المؤلفون: Hermes S; Parabon NanoLabs, Inc., Reston, VA, USA., Cady J; Parabon NanoLabs, Inc., Reston, VA, USA., Armentrout S; Parabon NanoLabs, Inc., Reston, VA, USA., O'Connor J; Parabon NanoLabs, Inc., Reston, VA, USA., Holdaway SC; Parabon NanoLabs, Inc., Reston, VA, USA., Cruchaga C; Department of Psychiatry, Washington University, St. Louis, MO, USA.; Hope Center Program on Protein Aggregation and Neurodegeneration, Washington University, St. Louis, MO, USA., Wingo T; Goizueta Alzheimer's Disease Center, Emory University School of Medicine, Atlanta, GA, USA.; Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA., Greytak EM; Parabon NanoLabs, Inc., Reston, VA, USA.

مؤلفون مشاركون: the Alzheimer’s Disease Neuroimaging Initiative

المصدر: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2024; Vol. 99 (4), pp. 1425-1440.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9814863 Publication Model: Print Cited Medium: Internet ISSN: 1875-8908 (Electronic) Linking ISSN: 13872877 NLM ISO Abbreviation: J Alzheimers Dis Subsets: MEDLINE

مواضيع طبية MeSH: Alzheimer Disease*/genetics , Machine Learning* , Multifactorial Inheritance*/genetics , Epistasis, Genetic*/genetics , Genetic Predisposition to Disease*/genetics, Humans ; Female ; Male ; Polymorphism, Single Nucleotide/genetics ; Aged ; Genome-Wide Association Study/methods ; Apolipoproteins E/genetics ; Models, Genetic ; Genetic Risk Score

المؤلفون: Cetinsoy O; Biosciences, Clifton Campus, Nottingham Trent University, Nottingham, UK., Anyanwu I; Biosciences, Clifton Campus, Nottingham Trent University, Nottingham, UK., Krishnanand H; Biosciences, Clifton Campus, Nottingham Trent University, Nottingham, UK., Natarajan G; Biosciences, Clifton Campus, Nottingham Trent University, Nottingham, UK., Ramachandran N; Biosciences, Clifton Campus, Nottingham Trent University, Nottingham, UK., Thomas A; Brains for Dementia Research, Faculty of Medical Sciences, Newcastle University, Newcastle, UK., Brookes KJ; Biosciences, Clifton Campus, Nottingham Trent University, Nottingham, UK.

المصدر: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2024; Vol. 99 (1), pp. 241-250.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9814863 Publication Model: Print Cited Medium: Internet ISSN: 1875-8908 (Electronic) Linking ISSN: 13872877 NLM ISO Abbreviation: J Alzheimers Dis Subsets: MEDLINE

مواضيع طبية MeSH: Alzheimer Disease*/genetics , Genetic Association Studies* , Genetic Predisposition to Disease*/genetics , Polymorphism, Single Nucleotide*/genetics , Receptors, Urokinase Plasminogen Activator*/genetics , Urokinase-Type Plasminogen Activator*/genetics, Aged ; Aged, 80 and over ; Female ; Humans ; Male ; Cohort Studies ; Genotype

المؤلفون: Zou L; Department of Obstetrics and Gynecology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China., Dong W; Department of Obstetrics and Gynecology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China., Ai Y; Department of Obstetrics and Gynecology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China., Li Y; Department of Obstetrics and Gynecology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China., Cheng Y; Department of Obstetrics and Gynecology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China., Feng Y; Department of Obstetrics and Gynecology, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.; The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.

المصدر: Technology and health care : official journal of the European Society for Engineering and Medicine [Technol Health Care] 2024; Vol. 32 (3), pp. 1871-1879.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9314590 Publication Model: Print Cited Medium: Internet ISSN: 1878-7401 (Electronic) Linking ISSN: 09287329 NLM ISO Abbreviation: Technol Health Care Subsets: MEDLINE

مواضيع طبية MeSH: Nitric Oxide Synthase Type III*/genetics , Abortion, Habitual*/genetics , Genetic Predisposition to Disease*, Humans ; Female ; China/epidemiology ; Adult ; Pregnancy ; Polymorphism, Single Nucleotide ; Minisatellite Repeats/genetics ; Polymorphism, Genetic

المؤلفون: Lim SY; The Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, University of Malaya, Kuala Lumpur, Malaysia.; Department of Medicine, Faculty of Medicine, Division of Neurology, University of Malaya, Kuala Lumpur, Malaysia., Klein C; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.

