer 5

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

In The Last Decade

Edwin Verlind

27 papers receiving 672 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

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#	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 A. Kooi, Tineke van der Sluis, Claudia Kempinga	2001	132
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	2001	129
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	57
4	Three novel KCNA1 mutations in episodic ataxia type I families Human Genetics ·Hans Scheffer, Ewout R. P. Brunt, Pieter van der Vlies, Not Available Not Available, Edwin Verlind, G.W.H. Mantel, Yu. N. Averyanov, Robert M.W. Hofstra	1998	52
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. Schuilenga‐Hut, Pieter van der Vlies, Edwin Verlind, Charles H.C.M. Buys, Hans Scheffer, Marcel F. Jonkman, Hiroshi Shimizu	2000	38
7	Comprehensive TP53-Denaturing Gradient Gel Electrophoresis Mutation Detection Assay Also Applicable to Archival Paraffin-Embedded Tissue Diagnostic Molecular Pathology ·Vanessa M. Hayes, Wim A. Bleeker, Edwin Verlind, Tineke Timmer, Arend Karrenbeld, John Th. M. Plukker, Munro P. Marx, Robert M.W. Hofstra	1999	26
8	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
9	X-linked hydrocephalus: a novel missense mutation in the L1CAM gene Pediatric Neurology ·László Sztriha, Yvonne J. Vos, Edwin Verlind, Bertel Berg +1 other	2002	21
10	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 V. Baranova, Chantal Lummen, Tatiana V. Tyazhelova, Maaike W.G. Looman, Dmitry Ivanov, Edwin Verlind, Anna Pestova	2003	21
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 A. Bleeker, Vanessa M. Hayes, Arend Karrenbeld, Robert M.W. Hofstra, Edwin Verlind, J. Hermans, Sibrand Poppema, Charles H. C. M. Buys	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 Kenneth Cowell	1995	19
13	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	19
14	New comprehensive denaturing‐gradient‐gel‐ electrophoresis assay for KRAS mutation detection applied to paraffin‐embedded tumours Genes Chromosomes and Cancer ·Vanessa M. Hayes, Jantine L. Westra, Edwin Verlind, Wim A. Bleeker, John Th. M. Plukker, Robert M.W. Hofstra, Charles H.C.M. Buys	2000	17
15	RAPID SCREENING FOR ΔF508 DELETION IN CYSTIC FIBROSIS The Lancet ·J S Noble, June Hall, Philip Quirke, Alistair D. Stewart, Raquel Rodrigues Mueller, Hans Scheffer, Edwin Verlind, Dirk Penninga	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, Leena Bruckner‐Tuderman, Tobias Gedde‐Dahl, G.J. te Meerman, Arnoud Sonnenberg, Charles H.C.M. Buys	1997	14
17	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
18	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	9
19	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
20	A Deletion Hybrid Breakpoint Map of the Chromosomal Region 13q14-q21 Orders 19 Genetic Markers in 10 Intervals European Journal of Human Genetics ·R. Frank Kooy, Edwin Verlind, Roderick H.J. Houwen, David N. Shapiro, Lesleyann Hawthorn, John Kenneth Cowell, Hans Scheffer, Charles H.C.M. Buys	1994	7

About Edwin Verlind

Edwin Verlind is a scholar working on Genetics, Pathology and Forensic Medicine, Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 27 papers that have together received 704 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic Associations and Epidemiology (4 papers), Fetal and Pediatric Neurological Disorders (3 papers), Glycogen Storage Diseases and Myoclonus (3 papers), Trace Elements in Health (2 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Skin and Cellular Biology Research (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (203 citations), Genetics (55 citations), Rheumatology (67 citations), Cell Biology (49 citations) and Genetics (93 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, Harry Hollema, Maran J.W. Berends, Jan H. Kleibeuker, Rob G.J. Mensink, Rolf H. Sijmons, Tineke van der Sluis and Ying Wu. Their work appears in journals such as Human Genetics, Human Mutation, European Journal of Human Genetics, The Lancet and Genes Chromosomes and Cancer.

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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