نتائج البحث - Kristin Levine
- يعرض 1 - 17 نتائج من 17
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omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases حسب Chelsea X. Alvarado, Mary B. Makarious, Cory A. Weller, Dan Vitale, Mathew J. Koretsky, Sara Bandrés‐Ciga, Hirotaka Iwaki, Kristin Levine, Andrew Singleton, Faraz Faghri, Mike A. Nalls, Hampton L. Leonard
منشور في 2024Artigo -
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Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature حسب Caroline Jonson, Kristin Levine, Julie Lake, Linnea Hertslet, Lietsel Jones, Dhairya Patel, Jeff Kim, Sara Bandrés‐Ciga, Nancy Terry, Ignácio F. Mata, Cornelis Blauwendraat, Andrew Singleton, Mike A. Nalls, Jennifer S. Yokoyama, Hampton L. Leonard
منشور في 2024Revisão -
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Genetic risk factor clustering within and across neurodegenerative diseases حسب Mathew J. Koretsky, Chelsea X. Alvarado, Mary B. Makarious, Dan Vitale, Kristin Levine, Sara Bandrés‐Ciga, Anant Dadu, Sonja W. Scholz, Lana Sargent, Faraz Faghri, Hirotaka Iwaki, Cornelis Blauwendraat, Andrew Singleton, Mike A. Nalls, Hampton L. Leonard
منشور في 2023Artigo -
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Sleep disturbances as risk factors for neurodegeneration later in life حسب Emily Simmonds, Kristin Levine, Jun Han, Hirotaka Iwaki, Mathew J. Koretsky, Nicole Kuznetsov, Faraz Faghri, Caroline Warly Solsberg, Artur Francisco Schumacher Schuh, Lietsel Jones, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Andrew Singleton, Valentina Escott‐Price, Hampton L. Leonard, Mike A. Nalls
منشور في 2023Pré-impressão -
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GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and Analysis حسب Dan Vitale, Mathew J. Koretsky, Nicole Kuznetsov, Samantha Hong, Jessica Martin, M R James, Mary B. Makarious, Hampton L. Leonard, Hirotaka Iwaki, Faraz Faghri, Cornelis Blauwendraat, Andrew Singleton, Yeajin Song, Kristin Levine, Ashwin Ashok Kumar Sreelatha, Zih‐Hua Fang, Mike A. Nalls
منشور في 2024Pré-impressão -
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GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and Analysis حسب Dan Vitale, Mathew J. Koretsky, Nicole Kuznetsov, Samantha Hong, Jessica Martin, M R James, Mary B. Makarious, Hampton L. Leonard, Hirotaka Iwaki, Faraz Faghri, Cornelis Blauwendraat, Andrew B. Singleton, Yeajin Song, Kristin Levine, Ashwin Ashok Kumar Sreelatha, Zih‐Hua Fang, Mike A. Nalls
منشور في 2024Artigo -
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Multi-ancestry meta-analysis and fine-mapping in Alzheimer’s disease حسب Julie Lake, Caroline Warly Solsberg, Jonggeol Jeffrey Kim, Juliana Acosta‐Uribe, Mary B. Makarious, Zizheng Li, Kristin Levine, Peter Heutink, Chelsea X. Alvarado, Dan Vitale, Sarang Kang, Jungsoo Gim, Kun Ho Lee, Stefanie Danielle Piña‐Escudero, Luigi Ferrucci, Andrew Singleton, Cornelis Blauwendraat, Mike A. Nalls, Jennifer S. Yokoyama, Hampton L. Leonard
منشور في 2023Revisão -
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The Neurodegenerative Disease Knowledge Portal حسب Allison A. Dilliott, Maria C. Costanzo, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Bradford Casey, Quy Hoang, Hirotaka Iwaki, Dongkeun Jang, Jonggeol Jeffrey Kim, Hampton L. Leonard, Kristin Levine, Mary B. Makarious, Trang Thi Huyen Nguyen, Guy A. Rouleau, Andrew Singleton, Patrick Smadbeck, Justin Solle, Dan Vitale, Mike A. Nalls, Jason Flannick, Noël P. Burtt, Sali M.K. Farhan
