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المؤلفون: Annemieke J.M. Rozemuller, Diana A. T. Nijholt, John C. van Swieten, André G. Uitterlinden, Jeroen van Rooij, Shami Melhem, Tsz Hang Wong, Lieke H.H. Meeter, Joyce G. van Meurs
المساهمون: Netherlands Institute for Neuroscience (NIN), Internal Medicine, Neurology, Pathology, Amsterdam Neuroscience - Neurodegeneration
المصدر: Neurobiology of Aging, 74, 225-233. Elsevier B.V.
Neurobiology of Aging, 74, 225-233. Elsevier Inc.
van Rooij, J G J, Meeter, L H H, Melhem, S, Nijholt, D A T, Wong, T H, Rozemuller, A, Uitterlinden, A G, van Meurs, J G, van Swieten, J C & Netherlands Brain Bank 2019, ' Hippocampal transcriptome profiling combined with protein-protein interaction analysis elucidates Alzheimer's disease pathways and genes ', Neurobiology of Aging, vol. 74, pp. 225-233 . https://doi.org/10.1016/j.neurobiolaging.2018.10.023مصطلحات موضوعية: 0301 basic medicine, Male, Aging, Gene Expression, Computational biology, Disease, Biology, Hippocampal formation, Hippocampus, Protein–protein interaction, Transcriptome, 03 medical and health sciences, 0302 clinical medicine, Alzheimer Disease, Gene expression, Transcriptome profiling, Humans, Protein Interaction Maps, Gene, Aged, Aged, 80 and over, Sequence Analysis, RNA, General Neuroscience, Gene Expression Profiling, Middle Aged, 030104 developmental biology, RNA, Female, Neurology (clinical), Geriatrics and Gerontology, Signal transduction, 030217 neurology & neurosurgery, Developmental Biology, Signal Transduction
وصف الملف: application/pdf
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المؤلفون: Tsz Hang Wong
المصدر: De Neuroloog. 28:25-25
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0113261f6b3b1f132d0e8597523a8f4e
https://doi.org/10.24078/dng.2021.4.126717 -
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المؤلفون: John C. van Swieten, Giuseppe De Michele, Vincenzo Bonifati, Frank Jan de Jong, Guido J. Breedveld, Shamiram Melhem, Leonie J.M. Vergouw, Tsz Hang Wong, Chiara Criscuolo, Annemieke Ruitenberg, Marialuisa Quadri
المساهمون: Neurology, Clinical Genetics, Vergouw, L. J. M., Ruitenberg, A., Wong, T. H., Melhem, S., Breedveld, G. J., Criscuolo, C., De Michele, G., de Jong, F. J., Bonifati, V., van Swieten, J. C., Quadri, M.
المصدر: Parkinsonism & Related Disorders, 65, 243-247. Elsevier
مصطلحات موضوعية: Lewy Body Disease, Male, 0301 basic medicine, Parkinson's disease, Dementia with Lewy bodie, LRP10 gene, Disease, Parkinson's disease dementia, 03 medical and health sciences, Netherland, 0302 clinical medicine, mental disorders, Humans, LDL-Receptor Related Protein, Medicine, Dementia, Family history, Cognitive decline, LDL-Receptor Related Proteins, Exome sequencing, Netherlands, Aged, Genetics, Walcheren population, business.industry, Dementia with Lewy bodies, Haplotype, Parkinson Disease, Middle Aged, medicine.disease, 030104 developmental biology, Neurology, Female, Neurology (clinical), Geriatrics and Gerontology, business, 030217 neurology & neurosurgery, Human
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المؤلفون: Marc Hulsman, Sven J. van der Lee, Henne Holstege, Annemieke J.M. Rozemuller, Tsz Hang Wong, Cornelia M. van Duijn, Lieke H.H. Meeter, Harro Seelaar, M. Arfan Ikram, Petra Frick, Manuela Neumann, Jeroen J.M. Hoozemans, André G. Uitterlinden, Jeroen van Rooij, Rosa Rademakers, Shamiram Melhem, John C. van Swieten
المساهمون: Neurology, Pathology, Amsterdam Neuroscience - Neurodegeneration, Human genetics, Epidemiology, Internal Medicine
المصدر: Neurobiology of Aging: age-related phenomena, neurodegeneration and neuropathology, 73
Neurobiology of aging
Neurobiology of aging 73, 229.e11-229.e18 (2019). doi:10.1016/j.neurobiolaging.2018.08.016
Neurobiology of Aging, 73, 229.e11. Elsevier Inc.
