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1Academic Journal
المؤلفون: Marian L. Hamshere, Peter A. Holmans, Dimitrios Avramopoulos, Susan S. Bassett, Deborah Blacker, Lars Bertram, Howard Wiener, Nan Rochberg, Rudolph E. Tanzi, A Myers, Fabienne Wavrant-de Vrièze, Rodney Go, Daniele Fallin, Simon Lovestone, John Hardy, Alison Goate, Julie Williams, Michael J. Owen
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.597.2470; http://hmg.oxfordjournals.org/content/16/22/2703.full.pdf
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2Academic Journal
المؤلفون: Yonghong Li, Andrew Grupe, Charles Rowl, Petra Nowotny, John S. K. Kauwe, Scott Smemo, Anthony Hinrichs, Kristina Tacey, Timothy A. Toombs, Shirley Kwok, Joseph Catanese, Thomas J. White, Taylor J. Maxwell, Paul Hollingworth, Richard Abraham, David C. Rubinsztein, Carol Brayne, Fabienne Wavrant-de Vrièze, John Hardy, Simon Lovestone, John C. Morris, Leon J. Thal, Michael Owen, Julie Williams, Alison Goate
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.567.7865; http://hmg.oxfordjournals.org/content/15/17/2560.full.pdf
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3
المؤلفون: Stephen S. Rich, Robert D. Brown, Mar Matarin, Javier Simón-Sánchez, Andrew B. Singleton, Angela Britton, Cynthia Crews, Scott Silliman, John Hardy, Dena G. Hernandez, Thomas G. Brott, Sonja W. Scholz, Bradford B. Worrall, J. Raphael Gibbs, Hon Chung Fung, Fabienne Wavrant-De Vrièze, James F. Meschia, L. Douglas Case
المصدر: Neurogenetics. 9:101-108
مصطلحات موضوعية: Male, medicine.medical_specialty, endocrine system diseases, Genomic Structural Variation, Gene Dosage, Genomics, Biology, Polymorphism, Single Nucleotide, White People, Article, Brain Ischemia, Cohort Studies, Cellular and Molecular Neuroscience, Risk Factors, Molecular genetics, mental disorders, Genetics, medicine, Humans, SNP, Copy-number variation, Genetics (clinical), Aged, Genetic association, Aged, 80 and over, Genome, Human, Middle Aged, Human genetics, Stroke, Case-Control Studies, North America, Female, Human genome
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4
المؤلفون: Fabienne Wavrant-De Vrièze, Ling Li, Meridith Womick, Jordi Pérez-Tur, Omanma Adighibe, Sampath Arepalli, Danielle Compton, John Hardy
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instnameمصطلحات موضوعية: Male, Linkage disequilibrium, Genotype, ABCA1, Locus (genetics), Chromosome 9, Disease, Biology, Article, Linkage Disequilibrium, Alzheimer Disease, Risk Factors, Genetic variation, medicine, Humans, Genetic Predisposition to Disease, Aged, Genetics, General Neuroscience, Haplotype, medicine.disease, Pedigree, Haplotypes, ATP-Binding Cassette Transporters, Female, lipids (amino acids, peptides, and proteins), Alzheimer's disease, Polymorphisms, Alzheimer’s disease, Polymorphism, Restriction Fragment Length, ATP Binding Cassette Transporter 1
وصف الملف: 66291 bytes; application/pdf
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5
المؤلفون: Kelly D. Foote, J. Raphael Gibbs, John Hardy, Jennifer C. Schymick, Carl D. Langefeld, Angela Britton, Fabienne Wavrant-De Vrièze, Sonja W. Scholz, Mar Matarin, Matt L Stiegert, Elizabeth Peckham, Michael S. Okun, Hubert H. Fernandez, Ronald J. Mandel, Ramon L. Rodriguez, Javier Simón-Sánchez, H.C. Fung, Dena G. Hernandez, Katrina Gwinn-Hardy, Andrew B. Singleton