منشور في 2025Revisão -
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Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores حسب Paula Saffie Awad, Spencer Grant, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea, Artur Francisco Schumacher Schuh, Kristin Levine, Dan Vitale, Mathew J. Koretsky, Jeffrey Kim, Thiago Peixoto Leal, María Teresa Periñán, Sumit Dey, Alastair Noyce, Armando Reyes‐Palomares, Noela Rodríguez-Losada, Jia Nee Foo, Wael Mohamed, Karl Heilbron, Lucy Norcliffe‐Kaufmann, Mie Rizig, Njideka Okubadejo, Mike A. Nalls, Cornelis Blauwendraat, Andrew B. Singleton, Hampton L. Leonard, Ignácio F. Mata, Sara Bandrés‐Ciga
منشور في 2025Artigo -
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NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations حسب Sara Bandrés‐Ciga, Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine, Hampton L. Leonard, Mary B. Makarious, Hirotaka Iwaki, Peter Wild Crea, Dena Hernández, Sampath Arepalli, Kimberley J. Billingsley, Katja Lohmann, Christine Klein, Steven Lubbe, Edwin Jabbari, Paula Saffie Awad, Derek P. Narendra, Armando Reyes‐Palomares, John P. Quinn, Claudia Schulte, Huw R. Morris, Bryan J. Traynor, Sonja W. Scholz, Henry Houlden, John Hardy, Sonya B. Dumanis, Ekemini Riley, Cornelis Blauwendraat, Andrew Singleton, Mike A. Nalls, Janina M. Jeff, Dan Vitale
منشور في 2023Pré-impressão -
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<scp>NeuroBooster</scp> Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations حسب Sara Bandrés‐Ciga, Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine, Hampton L. Leonard, Mary B. Makarious, Hirotaka Iwaki, Peter Wild Crea, Dena Hernández, Sampath Arepalli, Kimberley J. Billingsley, Katja Lohmann, Christine Klein, Steven Lubbe, Edwin Jabbari, Paula Saffie Awad, Derek P. Narendra, Armando Reyes‐Palomares, John P. Quinn, Claudia Schulte, Huw R. Morris, Bryan J. Traynor, Sonja W. Scholz, Henry Houlden, John Hardy, Sonya B. Dumanis, Ekemini Riley, Cornelis Blauwendraat, Andrew Singleton, Mike A. Nalls, Janina M. Jeff, Dan Vitale
منشور في 2024Artigo -
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Genome‐Wide Analysis of Structural Variants in Parkinson Disease حسب Kimberley J. Billingsley, Jinhui Ding, Pilar Álvarez Jerez, Anastasia Illarionova, Kristin Levine, Francis P. Grenn, Mary B. Makarious, Anni Moore, Dan Vitale, Xylena Reed, Dena Hernández, Ali Torkamani, Mina Ryten, John Hardy, Ruth Chia, Sonja W. Scholz, Bryan J. Traynor, Clifton L. Dalgard, Debra Ehrlich, Toshiko Tanaka, Luigi Ferrucci, Thomas G. Beach, Geidy E. Serrano, John P. Quinn, Vivien J. Bubb, Ryan L. Collins, Xuefang Zhao, Mark Walker, Emma Pierce‐Hoffman, Harrison Brand, Michael E. Talkowski, Bradford Casey, Mark Cookson, Androo J. Markham, Mike A. Nalls, Medhat Mahmoud, Fritz J. Sedlazeck, Cornelis Blauwendraat, J. Raphael Gibbs, Andrew Singleton
منشور في 2023Artigo -