Neurobiology of Aging, 73, 229.e11-229.e18. Elsevier Inc.
Neurobiology of Aging, 73:229.e11. Elsevier Inc.
Wong, T H, van der Lee, S J, van Rooij, J G J, Meeter, L H H, Frick, P, Melhem, S, Seelaar, H, Ikram, M A, Rozemuller, A J, Holstege, H, Hulsman, M, Uitterlinden, A, Neumann, M, Hoozemans, J J M, van Duijn, C M, Rademakers, R & van Swieten, J C 2019, ' EIF2AK3 variants in Dutch patients with Alzheimer's disease ', Neurobiology of Aging, vol. 73, pp. 229.e11-229.e18 . https://doi.org/10.1016/j.neurobiolaging.2018.08.016مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Exome sequencing, Aging, Candidate gene, genetics [Alzheimer Disease], metabolism [Hippocampus], Disease, Hippocampus, Whole Exome Sequencing, eIF-2 Kinase, Rotterdam Study, 0302 clinical medicine, Missing heritability problem, EIF2AK3, Non-U.S. Gov't, Exome, Netherlands, EIF2AK3 protein, human, General Neuroscience, Research Support, Non-U.S. Gov't, metabolism [eIF-2 Kinase], Middle Aged, Alzheimer's disease, genetics [Genetic Variation], eIF-2 Kinase/genetics, Genetic Variation/genetics, Female, Risk, PERK, medicine.medical_specialty, Neuroscience(all), Hippocampus/metabolism, Clinical Neurology, Research Support, 03 medical and health sciences, Alzheimer Disease, Internal medicine, medicine, Journal Article, Humans, ddc:610, Genotyping, Genetic Association Studies, Aged, Alzheimer Disease/genetics, genetics [eIF-2 Kinase], business.industry, Genetic Variation, Ageing, 030104 developmental biology, Neurology (clinical), Human medicine, Geriatrics and Gerontology, business, 030217 neurology & neurosurgery, Developmental Biology
وصف الملف: application/pdf; image/pdf; text/plain
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المؤلفون: Harro Seelaar, Annemieke J.M. Rozemuller, Tsz Hang Wong, Shamiram Melhem, John C. van Swieten
المساهمون: Neurology, Pathology, Amsterdam Neuroscience - Neurodegeneration
المصدر: Wong, T H, Seelaar, H, Melhem, S, Rozemuller, A J M & van Swieten, J C 2020, ' Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations ', Neurobiology of Aging, vol. 86, pp. 201.e9-201.e14 . https://doi.org/10.1016/j.neurobiolaging.2019.01.015
Neurobiology of Aging, 86. Elsevier Inc.
Neurobiology of Aging, 86, 201.e9-201.e14. Elsevier Inc.مصطلحات موضوعية: 0301 basic medicine, Male, Aging, medicine.disease_cause, Hippocampus, Presenilin, 03 medical and health sciences, Amyloid beta-Protein Precursor, 0302 clinical medicine, Alzheimer Disease, PSEN2, Presenilin-2, Amyloid precursor protein, PSEN1, Presenilin-1, Medicine, Humans, Early-onset Alzheimer's disease, Genetic Testing, Exome sequencing, Aged, Genetics, Aged, 80 and over, Cerebral Cortex, Mutation, biology, business.industry, General Neuroscience, medicine.disease, 030104 developmental biology, biology.protein, Female, Neurology (clinical), Geriatrics and Gerontology, business, 030217 neurology & neurosurgery, Developmental Biology, Frontotemporal dementia
وصف الملف: application/pdf
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المؤلفون: Annemieke J.M. Rozemuller, Harro Seelaar, Rick van Minkelen, David Hondius, Cyril Pottier, Lieke H.H. Meeter, John C. van Swieten, Shami Melhem, Jeroen van Rooij, Rosa Rademakers, Tsz Hang Wong, Cornelia M. van Duijn
المساهمون: Neurology, Internal Medicine, Clinical Genetics, Epidemiology, Netherlands Brain Bank, Netherlands Institute for Neuroscience (NIN), Pathology, Amsterdam Neuroscience - Neurodegeneration, Human genetics
المصدر: Wong, T H, Pottier, C, Hondius, D C, Meeter, L H H, van Rooij, J G J, Melhem, S, van Minkelen, R, van Duijn, C M, Rozemuller, A J M, Seelaar, H, Rademakers, R & van Swieten, J C 2018, ' Three VCP Mutations in Patients with Frontotemporal Dementia ', Journal of Alzheimer's Disease, vol. 65, no. 4, pp. 1139-1146 . https://doi.org/10.3233/JAD-180301
