Publikationen in Zusammenarbeit mit Forschern von University of Lille Nord de France (19)

2022

  1. New insights into the genetic etiology of Alzheimer's disease and related dementias

    Nature genetics, Vol. 54, Núm. 4, pp. 412-436

2021

  1. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

    Nature communications, Vol. 12, Núm. 1, pp. 3417

2019

  1. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)

    Nature Genetics

  2. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Nature Genetics, Vol. 51, Núm. 3, pp. 414-430

  3. Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease

    Translational Psychiatry, Vol. 9, Núm. 1

2017

  1. Erratum to: Identification and management of patients at increased risk of osteoporotic fracture: outcomes of an ESCEO expert consensus meeting (Osteoporosis International, (2017), 28, 7, (2023-2034), 10.1007/s00198-017-4009-0)

    Osteoporosis International

  2. Identification and management of patients at increased risk of osteoporotic fracture: outcomes of an ESCEO expert consensus meeting

    Osteoporosis International, Vol. 28, Núm. 7, pp. 2023-2034

  3. Transcatheter Aortic Valve Replacement in Pure Native Aortic Valve Regurgitation

    Journal of the American College of Cardiology, Vol. 70, Núm. 22, pp. 2752-2763

2015

  1. Convergent genetic and expression data implicate immunity in Alzheimer's disease

    Alzheimer's and Dementia, Vol. 11, Núm. 6, pp. 658-671

2014

  1. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

    PLoS ONE, Vol. 9, Núm. 6

2013

  1. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

    Molecular Psychiatry, Vol. 18, Núm. 4, pp. 461-470

  2. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

    Nature Genetics, Vol. 45, Núm. 12, pp. 1452-1458

  3. Thyroid hormone receptor alpha gene variants increase the risk of developing obesity and show gene-diet interactions

    International Journal of Obesity, Vol. 37, Núm. 11, pp. 1499-1505

2011

  1. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

    Nature Genetics, Vol. 43, Núm. 5, pp. 429-436

  2. Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations

    Neurobiology of Aging, Vol. 32, Núm. 4, pp. 756.e11-756.e15

2010

  1. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: A meta-analysis study

    Journal of Alzheimer's Disease, Vol. 22, Núm. 1, pp. 247-255

2009

  1. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

    Nature Genetics, Vol. 41, Núm. 10, pp. 1094-1099

2006

  1. Patients enrolled in coronary intervention trials are not representative of patients in clinical practice: Results from the Euro Heart Survey on Coronary Revascularization

    European Heart Journal, Vol. 27, Núm. 6, pp. 671-678

2005

  1. Management and outcome of patients with established coronary artery disease: The Euro Heart Survey on coronary revascularization

    European Heart Journal, Vol. 26, Núm. 12, pp. 1169-1179