المصدر: The Lancet Neurology. 5:911-916
مصطلحات موضوعية: Male, Parkinson's disease, Genotype, Single-nucleotide polymorphism, Disease, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Cohort Studies, Gene Frequency, Databases, Genetic, medicine, Humans, SNP, Genetic variability, International HapMap Project, Genotyping, Aged, Aged, 80 and over, Genetics, Chromosome Mapping, Parkinson Disease, Genomics, Middle Aged, medicine.disease, Female, Neurology (clinical)
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6
المؤلفون: Jaime Duckworth, Omanma Adighibe, Sampath Arepalli, Fabienne Wavrant-De Vrièze, John Hardy
المصدر: Neurobiology of Aging. 27:1431-1434
مصطلحات موضوعية: Male, Apolipoprotein E, Heterozygote, Aging, DNA Mutational Analysis, Receptors, Cytoplasmic and Nuclear, Locus (genetics), Disease, Biology, Bioinformatics, Risk Assessment, Apolipoproteins E, Alzheimer Disease, Risk Factors, Chromosome 19, Humans, Genetic Predisposition to Disease, Genetic Testing, Genetic variability, Allele, Liver X receptor, Gene, Aged, Liver X Receptors, Retrospective Studies, Aged, 80 and over, Chromosome Aberrations, Genetics, Polymorphism, Genetic, Incidence, General Neuroscience, Genetic Variation, Middle Aged, Orphan Nuclear Receptors, United States, Female, Neurology (clinical), Geriatrics and Gerontology, Chromosomes, Human, Pair 19, Developmental Biology
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7
المؤلفون: Michael John Owen, John J. Sninsky, Michael Conlon O'Donovan, Anthony L. Hinrichs, Sara Cherny, Ryan van Luchene, John Powell, Yonghong Li, Catherine Foy, John Hardy, Fabienne Wavrant-De Vrièze, Taylor J. Maxwell, Petra Nowotny, Lisa Doil, Peter Holmans, Leon J. Thal, Simon Lovestone, Nicola Archer, Christopher Morris, John C. Morris, Charles M. Rowland, Scott Smemo, Alison Goate, Joseph J. Catanese, Luke Jehu, Julie Williams, Lesley Jones, John S. K. Kauwe, Paul Hollingworth, Gillian Hamilton, Mona Kaleem, Amanda J. Myers, Kristina Tacey, Andrew Grupe, Thomas J. White
المصدر: The American Journal of Human Genetics. 78:78-88
مصطلحات موضوعية: Genetics, 0303 health sciences, education.field_of_study, Candidate gene, Population, Haplotype, Single-nucleotide polymorphism, Locus (genetics), Articles, Biology, 03 medical and health sciences, 0302 clinical medicine, Genetic marker, Genetic linkage, Genetics(clinical), Allele, education, 030217 neurology & neurosurgery, Genetics (clinical), 030304 developmental biology
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8
المؤلفون: Jordi Pérez-Tur, Tuomo Polvikoski, Dena G. Hernandez, Pentti J. Tienari, Karoliina Reunanen, Fabienne Wavrant-De Vrièze, Clare Ellis, Irma-Leena Notkola, John Hardy, Raimo Sulkava, Kimmo Kontula, Auli Verkkoniemi, Matti Haltia, Liisa Myllykangas
المصدر: American Journal of Medical Genetics. 114:288-291
مصطلحات موضوعية: Apolipoprotein E, medicine.medical_specialty, Genotype, Population, Apolipoprotein E3, Neuropathology, Biology, Genetic determinism, 03 medical and health sciences, Apolipoproteins E, 0302 clinical medicine, Degenerative disease, Alzheimer Disease, Internal medicine, mental disorders, medicine, Humans, Allele, Promoter Regions, Genetic, education, Genetics (clinical), Aged, 030304 developmental biology, Aged, 80 and over, Genetics, 0303 health sciences, education.field_of_study, Amyloid beta-Peptides, Polymorphism, Genetic, Haplotype, Brain, medicine.disease, Endocrinology, Haplotypes, lipids (amino acids, peptides, and proteins), Alzheimer's disease, 030217 neurology & neurosurgery