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Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study حسب Mie Rizig, Sara Bandrés‐Ciga, Mary B. Makarious, Oluwadamilola O. Ojo, Peter Wild Crea, Oladunni Abiodun, Kristin Levine, Sani Abubakar, Charles Achoru, Dan Vitale, Olaleye Adeniji, Osigwe P. Agabi, Mathew J. Koretsky, Uchechi Agulanna, Deborah J. Hall, Rufus Akinyemi, Tao Xie, Mohammed Ali, Ejaz A. Shamim, Ifeyinwa Ani‐Osheku, Mahesh Padmanaban, Ohwotemu Arigbodi, David G. Standaert, Abiodun Bello, Marissa Dean, Cyril Erameh, Inas Elsayed, Temitope Farombi, Olaitan Okunoye, Bimbo Fawale, Kimberley J. Billingsley, Frank Imarhiagbe, Pilar Álvarez Jerez, Emmanuel Iwuozo, Breeana Baker, Morenikeji Komolafe, Laksh Malik, Paul Osemeke Nwani, Kensuke Daida, Ernest Nwazor, Abigail Miano‐Burkhardt, Yakub Nyandaiti, Zih‐Hua Fang, Yahaya Obiabo, Jillian H. Kluss, Olanike Odeniyi, Dena Hernández, Francis Odiase, Nahid Tayebi, FI Ojini, Ellen Sidranksy, Gerald Onwuegbuzie, Andrea D'Souza, Godwin Osaigbovo, Bahafta Berhe, Nosakhare Osemwegie, Xylena Reed, Olajumoke Oshinaike, Hampton L. Leonard, Folajimi Otubogun, Chelsea X. Alvarado, Shyngle Oyakhire, Simon Ozomma, Sarah Samuel, Funmilola Tolulope Taiwo, Kolawole Wahab, Yusuf Zubair, Hirotaka Iwaki, Jonggeol Jeffrey Kim, Huw R. Morris, John Hardy, Mike A. Nalls, Karl Heilbron, Lucy Norcliffe‐Kaufmann, Cornelis Blauwendraat, Henry Houlden, Andrew Singleton, Njideka Okubadejo, Njideka Okubadejo, Oluwadamilola O. Ojo, Oladunni Abiodun, Charles Achoru, Osigwe P. Agabi, Uchechi Agulanna, Rufus Akinyemi, Mohammed Ali, Ifeyinwa Ani‐Osheku, Ohwotemu Arigbodi, Abiodun Bello, Cyril Erameh, Temitope Farombi, Bimbo Fawale, Frank Imarhiagbe, Emmanuel Iwuozo, Morenikeji Komolafe, Paul Osemeke Nwani, Ernest Nwazor, Yakub Nyandaiti, Yahaya Obiabo, Olanike Odeniyi
منشور في 2023Revisão -
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Large-scale genetic characterization of Parkinson′s disease in the African and African admixed populations حسب Fulya Akçimen, Kimberly Paquette, Peter Wild Crea, Paula Saffie Awad, Charles Achoru, Funmilola Taiwo, Simon Ozomma, Gerald Onwuegbuzie, Marzieh Khani, Spencer Grant, Lukman Owolabi, Chiamaka Okereke, Olajumoke Oshinaike, Emmanuel Iwuozo, Paul Suhwan Lee, Shyngle Oyakhire, Nosakhare Osemwegie, Kensuke Daida, Sani Abubakar, Adedunni Olusanya, Mariam Isayan, Rami Traurig, Adebimpe Ogunmodede, Sarah Samuel, Mary B. Makarious, Fawzy A. Saad, Rashidat Amoke Olanigan, Kristin Levine, Ewere Marie Ogbimi, Dan Vitale, Francis Odiase, Mathew J. Koretsky, FI Ojini, Olanike Odeniyi, Zih‐Hua Fang, Nkechi Obianozie, Deborah J. Hall, Ernest Nwazor, Tao Xie, Francisca Nwaokorie, Mahesh Padmanaban, Paul Osemeke Nwani, Ejaz A. Shamim, Alero Nnama, David G. Standaert, Morenikeji Komolafe, Marissa Dean, Godwin Osaigbovo, Elizabeth A. Disbrow, Ismail O. Ishola, Ashley Rawls, Frank Imarhiagbe, Shivika Chandra, Cyril Erameh, Vanessa K. Hinson, Naomi Louie, Ahmed O. Idowu, Justin Solle, Scott A. Norris, Abdullahi Adinoyi Ibrahim, Camilla Kilbane, Gauthaman Sukumar, Lisa Shulman, Daniel Ezuduemoih, Julia Staisch, Sarah Breaux, Clifton L. Dalgard, Erin R. Foster, Abiodun Bello, Andrew Ameri, Raquel Real, Erica Ikwenu, Huw R. Morris, Roosevelt Anyanwu, Erin Furr‐Stimming, Kimberley J. Billingsley, Wemimo Alaofin, Pilar Álvarez Jerez, Osigwe P. Agabi, Dena Hernández, Rufus Akinyemi, Sampath Arepalli, Laksh Malik, Raymond Owolabi, Yakub Nyandaiti, Hampton L. Leonard, Kolawole Wahab, Kathryn Step, Oladunni Abiodun, Carlos Hernández, Fatimah Binta Abdullahi, Hirotaka Iwaki, Soraya Bardien, Christine Klein, John Hardy, Henry Houlden, Kamalini Ghosh Galvelis, Mike A. Nalls, Nabila Dahodwala, Whitley W. Aamodt
منشور في 2025Pré-impressão -