Journal of Alzheimers Disease, 65(4), 1139-1146. IOS Press BV
Journal of Alzheimer's disease
Journal of Alzheimer's Disease, 65, 1139-1146. IOS Press
Journal of Alzheimer's Disease, 65(4), 1139-1146. IOS Pressمصطلحات موضوعية: 0301 basic medicine, Male, Pathology, medicine.medical_specialty, Disease, medicine.disease_cause, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, C9orf72, Valosin Containing Protein, mental disorders, medicine, Humans, Genetic Testing, Amyotrophic lateral sclerosis, Pathological, Exome sequencing, Aged, Netherlands, Aged, 80 and over, Family Health, Neurologic Examination, Mutation, business.industry, General Neuroscience, Computational Biology, General Medicine, Frontotemporal lobar degeneration, Middle Aged, medicine.disease, DNA-Binding Proteins, Psychiatry and Mental health, Clinical Psychology, 030104 developmental biology, Frontotemporal Dementia, Female, Human medicine, Geriatrics and Gerontology, business, 030217 neurology & neurosurgery, Frontotemporal dementia
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe4a4391599a4343db9f262fdb21efbb
https://research.vumc.nl/en/publications/4bed0342-99c6-485a-94d5-8b874bb21bfd -
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المؤلفون: W.M. van der Flier, Patrizia Rizzu, Yolande A.L. Pijnenburg, Peter Heutink, Philip Scheltens, E. J. Meijers-Heijboer, Tsz Hang Wong, Frank Baas, Guido J. Breedveld, J. C. van Swieten, Petra E. Cohn-Hokke
المساهمون: Amsterdam Neuroscience, Genome Analysis, Cancer Center Amsterdam, Amsterdam Reproduction & Development (AR&D), Human Genetics, Human genetics, Neurology, NCA - neurodegeneration
المصدر: Journal of neurology, 261(11), 2085-2092. D. Steinkopff-Verlag
Cohn-Hokke, P E, Wong, T H, Rizzu, P, Breedveld, G, van der Flier, W M, Scheltens, P, Baas, F, Heutink, P, Meijers-Heijboer, E J, van Swieten, J C & Pijnenburg, Y A L 2014, ' Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort ', Journal of Neurology, vol. 261, no. 11, pp. 2085-2092 . https://doi.org/10.1007/s00415-014-7456-y
Journal of Neurology, 261(11), 2085-2092. D. Steinkopff-Verlagمصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, Neurology, medicine.disease_cause, Cohort Studies, C9orf72, Internal medicine, mental disorders, medicine, PSEN1, Humans, Dementia, Age of Onset, Mutation frequency, Aged, Netherlands, Genetics, Mutation, business.industry, Middle Aged, medicine.disease, Major gene, Cyclic AMP-Dependent Protein Kinase RIbeta Subunit, Female, Neurology (clinical), business, Frontotemporal dementia
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المؤلفون: Isabelle Le Ber, Agnès Camuzat, Véronique Golfier, John C. van Swieten, Serena Lattante, Serge Belliard, Alexis Brice, Bernard Laurent, Sophie Auriacombe, Stéphanie Millecamps, Bruno Dubois, Lena Guillot-Noel, Catherine Thomas-Antérion, Philippe Couratier, Tsz Hang Wong, Paola Caroppo, Fabienne Clot, Marc Teichmann
المساهمون: The Foundation 'Carlo Besta' Institute of Neurology ( IRCCS ), Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute ( ICM ), Centre National de la Recherche Scientifique ( CNRS ) -CHU Pitié-Salpêtrière [APHP]-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Université Pierre et Marie Curie - Paris 6 ( UPMC ), Laboratoire d'Etude des Mécanismes Cognitifs ( EMC ), Université Lumière - Lyon 2 ( UL2 ) -Centre National de la Recherche Scientifique ( CNRS ), Université Lumière - Lyon 2 ( UL2 ), Erasmus Medical Center Rotterdam, Fondazione IRCCS Istituto Neurologico 'Carlo Besta', Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute (ICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Laboratoire d'Etude des Mécanismes Cognitifs (EMC), Université Lumière - Lyon 2 (UL2), Erasmus University Medical Center [Rotterdam] (Erasmus MC), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Neurology