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9
المؤلفون: Joyce van de Leemput, Henry Houlden, Ian Rafferty, Andrew B. Singleton, Fabienne Wavrant-De Vrièze, John Hardy, Paola Giunti, Jose Bras, Elizabeth M. C. Fisher
المصدر: Movement Disorders. 25:771-773
مصطلحات موضوعية: Adult, Male, Ataxia, Adolescent, Locus (genetics), Biology, Article, Cohort Studies, Young Adult, Exon, medicine, Humans, Inositol 1,4,5-Trisphosphate Receptors, Point Mutation, Spinocerebellar Ataxias, Missense mutation, Coding region, Gene, Genetics, Point mutation, Exons, Sequence Analysis, DNA, Middle Aged, medicine.disease, Neurology, Spinocerebellar ataxia, Female, Neurology (clinical), medicine.symptom
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10
المؤلفون: John Hardy, Luc Defebvre, Marie-Christine Chartier-Harlin, Sarah Lincoln, Fabienne Wavrant-De Vrièze, Matthew J. Farrer, Florence Richard, Alain Destée, Vincent Mouroux, Philippe Amouyel, Estelle Becquet
المصدر: Movement Disorders. 15:1075-1083
مصطلحات موضوعية: Genetics, Neurology, Genetic linkage, Genetic heterogeneity, Genetic marker, Haplotype, Locus (genetics), Neurology (clinical), Biology, Age of onset, Genetic determinism, Parkin
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::11092fbb9e7941a421bcd006c03f7367
https://doi.org/10.1002/1531-8257(200011)15:6<1075::aid-mds1004>3.0.co;2-2 -
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المؤلفون: Nigel Williams, Dzanan Ramic, Jordi Pérez-Tur, William Wu, Patrick G. Kehoe, Hywel Williams, I. Fenton, Richard Crook, Kimberly A. Roehl, Shantia Shears, Marie-Christine Chartier-Harlin, Gillian Spurlock, Michael John Owen, Peter Holmans, Julie Williams, Alison Goate, John Hardy, Mike Hutton, Nadine Norton, Jeremy Booth, Wendy Van Voorst, Fabienne Wavrant-De Vrièze, Simon Lovestone
المصدر: University of Bristol-PURE
مصطلحات موضوعية: Male, Population, Genome Scan, chemical and pharmacologic phenomena, Locus (genetics), Biology, Apolipoproteins E, Gene mapping, Alzheimer Disease, Genetics, Humans, Genetic Predisposition to Disease, Age of Onset, Allele, education, Molecular Biology, Alleles, Genetics (clinical), Genetic association, Family Health, education.field_of_study, Genome, Human, Chromosome Mapping, Chromosome, DNA, General Medicine, Microsatellite, Female, Lod Score
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12
المؤلفون: John Hardy, Julie Williams, Elin S. Blom, Anna Glaser, Omanma Adighibe, Lars Lannfelt, Alison Goate, Sampath Arepalli, Marian L. Hamshere, Fabienne Wavrant-De Vrièze, Vilmantas Giedraitis
المصدر: BMC Medical Genetics, Vol 10, Iss 1, p 122 (2009)
BMC Medical Geneticsمصطلحات موضوعية: Apolipoprotein E, lcsh:Internal medicine, lcsh:QH426-470, Genetic Linkage, Genome-wide association study, Biology, 03 medical and health sciences, Apolipoproteins E, 0302 clinical medicine, Alzheimer Disease, Genetic linkage, Research article, Genetics, medicine, Humans, Genetic Predisposition to Disease, Genetics(clinical), Allele, lcsh:RC31-1245, Gene, Genetics (clinical), Aged, 030304 developmental biology, Aged, 80 and over, Linkage (software), 0303 health sciences, Middle Aged, medicine.disease, R1, United Kingdom, United States, Human genetics, lcsh:Genetics, Alzheimer's disease, 030217 neurology & neurosurgery, Genome-Wide Association Study, Microsatellite Repeats
