- Title
- Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease
- Creators
- Henne Holstege - Delft University of TechnologyMarc Hulsman - Delft University of TechnologyCamille Charbonnier - Université de Rouen NormandieBenjamin Grenier-Boley - Institut PasteurOlivier Quenez - Université de Rouen NormandieDetelina Grozeva - Cardiff UniversityJeroen G J van RooijRebecca Sims - Cardiff UniversityShahzad Ahmad - Erasmus University RotterdamNajaf Amin - Erasmus University RotterdamPenny J Norsworthy - MRC Prion UnitOriol Dols-Icardo - Hospital de Sant PauHolger Hummerich - MRC Prion UnitAmit Kawalia - University of ColognePhilippe Amouyel - Institut PasteurGary W Beecham - GenomicsClaudine Berr - Institute for Neurosciences of MontpellierJoshua C Bis - University of WashingtonAnne Boland - Atomic Energy and Alternative Energies CommissionPaola Bossù - Fondazione Santa LuciaFemke Bouwman - Vrije Universiteit AmsterdamJose Bras - Van Andel InstituteDominique Campion - Université de Rouen NormandieJ Nicholas Cochran - HudsonAlpha Institute for BiotechnologyAntonio Daniele - Università Cattolica del Sacro CuoreJean-François Dartigues - Bordeaux Population HealthStéphanie Debette - Bordeaux Population HealthJean-François Deleuze - Atomic Energy and Alternative Energies CommissionNicola Denning - Cardiff UniversityAnita L DeStefano - Framingham Heart StudyLindsay A Farrer - Boston UniversityMaria Victoria Fernández - Washington University in St. LouisNick C Fox - UCL AustraliaDaniela Galimberti - Fondazione IRCCS Ca' Granda Ospedale Maggiore PoliclinicoEmmanuelle Genin - Centre Hospitalier Régional Universitaire de BrestJohan J P Gille - Amsterdam UMC Location VUmcYann Le Guen - Stanford UniversityRita Guerreiro - Van Andel InstituteJonathan L Haines - Case Western Reserve UniversityClive Holmes - University of SouthamptonM Arfan Ikram - Erasmus University RotterdamM Kamran Ikram - Erasmus University RotterdamIris E Jansen - Amsterdam NeuroscienceRobert Kraaij - Erasmus University RotterdamMarc Lathrop - McGill University and Génome Québec Innovation CentreAfina W Lemstra - Amsterdam NeuroscienceAlberto Lleó - Hospital de Sant PauLauren Luckcuck - Cardiff UniversityMarcel M A M Mannens - University of AmsterdamRachel Marshall - Cardiff UniversityEden R Martin - Dr. John T. Macdonald FoundationCarlo Masullo - Università Cattolica del Sacro CuoreRichard Mayeux - Columbia UniversityPatrizia Mecocci - University of PerugiaAlun Meggy - Cardiff UniversityMerel O Mol - Erasmus University RotterdamKevin Morgan - University of NottinghamRichard M Myers - HudsonAlpha Institute for BiotechnologyBenedetta Nacmias - University of FlorenceAdam C Naj - University of PennsylvaniaValerio Napolioni - Stanford UniversityFlorence Pasquier - University of LillePau Pastor - University Hospital Mútua de TerrassaMargaret A Pericak-Vance - Dr. John T. Macdonald FoundationRachel Raybould - Cardiff UniversityRichard Redon - Centre National pour la Recherche Scientifique et Technique (CNRST)Marcel J T Reinders - Delft University of TechnologyAnne-Claire Richard - Université de Rouen NormandieSteffi G Riedel-Heller - Leipzig UniversityFernando Rivadeneira - Erasmus University RotterdamStéphane Rousseau - Université de Rouen NormandieNatalie S Ryan - UCL AustraliaSalha Saad - Cardiff UniversityPascual Sanchez-Juan - Universidad de CantabriaGerard D Schellenberg - University of PennsylvaniaPhilip Scheltens - Amsterdam NeuroscienceJonathan M Schott - UCL AustraliaDavide Seripa - STEMSudha Seshadri - Framingham Heart StudyDaoud Sie - Amsterdam UMC Location VUmcErik A Sistermans - Amsterdam UMC Location VUmcSandro Sorbi - University of FlorenceResie van SpaendonkGianfranco Spalletta - Fondazione Santa LuciaNiccolo' TesiBetty Tijms - Vrije Universiteit AmsterdamAndré G Uitterlinden - Erasmus University RotterdamSven J van der Lee - Amsterdam NeurosciencePieter Jelle Visser - Vrije Universiteit AmsterdamMichael Wagner - University Hospital BonnDavid Wallon - Université de Rouen NormandieLi-San Wang - University of PennsylvaniaAline Zarea - Université de Rouen NormandieJordi Clarimon - Hospital de Sant PauJohn C van Swieten - Erasmus University RotterdamMichael D Greicius - Stanford UniversityJennifer S Yokoyama - University Memory and Aging CenterCarlos Cruchaga - Washington University in St. LouisJohn Hardy - UCL AustraliaAlfredo Ramirez - University of CologneSimon Mead - MRC Prion UnitWiesje M van der Flier - Amsterdam NeuroscienceCornelia M van Duijn - Erasmus University RotterdamJulie Williams - Cardiff UniversityGaël Nicolas - Université de Rouen NormandieCéline Bellenguez - Institut PasteurJean-Charles Lambert - Institut Pasteur
- Publication Details
- Nature genetics
- Academic Unit
- Miller School of Medicine; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation); John P. Hussman Institute for Human Genomics
- Language
- English
- Resource Type
- Journal article
- Record Identifier
- 991031754608702976
Journal article
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease
Nature genetics
2022-11-21
Metrics
5 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.52 Neurodegenerative Diseases
- 1.52.57 Alzheimer's Disease
- Web Of Science research areas
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites