Janssens
AC, Pardo MC, Steyerberg EW, Duijn CM van. Revisiting
the clinical validity of multiplex genetic testing
in complex diseases. Am J Hum Gent 2004;74:585-8.
Sleegers
K, Roks G, Theuns J, Aulchenko YS, Rademakers R, Cruts
M, Gool WA van, Broeckhoven C van, Heutink P, Oostra
BA, Swieten JC van, Duijn CM van. Familial clustering
and genetic risk for dementia in a genetically isolated
Dutch population. Brain 2004;127:1-9.
Pocchiari
M, Puopolo M, Croes EA, Budka H, Gelpi E, Collins
S, Lewis V, Sutcliffe T, Guilivi A, Delasnerie-Laupretre
N, Brandel JP, Alperiovitch A, Zerr I, Poster S, Kretzschmar
HA, Ladogana A, Rietveld I, Mitrova E, Martinez-Martin
P, Pedro-Cuesta J de, Glatzel M, Aguzzi A, Cooper
S, Mackenzie J, Duijn CM van, Will RG. Predictors
of survial in sproadic Creutzfeldt-Jakob disease and
other human transmissible spongiform encephalopathies.
Brain 2004;127:2348-59.
Dekker MCJ,
Bonifati V, Duijn CM van. Parkinson's disease: piecing
together a genetic jigsaw. Brain 2003;126:1722-33.
Croes EA,
Dermaut B, Houwing-Duistermaat JJ, Broeck M van den,
Cruts M, Breteler MM, Hofman A, Broeckhoven C van,
Duijn CM van. Early cognitive decline is associated
with prion protein codon 129 polymorphism. Ann Neurol
2003;54:275-6.
Maitland-van
der Zee AH, Stricker BH, Klungel OH, Mantel-Teeuwisse
AK, Kastelein JJ, Hofman A, Leufkens HG, Duijn CM
van, Boer A de. Adherence to and dosing of beta-hydroxy-beta-methylglutaryl
coenzyme a reductase inhibitors differs according
to apolipoprotein E-genotypes. Pharmacogenetics 2003;13:219-23.
Aulchenko
YS, Vaessen N, Heutink P, Pullen J, Snijders PJLM,
Hofman A, Sandkuijl LA, Houwing-Duistermaat JJ, Edwards
M, Bennett S, Oostra BA, Duijn CM van. A genome-wide
search for genes involved in type 2 diabetes in a
recently genetically isolated population from the
Netherlands. Diabetes 2003;52:3001-4.
Bonifati
V, Rizzu P, Baren J van, Schaap O, Breedveld GJ, Krieger
E, Dekker MCJ, Squitieri F, Ibanez P, Joosse M, Dongen
JW van, VAnacore N, Swieten JC van, Brice A, Meco
G, Duijn CM van, Oostra BA, Heutink P. Mutations in
the DJ-1 gene associated with autosomal reccessive
early-onset parkinsonism. Science 2003;299:256-9.
Meijers-Heijboer
H, Ouweland A van den, Klijn J, Wasielewski M, Snoo
A de, Oldenburg R, Hollestelle A, Houben M, Crepin
E, Veghel M van, Elstrodt F, Duijn C van, Bartels
C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton
DF, Sodha N, Seal S, Barfoot R, Mangion J, Chang J,
Eccles D, Eeles R, Evans DG, Houlston R, Murday V,
Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo
C, Devilee P, Goldgar D, Futreal PA, Nathanson KL,
Weber BL, Rahman N, Stratton MR. Low-penetrance susceptibility
to breast cancer due to CHEK2*1100delC in noncarriers
of BRCA1 or BRCA2 mutations. Nat Genet 2002;31:55-9.
Chumakov
I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio
M, Abderrahim H, Bougueleret L, Barry C, Tanaka H,
La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse
S, Lissarrague S, Picard FP, Maurice K, Essioux L,
Millasseau P, Grel P, Debailleul V, Simon AM, Caterina
D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot
M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier
S, Nasroune M, Peixoto H, Delahaye A, Pinchot V, Bastucci
M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni
S, Aurich-Costa J, Cherif D, Gimalac A, Duijn C van,
et al. Genetic and physiological data implicating
the new human gene G72 and the gene for D-amino acid
oxidase in schizophrenia. Proc Natl Acad Sci U S
A 2002;99:13675-80.
Vaessen
N, Janssen JA, Heutink P, Hofman A, Lamberts SWJ,
Oostra BA, Pols HAP, Duijn CM van. Genetic variation
in the gene for insulin-like growth factor-I is associated
with low birthweight. Lancet 2002;359:1036-7.
Ruitenberg
A, Swieten JC van, Witteman JC, Mehta KM, Duijn CM
van, Hofman A, Breteler MM. Alcohol consumption and
risk of dementia: The Rotterdam Study. Lancet 2002;359:281-6.