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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) حسب Clodagh Towns, Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar, Alejandro Martínez-Carrasco, Mary B. Makarious, Bradford Casey, Dan Vitale, Kristin Levine, Hampton L. Leonard, Caroline B. Pantazis, Laurel A. Screven, Dena Hernández, Claire Wegel, Justin Solle, Mike A. Nalls, Cornelis Blauwendraat, Andrew Singleton, Manuela Tan, Hirotaka Iwaki, Huw R. Morris, Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, M. Leonor Bustamante, Patricio Olguı́n, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo, Gonzálo Arboleda, Jorge Orozco, Marlene Jiménez-Del-Río, Álvaro Hernández-Flores, Mohamed Salama, Walaa A. Kamel, Yared Z. Zewde, Alexis Brice, Jean‐Christophe Corvol, Ana Westenberger, Anastasia Illarionova, Brit Mollenhauer, Christine Klein, Eva‐Juliane Vollstedt, Franziska Hopfner, Günter U. Höglinger, Harutyun Madoev, Joanne Trinh, Johanna Junker, Katja Lohmann, Lara M. Lange, Manu Sharma, Sergiu Groppa, Thomas Gasser, Zih‐Hua Fang, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Ioannis E. Dagklis, Ioannis Tarnanas, Leonidas Stefanis, María Stamelou, Efthymios Dadiotis, Alex Medina, Germaine Hiu-Fai Chan, Nancy Y. Ip, Nelson Yuk-Fai Cheung, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya KP, Pramod Kumar Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Enza Maria Valente
منشور في 2023Artigo -
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The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population حسب Lara M. Lange, Kristin Levine, Susan H. Fox, Connie Marras, Nazish Rafique, Nicole Kuznetsov, Dan Vitale, Hirotaka Iwaki, Katja Lohmann, Luca Marsili, Alberto J. Espay, Peter Bauer, Christian Beetz, Jessica Martin, Stewart A. Factor, Lenora A. Higginbotham, Honglei Chen, Hampton L. Leonard, Mike A. Nalls, Niccolò E. Mencacci, Huw R. Morris, Andrew Singleton, Christine Klein, Cornelis Blauwendraat, Zih‐Hua Fang, Emilia Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Kõks, Alexander Zimprich, Artur Francisco Schumacher Schuh, Carlos Roberto de Mello Rieder, Paula Saffie Awad, Vítor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Patricio Olguı́n, Marcelo Miranda, M. Leonor Bustamante, Pedro Chaná, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, Wei Luo, Gonzálo Arboleda, Jorge Orozco, Marlene Jiménez-Del-Río, Álvaro Hernández-Flores, Mohamed Salama, Walaa A. Kamel, Yared Z. Zewde, Alexis Brice, Jean‐Christophe Corvol, Ana Westenberger, Eva‐Juliane Vollstedt, Harutyun Madoev, Joanne Trinh, Johanna Junker, Anastasia Illarionova, Brit Mollenhauer, Franziska Hopfner, Günter U. Höglinger, Manu Sharma, Thomas Gasser, Sergiu Groppa, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Efthymios Dadiotis, Ioannis E. Dagklis, Ioannis Tarnanas, Leonidas Stefanis, María Stamelou, Alex Medina, Germaine Hiu-Fai Chan, Nelson Yuk-Fai Cheung, Nancy Y. Ip, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya KP, Pramod Kr. Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Monica Gagliardi, Enza Maria Valente, Micol Avenali
منشور في 2025Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Medicine
Disease
Gene
Genetics
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Computational biology
Computer science
Internal medicine
Pathology
Population
Environmental health
Genetic association
Genotyping
Neurodegeneration
Neuroscience
Biobank
Bioinformatics
Genome
Gerontology
Parkinson's disease
Psychology
Amyotrophic lateral sclerosis
Biochemistry
Context (archaeology)
Dementia
Genetic diversity
Haplotype