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L. Went · SciRah

Researcher profile · Semantic Scholar

L. Went

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L. Went — researcher profile on SciRah

h-index: 30
Works: 128
Citations: 3,043

Most-cited papers

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.
D. Devries, L. Went, G. Bruyn, H. Scholte +3 more
1996American Journal of Human Genetics205 citations
Semantic Scholar
Familial cerebral amyloid angiopathy presenting as recurrent cerebral haemorrhage.
A. Wattendorff, G. Bots, L. Went, L. Endtz
1982Journal of Neurological Sciences161 citations
Semantic Scholar
Guidelines for the molecular genetics predictive test in Huntington's disease
L. Went, J. Broholm, J. Cassiman, D. Craufurd +15 more
1994158 citations
Semantic Scholar
Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology.
L. Went
1990Journal of Medical Genetics140 citations Open access
Semantic Scholar
Genetic aspects of erythropoietic protoporphyria
L. Went, E. Klasen
1984Annals of Human Genetics125 citations
Semantic Scholar
Tumour spectrum in the FAMMM syndrome.
Henry T. Lynch, R. Fusaro, J. Pester, J. Oosterhuis +4 more
1981British Journal of Cancer120 citations Open access
Semantic Scholar
Hereditary cerebral haemorrhage caused by cortical amyloid angiopathy.
W. Luyendijk, G. Bots, M. D. der Vlis, L. Went +1 more
1988Journal of Neurological Sciences113 citations
Semantic Scholar
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.
C. Weitz, Yozo Miyake, K. Shinzato, E. Montag +3 more
1992American Journal of Human Genetics98 citations
Semantic Scholar
Protoporphyrin-induced photohemolysis in protoporphyria and in normal red blood cells.
A. Schothorst, J. van Steveninck, L. Went, D. Suurmond
1970Clinica chimica acta; international journal of clinical chemistry96 citations
Semantic Scholar
Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment.
C. Weitz, L. Went, J. Nathans
1992American Journal of Human Genetics92 citations
Semantic Scholar
Clinical and genetic studies in six Dutch kindreds with the Dysplastic Naevus Syndrome
W. Bergman, A. Palan, L. Went
1986Annals of Human Genetics86 citations
Semantic Scholar
Photodynamic damage of the erythrocyte membrane caused by protoporphyrin in protoporphyria and in normal red blood cells.
A. Schothorst, J. van Steveninck, L. Went, D. Suurmond
1972Clinica chimica acta; international journal of clinical chemistry83 citations
Semantic Scholar
Studies on African Pygmies. I. A pilot investigation of Babinga Pygmies in the Central African Republic (with an analysis of genetic distances).
L. Cavalli-sforza, L. A. Zonta, F. Nuzzo, L. Bernini +8 more
1969American Journal of Human Genetics79 citations
Semantic Scholar
Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
P. Milner, Colin Miller, Robert Grey, Michael Seakins +2 more
1970New England Journal of Medicine78 citations
Semantic Scholar
A SEX-LINKED HEREDO-DEGENERATIVE NEUROLOGICAL DISORDER, ASSOCIATED WITH LEBER'S OPTIC ATROPHY. I. CLINICAL STUDIES.
G. Bruyn, L. Went
1964Journal of Neurological Sciences70 citations
Semantic Scholar
Primary choroidal and cutaneous melanomas, bilateral choroidal melanomas, and familial occurrence of melanomas.
J. Oosterhuis, L. Went, Henry T. Lynch
1982British Journal of Ophthalmology66 citations Open access
Semantic Scholar
A New Genetic Variant of β-Thalassaemia
R. C. Schokker, L. Went, J. Bok
1966Nature49 citations
Semantic Scholar
Results of a sedimentation technique for cytology of cerebrospinal fluid.
G. Bots, L. Went, A. Schaberg
1964Acta Cytologica44 citations
Semantic Scholar
Oculomotor defects in patients with Huntington's disease and their offspring.
H. Collewijn, L. Went, E. P. Tamminga, M. D. der Vlis
1988Journal of Neurological Sciences43 citations
Semantic Scholar
Spinal cord compression due to extramedullary hematopoiesis in homozygous thalassemia. Case report.
W. Luyendijk, L. Went, Hans-Peter Schaad
1975Journal of Neurosurgery43 citations
Semantic Scholar
Hereditary compression syndrome of peripheral nerves
A. Staal, C. de Weerdt, L. Went
1965Neurology43 citations
Semantic Scholar
Metabolic aspects of the photodynamic effect of protoporphyrin in protoporphyria and in normal red blood cells.
A. Schothorst, J. van Steveninck, L. Went, D. Suurmond
1971Clinica chimica acta; international journal of clinical chemistry42 citations
Semantic Scholar
Haemoglobin Leiden: Deletion of β6 or 7 Glutamic Acid
W. D. de Jong, L. Went, L. Bernini
1968Nature40 citations
Semantic Scholar
-Carotene as a treatment for photohypersensitivity due to erythropoietic protoporphyria.
H. Baart de la Faille, D. Suurmond, L. Went, J. van Steveninck +1 more
1972Dermatologica37 citations
Semantic Scholar
NEUROLOGICAL STUDIES IN FAMILIES WITH LEBER'S OPTIC ATROPHY
C. de Weerdt, L. Went
1971Acta Neurologica Scandinavica37 citations Open access
Semantic Scholar
The genetics of tritan disturbances
L. Went, N. Pronk
2004Human Genetics32 citations
Semantic Scholar
X-linked incomplete achromatopsia with more than one class of functional cones.
Vivianne C. Smith, J. Pokorny, J. Delleman, M. Cozijnsen +2 more
1983Investigative Ophthalmology and Visual Science29 citations
Semantic Scholar
