Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kin Ying Mok"'
Autor:
Nor Azian Abdul Murad, Siti Aishah Sulaiman, Azlina Ahmad-Annuar, Norlinah Mohamed Ibrahim, Wael Mohamed, Shahrul Azmin Md Rani, Kin Ying Mok
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Externí odkaz:
https://doaj.org/article/6291a55ab95c40549b9884a84fc4249c
Autor:
Artur Francisco, Schumacher-Schuh, Andrei, Bieger, Olaitan, Okunoye, Kin Ying, Mok, Shen-Yang, Lim, Soraya, Bardien, Azlina, Ahmad-Annuar, Bruno Lopes, Santos-Lobato, Matheus Zschornack, Strelow, Mohamed, Salama, Shilpa C, Rao, Yared Zenebe, Zewde, Saiesha, Dindayal, Jihan, Azar, Lingappa Kukkle, Prashanth, Roopa, Rajan, Alastair J, Noyce, Njideka, Okubadejo, Mie, Rizig, Suzanne, Lesage, Ignacio Fernandez, Mata, Masharip, Atadzhanov
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 37(8)
Human genetics research lacks diversity; over 80% of genome-wide association studies have been conducted on individuals of European ancestry. In addition to limiting insights regarding disease mechanisms, disproportionate representation can create di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e4c3cc1152ff680c8c1bcf74dcab08a
https://pubmed.ncbi.nlm.nih.gov/35867623
https://pubmed.ncbi.nlm.nih.gov/35867623
Autor:
Abdul Murad, Nor Azian, Sulaiman, Siti Aishah, Ahmad-Annuar, Azlina, Ibrahim, Norlinah Mohamed, Mohamed, Wael, Md Rani, Shahrul Azmin, Kin Ying Mok
Publikováno v:
Frontiers in Aging Neuroscience; 12/16/2022, Vol. 14, p1-4, 4p
Autor:
Kin Ying Mok
Publikováno v:
JAMA Network Open
Key Points Question What are the associations between the Alzheimer disease risk allele apolipoprotein E (APOE) ε4 and attention across the life span of individuals with Down syndrome? Findings In a cross-sectional study including 80 young children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e7b8b660c3e189e95c2c8f5f23c420a
https://pubmed.ncbi.nlm.nih.gov/32986108
https://pubmed.ncbi.nlm.nih.gov/32986108
Autor:
Leonardo Collado-Torres, Oluwadamilola Ojo, Huw Morris, Andy Thomason, Isabel Gonzalez-Aramburu, Mie Rizig, Sara Bandrés Ciga, Patrick Lewis, María Teresa Periñán, Pau Pastor, Nicholas Wood, Kerrin Small, John Quinn, PAOLA FORABOSCO, Rubén Fernández-Santiago, Astrid Daniela Adarmes Gómez, Juan Carlos Martinez Castrillo, Sonja Scholz, Victoria Alvarez, Niccolò Emanuele Mencacci, Michael Weale, Thomas Gasser, Kari Majamaa, Adolfo Mínguez-Castellanos, Jose Bras, J. Raphael Gibbs, Monica Diez-Fairen, Ruth Lovering, Jon Infante, Juan A. Botía, Rita Guerreiro, John Hardy, Mario Ezquerra, Valentina Escott-Price, Arianna Tucci, Kin Ying Mok, Kerri J Kinghorn, Manuel Menéndez González, Janet Hoenicka, Njideka Okubadejo, Regina Reynolds, Alexis Brice, Ignacio Alvarez, Adaikalavan Ramasamy, Pille Taba, David Zhang, Lydia Vela-Desojo
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Guelfi, S, D’sa, K, Botía, J A, Vandrovcova, J, Reynolds, R H, Zhang, D, Trabzuni, D, Collado-torres, L, Thomason, A, Quijada Leyton, P, Gagliano Taliun, S A, Nalls, M A, Small, K S, Smith, C, Ramasamy, A, Hardy, J, Weale, M E & Ryten, M 2020, ' Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information ', Nature Communications, vol. 11, no. 1 . https://doi.org/10.1038/s41467-020-14483-x
Nature communications, vol 11, iss 1
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications 11, 1041 (2020).
