D. B. van Dorp

525 citations

21 papers · 410 · h-index 13

Impact in

Cell Biology top 10%
- melanin and skin pigmentation
Ophthalmology top 10%
- Retinal Diseases and Treatments

Papers in

Cell Biology 10
- melanin and skin pigmentation 10
Molecular Biology 9
- Retinal Development and Disorders 6
- Retinoids in leukemia and cellular processes 4

Co-authors: Alan F. Wright (5 shared papers)J.W. Delleman (4 shared papers)P. Wijermans (2 shared papers)Andrew D. Carothers (1 shared paper)Arthur A. Bergen (4 shared papers)M. L. Kwee (3 shared papers)Katherine L. Dry (4 shared papers)Forbes Manson (2 shared papers)
Journals: Clinical Genetics (5 papers)Human Genetics (2 papers)Human Mutation (2 papers)Genomics (1 paper)Ophthalmic Genetics (1 paper)
Partner nations: Netherlands United Kingdom Germany

In The Last Decade

D. B. van Dorp

21 papers receiving 392 citations

Peers

Countries citing papers authored by D. B. van Dorp

Since Specialization

Citations

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

Fields of papers citing papers by D. B. van Dorp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. B. van Dorp. 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 D. B. van Dorp. The network helps show where D. B. van Dorp may publish in the future.

Co-authors

The 25 scholars most cited alongside D. B. van Dorp, 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 D. B. van Dorp Line = papers co-authored together D. B. van Dorp 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 21 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities Human Genetics ·D. B. van Dorp, Alan F. Wright, Andrew D. Carothers, Elizabeth M. Bleeker-Wagemakers	1992	71
2	Identification of a 5? splice site mutation in theRPGR gene in a family with X-linked retinitis pigmentosa (RP3) Human Mutation ·Katherine L. Dry, Forbes Manson, Alan Lennon, Arthur A. Bergen, D. B. van Dorp, Alan F. Wright	1999	35
3	Hermansky‐pudlak syndrome: Correction of bleeding time by 1‐desamino‐8D‐arginine vasopressin American Journal of Hematology ·P. Wijermans, D. B. van Dorp	1989	31
4	Joubert syndrome: A clinical and pathological description of an affected male and a female fetus from the same sibship American Journal of Medical Genetics ·D. B. van Dorp, Alzbeta Palan, M. L. Kwee, P. G. Barth, Johan J. van der Harten	1991	31
5	Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type Human Genetics ·Arthur A. Bergen, C. Samanns, E. J. M. Schuurman, Loes Van Osch, D. B. van Dorp, A. Pinckers, Egbert Bakker, A. Gal, G.J.B. van Ommen, E. M. Bleeker‐Wagemakers	1991	31
6	Åland eye disease: no albino misrouting Clinical Genetics ·D. B. van Dorp, Aldur W. Eriksson, J.W. Delleman, A.G.M. van Vliet, H. Collewijn, A. Th. M. van Balen, H Forsius	1985	27
7	A Family with X-Chromosomal Recessive Congenital Cataract, Microphthalmia, a Peculiar Form of the Ear and Dental Anomalies Journal of Pediatric Ophthalmology & Strabismus ·D. B. van Dorp, J.W. Delleman	1979	27
8	Kabuki syndrome ? Report of six cases and review of the literature with emphasis on ocular features Ophthalmic Genetics ·Irma Kluijt, D. B. van Dorp, M. L. Kwee, Annick Toutain, Kim M. Keppler‐Noreuil, Mette Warburg, Pierre Bitoun	2000	25
9	Oculocutaneous albinism and anterior chambre cleavage malformations Clinical Genetics ·D. B. van Dorp, J.W. Delleman, D.H. Loewer-Sieger	1984	19
10	Albinism, or the NOACH syndrome Clinical Genetics ·D. B. van Dorp	1987	19
11	The Hermansky-Pudlak syndrome: Variable reaction to 1-desamino-8D-arginine vasopressin for correction of the bleeding time Ophthalmic Paediatrics and Genetics ·D. B. van Dorp, P. Wijermans, Françoise Meire, Gijs F.J.M. Vrensen	1990	19
12	Linkage analysis in X-linked congenital stationary night blindness Genomics ·Micheala A. Aldred, Katherine L. Dry, Dianne Sharp, D. B. van Dorp, Janine L. Brown, L J Hardwick, Douglas H. Lester, Fiona Pryde, Peter Teague, Marcelle Jay, Alan C. Bird, (unknown), Alan F. Wright	1992	16
13	Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis Ophthalmic Paediatrics and Genetics ·Arthur A. Bergen, C. Samanns, D. B. van Dorp, M.A. Ferguson‐Smith, A. Gal, E. M. Bleeker‐Wagemakers	1990	14
14	Albinism: phenotype or genotype? Documenta Ophthalmologica ·D. B. van Dorp, N.J. van Haeringen, J.W. Delleman, Patricia Apkarian, W. Westerhof	1983	11
15	Evaluation of hairbulb incubation test and tyrosinase assay in the classification of albinism Ophthalmic Paediatrics and Genetics ·D. B. van Dorp, N.J. van Haeringen, E. Glasius	1982	11
16	Identification of a 5′ splice site mutation in the RPGR gene in a family with X‐linked retinitis pigmentosa (RP3) Human Mutation ·Katherine L. Dry, Forbes Manson, Alan Lennon, Arthur A. Bergen, D. B. van Dorp, Alan F. Wright	1999	11
17	Linkage analysis‐in a family with complete type congenital stationary night blindness with and without myopia Clinical Genetics ·Katherine L. Dry, D. B. van Dorp, Micheala A. Aldred, Janine L. Brown, L J Hardwick, Alan F. Wright	1993	5
18	Ultrastructure of the skin of human albinos Ophthalmic Paediatrics and Genetics ·J. T. W. Broodbakker, W. Westerhof, D. B. van Dorp	1983	3
19	Tuberous sclerosis Diagnostic problems in a family Ophthalmic Paediatrics and Genetics ·D. B. van Dorp, M. L. Kwee	1990	2
20	Carrier detection in X‐linked ocular albinism of the Nettleship‐Falls type by DNA analysis Clinical Genetics ·Anstein Bergan, L J. M. Schuurman, L. Ingeborgh van den Born, G. Samanns, D. B. van Dorp, A. Pinckers, Egbert Bakker, G.J.B. van Ommen, A. Gal, E. M. Bleeker‐Wagemakers	1992	1

About D. B. van Dorp

D. B. van Dorp is a scholar working on Cell Biology, Molecular Biology, Genetics, Ophthalmology and Physiology, having authored 21 papers that have together received 410 indexed citations. Recurring topics across this work include melanin and skin pigmentation (10 papers), Retinal Development and Disorders (6 papers), Retinoids in leukemia and cellular processes (4 papers), Glaucoma and retinal disorders (3 papers), Dye analysis and toxicity (3 papers), Thermoregulation and physiological responses (2 papers), Skin Protection and Aging (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Cell Biology (128 citations), Ophthalmology (49 citations), Genetics (133 citations), Molecular Biology (227 citations) and Sensory Systems (11 citations). D. B. van Dorp has collaborated with scholars based in Netherlands, United Kingdom and Germany. Frequent co-authors include Alan F. Wright, J.W. Delleman, P. Wijermans, Andrew D. Carothers, Arthur A. Bergen, M. L. Kwee, Katherine L. Dry, Forbes Manson, Alan Lennon and N.J. van Haeringen. Their work appears in journals such as Clinical Genetics, Human Genetics, Human Mutation, Genomics and Ophthalmic Genetics.

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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D. B. van Dorp

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