Lodewijk Sandkuijl
Overview
Explore the profile of Lodewijk Sandkuijl including associated specialties, affiliations and a list of published articles.
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7
Citations
415
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Recent Articles
1.
Service S, Molina J, DeYoung J, Jawaheer D, Aldana I, Vu T, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2006 May;
141B(4):367-73.
PMID: 16652356
We have ascertained in the Central Valley of Costa Rica a new kindred (CR201) segregating for severe bipolar disorder (BP-I). The family was identified by tracing genealogical connections among eight...
2.
Hendriks Y, Wagner A, Morreau H, Menko F, Stormorken A, Quehenberger F, et al.
Gastroenterology
. 2004 Jul;
127(1):17-25.
PMID: 15236168
Background & Aims: Hereditary nonpolyposis colorectal carcinoma (HNPCC) is caused by a mutated mismatch repair (MMR) gene. The aim of our study was to determine the cumulative risk of developing...
3.
Weigell-Weber M, Sarra G, Kotzot D, Sandkuijl L, Messmer E, Hergersberg M
Arch Ophthalmol
. 2003 Aug;
121(8):1184-8.
PMID: 12912698
Objectives: To localize the gene that causes an autosomal recessively inherited vitreoretinal dystrophy that has not been described, to our knowledge, and to analyze a candidate gene mapped to 22q13...
4.
van der Hel O, Bueno de Mesquita H, Sandkuijl L, van Noord P, Pearson P, Grobbee D, et al.
Cancer Causes Control
. 2003 Jun;
14(3):293-8.
PMID: 12814209
Objective: The relationship between smoking and colorectal cancer risk and whether such effect is modified by variations in the NAT2 genotype is investigated. Methods: In the prospective DOM (Diagnostisch Onderzoek...
5.
Dankers M, Roelen D, Korfage N, de Lange P, Witvliet M, Sandkuijl L, et al.
Hum Immunol
. 2003 May;
64(6):600-6.
PMID: 12770790
More insight into the differential immunogenicity of human leukocyte antigen (HLA) mismatches will be beneficial for donor selection in clinical transplantation. In this study the immunogenicity of HLA antigens was...
6.
Groenewegen W, Firouzi M, Bezzina C, Vliex S, van Langen I, Sandkuijl L, et al.
Circ Res
. 2003 Jan;
92(1):14-22.
PMID: 12522116
Atrial standstill (AS) is a rare arrhythmia that occasionally appears to be genetically determined. This study investigates the genetic background of this arrhythmogenic disorder in a large family. Forty-four family...
7.
Lemmers R, de Kievit P, Sandkuijl L, Padberg G, van Ommen G, Frants R, et al.
Nat Genet
. 2002 Oct;
32(2):235-6.
PMID: 12355084
Contractions in the polymorphic D4Z4 repeat array of subtelomere 4qter cause autosomal dominant facioscapulohumeral muscular dystrophy in humans. A polymorphic segment of 10 kb directly distal to D4Z4 exists in...