وصف الملف: application/pdf
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13
المؤلفون: Hernandez Dena, E. Jeffrey Metter, John Hardy, James F. Meschia, Luigi Ferruci, L. Douglas Case, Dale M Gamble, Thomas G. Brott, Mar Matarin, Stephen J. Chanock, Robert D. Brown, Andrew B. Singleton, Bradford B. Worrall, W. Mark Brown, Stephen S. Rich, Angela Britton, Fabienne Wavrant-De Vrièze
المصدر: Stroke. 40(11)
مصطلحات موضوعية: Genetic Markers, Male, Pathology, medicine.medical_specialty, Candidate gene, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Article, Brain Ischemia, Polymorphism (computer science), Genotype, Medicine, Humans, Allele, Stroke, Aged, Advanced and Specialized Nursing, Genetics, Aged, 80 and over, business.industry, Case-control study, Middle Aged, medicine.disease, Case-Control Studies, Cohort, Female, Neurology (clinical), Cardiology and Cardiovascular Medicine, business
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14Academic Journal
المؤلفون: James F. Meschia, Sampath Arepalli, Fabienne Wavrant-de Vrièze, Jaime Duckworth, Andrew B. Singleton, Bradford B. Worrall, Thomas G. Brott, Robert D. Brown, W. Mark Brown, Stephen S. Rich, Ma Stephen, S. Rich, Phd Sampath Arepalli, Fabienne Wavrant-de Vrièze, Phd Jaime Duckworth, Ms Andrew, B. Singleton
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.571.3871; http://stroke.ahajournals.org/content/38/4/1189.full.pdf
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15
المؤلفون: James F. Meschia, Bradford B. Worrall, Stephen S. Rich, Andrew B. Singleton, W. Mark Brown, John Hardy, Jaime Duckworth, Sampath Arepalli, Thomas G. Brott, Fabienne Wavrant-De Vrièze, Robert D. Brown
المصدر: Stroke. 38(4)
مصطلحات موضوعية: Male, medicine.medical_specialty, DNA Mutational Analysis, Ischemia, Minisatellite Repeats, White People, Article, Brain Ischemia, Brain ischemia, Cohort Studies, Gene Frequency, Internal medicine, Genotype, Medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Stroke, Allele frequency, Aged, Advanced and Specialized Nursing, Inflammation, Polymorphism, Genetic, business.industry, Siblings, Odds ratio, Middle Aged, medicine.disease, Surgery, Variable number tandem repeat, Interleukin 1 Receptor Antagonist Protein, North America, Female, Neurology (clinical), Cardiology and Cardiovascular Medicine, business, Cohort study
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16
المؤلفون: Andrew B. Singleton, Josephine M. Egan, Beatriz L. Rodriguez, Ilija Kovac, Daniel J. Foley, J. David Curb, Kamal Masaki, Richard J. Havlik, Dena G. Hernandez, Alexander F. Wilson, Rita Peila, Fabienne Wavrant-De Vrièze, Dennis D. Taub, Wilfred Y. Fujimoto
مصطلحات موضوعية: Genetic Markers, Male, medicine.medical_specialty, Genotype, Genetic Linkage, Endocrinology, Diabetes and Metabolism, Type 2 diabetes, Biology, Article, Hawaii, Japan, Genetic linkage, Internal medicine, Diabetes mellitus, Glucose Intolerance, Internal Medicine, medicine, Glucose homeostasis, Humans, Aged, 80 and over, Chromosomes, Human, Pair 14, Adiponectin, medicine.disease, Obesity, Exact test, Endocrinology, Phenotype, Genetic epidemiology, Diabetes Mellitus, Type 2, Chromosomes, Human, Pair 1, Monte Carlo Method, Microsatellite Repeats
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17