UCrea Repositorio Abierto de la Universidad de Cantabria
Nature communications
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Guelfi, S, D’sa, K, Botía, J A, Vandrovcova, J, Reynolds, R H, Zhang, D, Trabzuni, D, Collado-torres, L, Thomason, A, Quijada Leyton, P, Gagliano Taliun, S A, Nalls, M A, Small, K S, Smith, C, Ramasamy, A, Hardy, J, Weale, M E & Ryten, M 2020, ' Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information ', Nature Communications, vol. 11, no. 1 . https://doi.org/10.1038/s41467-020-14483-x
Nature communications, vol 11, iss 1
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications 11, 1041 (2020).
UCrea Repositorio Abierto de la Universidad de Cantabria
Nature communications
International Parkinson’s Disease Genomics Consortium (IPDGC), UK Brain Expression Consortium (UKBEC).
Genome-wide association studies have generated an increasing number of common genetic variants associated with neurological and psychiatric
Genome-wide association studies have generated an increasing number of common genetic variants associated with neurological and psychiatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::983ce5373a8661d389b6fcfe05e9de4f
https://doi.org/10.1038/s41467-020-14483-x
https://doi.org/10.1038/s41467-020-14483-x
Autor:
Cristina Tejera-Parrado, Jean-christophe Corvol, Huw Morris, Rauan Kaiyrzhanov, Sebastian Schreglmann, Mie Rizig, Sara Bandrés Ciga, Francisco Javier Barrero Hernández, Patrick Lewis, Nicholas Wood, Claudia Schulte, John Quinn, Astrid Daniela Adarmes Gómez, Juan Carlos Martinez Castrillo, Berta María Pascual Sedano, Victoria Alvarez, Niccolò Emanuele Mencacci, Thomas Gasser, Ziv Gan-Or, Luis Bonet-Ponce, Adolfo Mínguez-Castellanos, Jose Bras, J. Raphael Gibbs, Monica Diez-Fairen, Viorica Chelban, Ruth Lovering, Jon Infante, Oriol Dols Icardo, Hirotaka Iwaki, Rita Guerreiro, John Hardy, Mario Ezquerra, Kin Ying Mok, Kerri J Kinghorn, Beatriz De la Casa-Fages, Peter Heutink, Manuel Menéndez González, Francisco Escamilla Sevilla, Sara Saez-Atienzar, Alexis Brice, Ignacio Alvarez, Pille Taba
Publikováno v:
Movement
Movement disorders : official journal of the Movement Disorder Society, vol 34, iss 4
Movement disorders : official journal of the Movement Disorder Society, vol 34, iss 4
Background PD is a complex polygenic disorder. In recent years, several genes from the endocytic membrane-trafficking pathway have been suggested to contribute to disease etiology. However, a systematic analysis of pathway-specific genetic risk facto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc57b205c12177e309814c86ba6bcec
http://livrepository.liverpool.ac.uk/3031818/1/Bandres-Ciga_et_al-2019-Movement_Disorders.pdf
http://livrepository.liverpool.ac.uk/3031818/1/Bandres-Ciga_et_al-2019-Movement_Disorders.pdf
Autor:
Daniel Alexander, Andre Strydom, Elizabeth Fisher, Carla Startin, Sarah Hamburg, Peter Wijeratne, Rosalyn Hithersay, John Hardy, Kin Ying Mok, Nicholas Firth
Publikováno v:
Annals of clinical and translational neurology. 5(6)
Objective Individuals with Down syndrome (DS) have an extremely high genetic risk for Alzheimer's disease (AD), however, the course of cognitive decline associated with progression to dementia is ill-defined. Data-driven methods can estimate long-ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83c652ce41057cc021a388c3c30a586d
https://pubmed.ncbi.nlm.nih.gov/29928657
https://pubmed.ncbi.nlm.nih.gov/29928657
Autor:
Kin Ying Mok
Publikováno v:
The Lancet Neurology. 9:1145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::374b777a818259be1a0d693cd170b337
https://doi.org/10.1016/s1474-4422(10)70252-0
https://doi.org/10.1016/s1474-4422(10)70252-0