المصدر: Journal of Parkinson's disease [J Parkinsons Dis] 2024; Vol. 14 (3), pp. 467-482.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 101567362 Publication Model: Print Cited Medium: Internet ISSN: 1877-718X (Electronic) Linking ISSN: 18777171 NLM ISO Abbreviation: J Parkinsons Dis Subsets: MEDLINE

مواضيع طبية MeSH: Parkinson Disease*/genetics , Glucosylceramidase*/genetics , Leucine-Rich Repeat Serine-Threonine Protein Kinase-2*/genetics , alpha-Synuclein*/genetics , Genetic Predisposition to Disease*, Humans

المؤلفون: Luaibi HA, Mohammed BJ

المصدر: Human antibodies [Hum Antibodies] 2024; Vol. 32 (2), pp. 67-74.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9711270 Publication Model: Print Cited Medium: Internet ISSN: 1875-869X (Electronic) Linking ISSN: 10932607 NLM ISO Abbreviation: Hum Antibodies Subsets: MEDLINE

مواضيع طبية MeSH: beta-Thalassemia*/genetics , Tumor Necrosis Factor-alpha*/genetics , Genotype* , Liver Diseases*/genetics , Pancreatic Diseases*/genetics, Humans ; Adult ; Male ; Female ; Iraq ; Polymorphism, Single Nucleotide/genetics ; Young Adult ; Case-Control Studies ; Gene Frequency ; Gene Expression/genetics ; Adolescent ; Genetic Predisposition to Disease ; Alleles

المؤلفون: Reyes-Pérez P; Laboratorio Internacional de Investigación Sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, México., García-Marín LM; Laboratorio Internacional de Investigación Sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, México.; Mental Health and Neuroscience Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.; School of Biomedical Sciences, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia., Aman AM; Mental Health and Neuroscience Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.; School of Biomedical Sciences, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia., Antar T; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA., Flores-Ocampo V; Laboratorio Internacional de Investigación Sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, México.; Licenciatura en Ciencias Genómicas, Escuela Nacional de Estudios Superiores Unidad Juriquilla, Universidad Nacional Autónoma de México, Querétaro, México., Mitchell BL; Mental Health and Neuroscience Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia., Medina-Rivera A; Laboratorio Internacional de Investigación Sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, México., Rentería ME; Mental Health and Neuroscience Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.; School of Biomedical Sciences, Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.; School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD,Australia.

المصدر: Journal of Parkinson's disease [J Parkinsons Dis] 2024; Vol. 14 (3), pp. 483-493.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 101567362 Publication Model: Print Cited Medium: Internet ISSN: 1877-718X (Electronic) Linking ISSN: 18777171 NLM ISO Abbreviation: J Parkinsons Dis Subsets: MEDLINE

مواضيع طبية MeSH: Parkinson Disease*/genetics , Genome-Wide Association Study* , Depression*/genetics , Depression*/etiology , Mendelian Randomization Analysis*, Humans ; Genetic Predisposition to Disease ; Linkage Disequilibrium ; Polymorphism, Single Nucleotide

المؤلفون: Khaled M, Al-Jamal H; Faculty of Public Health III, Lebanese University, Tripoli, Lebanon., Tajer L; Faculty of Public Health III, Lebanese University, Tripoli, Lebanon., El-Mir R; Faculty of Public Health III, Lebanese University, Tripoli, Lebanon.