المؤلفون: Fabienne Wavrant-De Vrièze, Adrian M. Isaacs, Matt Baker, Mike Hutton
المصدر: Genomics. 51:152-154
مصطلحات موضوعية: Genetics, Polymorphism, Genetic, Parkinsonism, Parkinson Disease, Exons, Biology, medicine.disease, Introns, Temporal Lobe, Frontal Lobe, Chromosome 17 (human), Exon, Glial Fibrillary Acidic Protein, Mutation, medicine, Humans, Dementia, Coding region, Alzheimer's disease, Gene, Alleles, Chromosomes, Human, Pair 17, Frontotemporal dementia
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18
المؤلفون: Judith C. Keen, Josefina Nash, Fabienne Wavrant-De Vrièze, John Hardy, H.C. Fung, Andrew B. Singleton, Javier Simón-Sánchez, Mar Matarin, Dena G. Hernandez, Sonja W. Scholz, Katrina Gwinn-Hardy, Angela Britton, J. Raphael Gibbs, Digamber Borgaonkar, Anthony Crawley, Elizabeth Peckham
المصدر: Human molecular genetics. 16(1)
مصطلحات موضوعية: Genotype, Population, Genomics, Single-nucleotide polymorphism, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Cohort Studies, Gene Frequency, Computer Systems, Genetic variation, Genetics, Humans, Genetic variability, International HapMap Project, education, Molecular Biology, Allele frequency, Genetics (clinical), Aged, Cell Line, Transformed, Aged, 80 and over, Chromosome Aberrations, education.field_of_study, Genome, Human, Homozygote, Genetic Variation, General Medicine, DNA, Middle Aged, SNP array
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19
المؤلفون: Fabienne Wavrant-De Vrièze, Sandro Sorbi, Hsinhwa Lee, John Hardy, Derek Gordon, Silvia Bagnoli, Abraham M. Brown, Elena Cellini, John P. Blass, Benedetta Nacmias
المصدر: Neurochemical research. 32(4-5)
مصطلحات موضوعية: Male, Linkage disequilibrium, Genotype, Genetic Linkage, Population, Single-nucleotide polymorphism, Locus (genetics), Biology, Biochemistry, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Cohort Studies, Cellular and Molecular Neuroscience, Gene Frequency, Genetic linkage, Alzheimer Disease, Genetic model, Humans, education, Allele frequency, Alleles, Aged, Dihydrolipoamide Dehydrogenase, Genetics, education.field_of_study, General Medicine, United States, Logistic Models, Italy, Case-Control Studies, Jews, Chromosomal region, Female, Algorithms, Chromosomes, Human, Pair 7
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20
المؤلفون: Shirley Kwok, Thomas J. White, John S. K. Kauwe, Carol Brayne, Yonghong Li, Petra Nowotny, Fabienne Wavrant-De Vrièze, David C. Rubinsztein, Michael Conlon O'Donovan, Timothy A. Toombs, Simon Lovestone, Kristina Tacey, Alison Goate, Anthony L. Hinrichs, Scott Smemo, Paul Hollingworth, John C. Morris, Joseph J. Catanese, Andrew Grupe, Julie Williams, Richard Abraham, Charles M. Rowland, Taylor J. Maxwell, Leon J. Thal, John Hardy, Michael John Owen
المصدر: Human molecular genetics. 15(17)
مصطلحات موضوعية: Genetic Markers, Male, Linkage disequilibrium, Genetic Linkage, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Gene Frequency, Alzheimer Disease, Genetics, SNP, Humans, Genetic Predisposition to Disease, Allele, Molecular Biology, Allele frequency, Genetics (clinical), Alleles, Genetic association, Binding Sites, General Medicine, Minor allele frequency, Death-Associated Protein Kinases, Genetic marker, Case-Control Studies, Calcium-Calmodulin-Dependent Protein Kinases, Female, Apoptosis Regulatory Proteins, Chromosomes, Human, Pair 9, Databases, Nucleic Acid