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Genetics

D-Index
67
Citations
15320
World Ranking
2539
National Ranking
97

Overview

Lodewijk A. Sandkuijl was affiliated with Leiden University Medical Center in the Netherlands. Their professional work contributed to the academic and medical research community associated with this institution.

While there is limited detailed information on specific research topics, papers, or co-authors linked to Lodewijk A. Sandkuijl, the association with a prominent medical center suggests involvement in medical or biomedical research fields.

As there are no records of published papers, frequent co-authors, or common publication venues available, a detailed account of their scholarly output cannot be provided. Similarly, no information is available regarding book publications, main or subfields of study, or specific topics of research.

There are no recorded awards or recognitions documented for Lodewijk A. Sandkuijl. The data indicates that the scientist is deceased.

Best Publications

  • Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.

    Cisca Wijmenga;Jane E. Hewitt;Lodewijk A. Sandkuijl;Lorraine N. Clark

  • A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

    Njajou Ot;Vaessen N;Joosse M;Berghuis B

  • Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.

    Yvonne M C Hendriks;Anja Wagner;Hans Morreau;Fred Menko

  • PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

    C.M. van Duijn;M.C.J. Dekker;V. Bonifati;R.J. Galjaard

  • An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21.

    Johanna Aaltonen;Petra Björses;Lodewijk Sandkuijl;Jaakko Perheentupa

  • Genome screening by searching for shared segments: Mapping a gene for benign recurrent intrahepatic cholestasis

    Roderick H. J. Houwen;Siamak Baharloo;Kathleen Blankenship;Peter Raeymaekers

  • Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

    Petra G M van Overveld;Richard J F L Lemmers;Lodewijk A Sandkuijl;Leo Enthoven

  • Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.

    Kaate R.J. Vanmolkot;Esther E. Kors;Jouke Jan Hottenga;Gisela M. Terwindt

  • Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

    Gruis Na;van der Velden Pa;Sandkuijl La;Prins De

  • A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

    S.C. Bakker;E. M. van der Meulen;J.K. Buitelaar;L.A. Sandkuijl

  • A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

    W. Antoinette Groenewegen;Mehran Firouzi;Connie R. Bezzina;Saskia Vliex

  • Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

    D.J.M. Peters;L. Spruit;J.J. Saris;D. Ravine

  • Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.

    Richard J L F Lemmers;Peggy de Kievit;Lodewijk Sandkuijl;George W Padberg

  • Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23

    NB Freimer;[No Value] Reus;MA Escamilla;LA McInnes

  • Screening and Diagnosis for the Fragile X Syndrome Among the Mentally Retarded: An Epidemiological and Psychological Survey

    Bert B. A. de Vries;Ans M. W. van den Ouweland;Serieta Mohkamsing;Hugo J. Duivenvoorden

  • A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

    Heutink P;van der Mey Ag;Sandkuijl La;van Gils Ap

  • Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study

    Dieter B. Wildenauer;Sibylle G. Schwab;Margot Albus;Joachim Hallmayer

  • Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.

    Arne May;Roel A. Ophoff;Gisela M. Terwindt;Christine Urban

  • 17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations.

    Alm Boehmer;AO Brinkmann;LA Sandkuijl;Djj Halley

  • Melanocortin-1 Receptor Variant R151C Modifies Melanoma Risk in Dutch Families with Melanoma

    Pieter A. van der Velden;Lodewijk A. Sandkuijl;Wilma Bergman;Stan Pavel

Frequent Co-Authors

Peter Heutink
Peter Heutink German Center for Neurodegenerative Diseases
Ben A. Oostra
Ben A. Oostra Erasmus University Rotterdam
Nelson B. Freimer
Nelson B. Freimer University of California, Los Angeles
Rune R. Frants
Rune R. Frants Leiden University Medical Center
Cisca Wijmenga
Cisca Wijmenga University Medical Center Groningen
Guido J. Breedveld
Guido J. Breedveld Erasmus University Rotterdam
George W. Padberg
George W. Padberg Radboud University
Rune R. Frants
Rune R. Frants Leiden University
Nelleke A. Gruis
Nelleke A. Gruis Leiden University Medical Center
Peter L. Pearson
Peter L. Pearson Universidade de São Paulo

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