المصدر: Neurology: Genetics
Neurology: Genetics, 2016, 2 (3), pp. e80 〈10.1212/NXG.0000000000000080〉
Neurology Genetics
Neurology Genetics, American Academy of Neurology, 2016, 2 (3), pp. e80 ⟨10.1212/NXG.0000000000000080⟩
Neurology Genetics, 2016, 2 (3), pp. e80 ⟨10.1212/NXG.0000000000000080⟩
Neurology. Genetics, 2(3). Lippincott Williams & Wilkinsمصطلحات موضوعية: 0301 basic medicine, Proband, Genetic counseling, Settore MED/03 - GENETICA MEDICA, TARDBP, Article, 03 medical and health sciences, 0302 clinical medicine, mental disorders, Genotype, Medicine, Family history, frontotemporal dementias, Genetics (clinical), Genetics, [SDV.GEN]Life Sciences [q-bio]/Genetics, business.industry, medicine.disease, Penetrance, Phenotype, 3. Good health, 030104 developmental biology, Neurology (clinical), business, [ SDV.GEN ] Life Sciences [q-bio]/Genetics, 030217 neurology & neurosurgery, Frontotemporal dementia
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8142a0c4b18c6721e2083813a5a692db
https://hal.sorbonne-universite.fr/hal-01332741 -
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المؤلفون: Sven J. van der Lee, Rick van Minkelen, M. Arfan Ikram, Jeroen van Rooij, Lieke H.H. Meeter, André G. Uitterlinden, John C. van Swieten, Najaf Amin, Tsz Hang Wong, Cornelia M. van Duijn
المصدر: Alzheimer's & Dementia. 11
مصطلحات موضوعية: Genetics, Psychiatry and Mental health, Cellular and Molecular Neuroscience, Developmental Neuroscience, Epidemiology, business.industry, Health Policy, Medicine, Neurology (clinical), Disease, Geriatrics and Gerontology, business, Exome sequencing
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المؤلفون: Rutger W W Brouwer, Wiesje M. van der Flier, Seung Hoan Choi, Megan L. Grove, Edwin Oole, Sudha Seshadri, Tsz Hang Wong, Cornelia M. van Duijn, Thor Aspelund, Christopher J. O'Donnell, M. Arfan Ikram, Gudny Eirkisdottir, Jeroen van Rooij, Melissa E. Garcia, Johanna Jakobsdottir, Sven J. van der Lee, Anita L. DeStefano, Henne Holstege, Alexa S. Beiser, Wilfred F. J. van IJcken, Daniel Levy, Vilmundur Gudnason, Albert V. Smith, Mirjam C G N van den Hout, Albert Hofman, André G. Uitterlinden, John C. van Swieten, Yolande A.L. Pijnenburg, Bruce M. Psaty, Eric Boerwinkle, Najaf Amin, Lenore J. Launer, Joshua C. Bis, Valur Emilsson, Vincent Chouraki, Jerome I. Rotter, Philip Scheltens, Eva Louwersheimer
المساهمون: Human genetics, Neurology, NCA - neurodegeneration, Epidemiology, Internal Medicine, Cell biology
المصدر: Nature, 520(7545), E2-E3. Nature Publishing Group
van der Lee, S J, Holstege, H, Wong, T H, Jakobsdottir, J, Bis, J C, Chouraki, V, van Rooij, J G J, Grove, M L, Smith, A V, Amin, N, Choi, S H, Beiser, A S, Garcia, M E, van Ijcken, W F J, Pijnenburg, Y A L, Louwersheimer, E, Brouwer, R W W, van den Hout, M C G N, Oole, E, Eirkisdottir, G, Levy, D, Rotter, J I, Emilsson, V, O'Donnell, C J, Aspelund, T, Uitterlinden, A G, Launer, L J, Hofman, A, Boerwinkle, E, Psaty, B M, DeStefano, A L, Scheltens, P, Seshadri, S, van Swieten, J C, Gudnason, V, van der Flier, W M, Ikram, M A & van Duijn, C M 2015, ' PLD3 variants in population studies ', Nature, vol. 520, no. 7545, pp. E2-E3 . https://doi.org/10.1038/nature14038مصطلحات موضوعية: Genetics, Oncology, medicine.medical_specialty, education.field_of_study, Multidisciplinary, Confounding, Population, Odds ratio, Biology, Confidence interval, Article, Internal medicine, Genetic variation, Multiple comparisons problem, Cohort, medicine, education, Genetic association
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