Hereditary spastic dystonia: a new mitochondrial encephalopathy? Putaminal necrosis as a diagnostic sign.
G. Bruyn, G. Vielvoye, L. Went
1991Journal of Neurological Sciences25 citations
Semantic Scholar
Parental transmission in Huntington's disease.
L. Went, M. D. der Vlis, G. Bruyn
1984The Lancet25 citations
Semantic Scholar
Huntington's Chorea in the Netherlands The problem of genetic heterogeneity
L. Went, M. D. der Vlis, G. Bruyn, W. S. Volkers
1983Annals of Human Genetics24 citations
Semantic Scholar
X‐linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred
L. Went, W. D. de Groot, R. Sanger, P. Tippett +1 more
1969Annals of Human Genetics24 citations
Semantic Scholar
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.
Monique Losekoot, R. Fodde, C. Harteveld, H. van Heeren +3 more
1991Journal of Medical Genetics20 citations Open access
Semantic Scholar
Familial hypokalemic periodic paralysis. 50-year follow-up of a large family.
O. Buruma, G. Bots, L. Went
1985Archives of Neurology20 citations
Semantic Scholar
Juvenile amyotrophic lateral sclerosis-dementia complex in a Dutch family
A. Staal, L. Went
1968Neurology20 citations
Semantic Scholar
Binding of Protoporphyrin to hemoglobin in red blood cells of patients with erythropoietic protoporphyria.
J. van Steveninck, T. M. Dubbelman, A. D. de Goeij, L. Went
1977Hemoglobin19 citations
Semantic Scholar
SOME CLINICAL AND FUNDAMENTAL ASPECTS OF ERYTHROPOIETIC PROTOPORPHYRIA
D. Suurmond, J. Steveninck, L. Went
1970British Journal of Dermatology19 citations
Semantic Scholar
Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings.
G. Bruyn, G. Bots, L. Went, P. Klinkhamer
1992Journal of Neurological Sciences18 citations
Semantic Scholar
Ages of death of children with Huntington's Chorea and of their affected parents
M. D. der Vlis, W. S. Volkers, L. Went
1976Annals of Human Genetics18 citations
Semantic Scholar
A search for associations between genetical polymorphic systems and physical, biochemical and Haematological variables.
G. Fraser, W. Volkers, L. F. Bernini, W. B. de Greve +6 more
1974Human Heredity14 citations
Semantic Scholar
Genetic linkage between erythrokeratodermia variabilis and Rh locus
J. van der Schroeff, L. Nijenhuis, P. Khan, L. F. Bernini +4 more
2004Human Genetics13 citations
Semantic Scholar
Studies in dominant optic atrophy.
H. Roggeveen, A. D. de Winter, L. Went
1985Ophthalmic Paediatrics and Genetics13 citations
Semantic Scholar
Leber hereditary optic neuropathy (LHON): a mitochondrial disease with unresolved complexities
L. Went
1999Cytogenetic and Genome Research12 citations
Semantic Scholar
[Familial cerebral hemorrhage as a result of cerebral amyloid angiopathy].
W. Luyendijk, G. Bots, M. D. der Vlis, L. Went
1986Nederlandsch tijdschrift voor geneeskunde11 citations
Semantic Scholar
Genetic linkage studies in Huntington's chorea
W. S. Volkers, L. Went, M. D. der Vlis, P. S. Harper +1 more
1980Annals of Human Genetics11 citations
Semantic Scholar
A new genetic variant of beta-thalassaemia.
R. C. Schokker, L. Went, J. Bok
1966Nature11 citations
Semantic Scholar
A FAMILY WITH HEREDITARY SPASTIC ATAXIA
G. T. Beusekom, A. Staal, L. Went
1965Acta Neurologica Scandinavica11 citations
Semantic Scholar
Early diagnosis and prevention of genetic diseases.
L. Went, C. Vermeij-Keers, A. Van der Linden
19759 citations
Semantic Scholar
The colour vision characteristics of an observer with unilateral defective colour vision: results and analysis.
B. G. Bender, K. Ruddock, E. C. De Vries-De Mol, L. Went
1972Vision Research9 citations
Semantic Scholar
A sex-linked heredo-degenerative neurological disorder, associated with Leber's optic atrophy: Part 2. Laboratory investigation
L. Went
19649 citations
Semantic Scholar
The familial occurrence of cutaneous melanoma, intraocular melanoma, and the dysplastic nevus syndrome.
R. Fusaro, Henry T. Lynch, J. Oosterhuis, L. Went
1984American journal of ophthalmology-glaucoma8 citations
Semantic Scholar

Frequent co-authors

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M. D. der Vlis×7
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M. D. der Vlis — researcher profile on SciRah
G. Bruyn×6
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G. Bots×6
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J. van Steveninck×5
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×5

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D. Suurmond — researcher profile on SciRah

A. Schothorst×4

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Henry T. Lynch×3

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Henry T. Lynch — researcher profile on SciRah

J. Oosterhuis×3

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J. Oosterhuis — researcher profile on SciRah

W. Luyendijk×3

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W. Luyendijk — researcher profile on SciRah

W. D. de Jong×3

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W. D. de Jong — researcher profile on SciRah

L. Nijenhuis×3

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L. Nijenhuis — researcher profile on SciRah

E. van Loghem×3

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E. van Loghem — researcher profile on SciRah