Njajou OT,
Vaessen N, Joosse M, Berghuis B, Dongen JWF van, Breuning
MH, Snijders PJLM, Rutten WPF, Sandkuijl LA, Oostra
BA, Duijn CM van, Heutink P. A mutation in SLC11A3
gene is associated with autosomal dominant hematochromatosis.
Nat Genet 2001;28:214-5
Ott A, Slooter
AJC, Hofman A, Harskamp F van, Witteman JCM, Broeckhoven
C van, Duijn CM van, Breteler MMB. Smoking and the
risk of dementia and Alzheimer's disease in a population-baseed
cohort study: the Rotterdam Study. Lancet 1998;351:1840-3.
Klaver CCW,
Kliffen M, Duijn CM van, Hofman A, Cruts M, Grobbee
DE, Broeckhoven C van, Jong PTVM de. Genetic association
of apolipoprotein E with age related macular degeneration.
Am J Hum Genet 1998;63:200-6.
Klaver CCW,
Assink JJM, Bergen AAB, Duijn CM van. Re: ABCR gene
and age-related macular degeneration. Science 1998;279:1107.
Will RG,
Alperovitch A, Poser S, Pocchiari M, Hofman A, Mitrova
E, Silva R de, DÁlesandro M, Brandel J-P, Zerr
I, Duijn CM van. Creutzfeldt-Jakob disease in Europe
1993-1995. Descriptive epidemiology. For the EU Collaborative
Study Group for CJD. Ann Neurol 1998;43:763-7.
Duijn CM
van, Delasnerie-Laupretre N, Masullo C, Zerr I, Silva
R de, Wientjens DPWM, Brandel J-P, Weber T, Bonavita
V, Zeidler M, Alperovitch A, Poser S, Granieri E,
Hofman A, Will RG. For the EU Collaborative Study
Group for CJD. Case-control study of risk factors
of Creutzfeldt-Jakob disease in Europe during 1993-1995.
Lancet 1998;351:1081-5.
Hofman A,
Ott A, Breteler MMB, Bots ML, Slooter AJC, Harskamp
F van, Duijn CM van, Broeckhoven C van, Grobbee DE.
Atherosclerosis, apolipoprotein E and the prevalence
of dementia and Alzheimer's disease in a population-based
study: the Rotterdam Study. Lancet 1997;349:151-4.
Farrer LA,
Cupples LA, Haines JL, Hyman B, Kukull WA, Mayeux
R, Myers MH, Pericak-Vance MA, Risch N, Duijn CM van;
for APOE and Alzheimer's Disease Meta-Analysis Consortium.
Effects of age, gender and ethnicity on the association
between apolipoprotein E genotype and Alzheimer's
disease. JAMA 1997;278:1349-56.
Slooter
A, Breter MMB, Ott A, Broeckhoven C van, Duijn CM
van. APOE genotyping in differential diagnosis of
Alzheimer's disease. Lancet 1996;348:334.
Duijn CM
van, Broeckhoven C van, Knijff P de, Cruts M, Wehnert
A, Havekes LM, Hofman A. Smoking and apolipoprotein
E e4
allele and the risk of early-onset Alzheimer's disease.
BMJ 1995;310:627-31.
Duijn
CM van, Broeckhoven C van. Alzheimer's disease and
the family effect. Nat Genetics 1994;8:115.
Duijn
CM van, Knijff P van, Cruts M, Wehnert A, Havekes
LM, Hofman A, Broeckhoven C van. Apolipoprotein E
E4 allele in a population-based study of early-onset
Alzheimer's disease. Nat Genetics 1994;7:74-8.
Duijn CM
van, Hendriks L, Farrer LA, Backhovens H, Cruts M,
Wehnert A, Hofman A, Broeckhoven C van. Linkage to
chromosome 14, 19 and 21 in families derived from
a population-based study of Alzheimer's disease. Am
J Hum Genet 1993;53:871.
Hendriks
L, Duijn CM van, Cras P, Cruts M, Hul W van, Harskamp
F van, Warren A, McInnis MG, Antonarakis SE, Martin
J-J, Hofman A, Broeckhoven C van. Presenile dementia
and cerebral haemorrhage linked to a mutation at codon
692 of the ß-amyloid precursor protein gene.
Nat Genet 1992;1:218-221.
Duijn CM
van, Hendriks L, Cruts M, Hardy JA, Hofman A, Broeckhoven
C van. Frequency of mutation in the amyloid precursor
protein gene. Lancet 1991;337:978.
Hofman A,
Duijn CM van, Rocca WA. Is Alzheimer's disease distinct
from normal ageing? Lancet 1988;ii:226-7.
Duijn CM
van, Steensel-Moll HA van, Does-vander Berg A van
der, Wering ER van, Zanen GE van, Valkenburg HA, Rammeloo
JA. Infant feeding and childhood cancer. Lancet 1988;ii:796-7.
Kok FJ,
Duijn CM van, Hofman A, Vermeeren R, Bruijn AM de,
Valkenburg HA. Micronutrients and the risk of lung
cancer. N Engl J Med 1987;316:1416.
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