المصدر: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2024; Vol. 99 (1), pp. 21-40.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9814863 Publication Model: Print Cited Medium: Internet ISSN: 1875-8908 (Electronic) Linking ISSN: 13872877 NLM ISO Abbreviation: J Alzheimers Dis Subsets: MEDLINE

مواضيع طبية MeSH: Alzheimer Disease*/genetics , Alzheimer Disease*/epidemiology, Humans ; Lebanon/epidemiology ; Risk Factors ; Genetic Predisposition to Disease/genetics

المؤلفون: Lafi And ZK, Mohammed BJ

المصدر: Human antibodies [Hum Antibodies] 2024; Vol. 32 (1), pp. 1-8.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9711270 Publication Model: Print Cited Medium: Internet ISSN: 1875-869X (Electronic) Linking ISSN: 10932607 NLM ISO Abbreviation: Hum Antibodies Subsets: MEDLINE

مواضيع طبية MeSH: Receptors, Calcitriol*/genetics , Multiple Sclerosis*/genetics, Male ; Humans ; Female ; Young Adult ; Adult ; Middle Aged ; Interleukin-18/genetics ; Iraq ; Genetic Predisposition to Disease/genetics ; Polymorphism, Single Nucleotide/genetics ; Genotype ; Gene Frequency/genetics ; Case-Control Studies ; Gene Expression/genetics ; Vitamin D

المؤلفون: Li Y; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China.; Department Five of Neurology, Cangzhou Central Hospital, Yunhe District, Cangzhou, Hebei, China., Yang Z; College of Life Sciences, University of Chinese Academy of Sciences, Shijingshan District, Beijing, China.; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China., Zhang Y; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China., Liu F; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China., Xu J; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China., Meng Y; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China., Xing G; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China., Ruan X; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China., Sun J; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China., Zhang N; Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Heping District, Tianjin, China.

المصدر: Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2024; Vol. 99 (2), pp. 577-593.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9814863 Publication Model: Print Cited Medium: Internet ISSN: 1875-8908 (Electronic) Linking ISSN: 13872877 NLM ISO Abbreviation: J Alzheimers Dis Subsets: MEDLINE

مواضيع طبية MeSH: Alzheimer Disease*/genetics , Frontotemporal Lobar Degeneration*/genetics , Genetic Testing*/methods , Asian People*/genetics, Humans ; Male ; Female ; Aged ; Middle Aged ; Exome Sequencing ; China/epidemiology ; C9orf72 Protein/genetics ; Aged, 80 and over ; Genetic Predisposition to Disease/genetics ; East Asian People

المؤلفون: Welton T; National Neuroscience Institute, Singapore.; Duke-NUS Medical School, Singapore., Teo TWJ; National Neuroscience Institute, Singapore., Chan LL; National Neuroscience Institute, Singapore.; Duke-NUS Medical School, Singapore.; Department of Diagnostic Radiology, Singapore General Hospital, Singapore., Tan EK; National Neuroscience Institute, Singapore.; Duke-NUS Medical School, Singapore.; Department of Neurology, Singapore General Hospital, Singapore., Tan LCS; National Neuroscience Institute, Singapore.; Duke-NUS Medical School, Singapore.

المصدر: Journal of Parkinson's disease [J Parkinsons Dis] 2024; Vol. 14 (4), pp. 713-724.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: IOS Press Country of Publication: Netherlands NLM ID: 101567362 Publication Model: Print Cited Medium: Internet ISSN: 1877-718X (Electronic) Linking ISSN: 18777171 NLM ISO Abbreviation: J Parkinsons Dis Subsets: MEDLINE

مواضيع طبية MeSH: Parkinson Disease*/genetics , Parkinson Disease*/pathology , Parkinson Disease*/physiopathology , Parkinson Disease*/diagnostic imaging , White Matter*/diagnostic imaging , White Matter*/pathology, Humans ; Female ; Male ; Aged ; Middle Aged ; Magnetic Resonance Imaging ; Genome-Wide Association Study ; Brain/pathology ; Brain/diagnostic imaging ; Polymorphism, Single Nucleotide ; Genetic Predisposition to Disease ; Gray Matter/diagnostic imaging ; Gray Matter/pathology ; Asian People/genetics