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A cellular taxonomy of the adult human spinal cord
A cellular taxonomy of the adult human spinal cord
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A cellular taxonomy of the adult human spinal cord

Yadav, Archana ; Matson, Kaya J.E. ; Li, Li ; Hua, Isabelle ; Petrescu, Joana ; Kang, Kristy ; Alkaslasi, Mor R. ; Lee, Dylan I. ; Hasan, Saadia ; Galuta, Ahmad ; Dedek, Annemarie ; Ameri, Sara ; Parnell, Jessica ; Alshardan, Mohammad M. ; Qumqumji, Feras Abbas ; Alhamad, Saud M. ; Wang, Alick Pingbei ; Poulen, Gaetan ; Lonjon, Nicolas ; Vachiery-Lahaye, Florence ; Gaur, Pallavi ; Nalls, Mike A. ; Qi, Yue A. ; Maric, Dragan ; Ward, Michael E. ; Hildebrand, Michael E. ; Mery, Pierre-Francois ; Bourinet, Emmanuel ; Bauchet, Luc ; Tsai, Eve C. ; Phatnani, Hemali ; Le Pichon, Claire E. ; Menon, Vilas ; Levine, Ariel J.

Neuron (Cambridge, Mass.), 2023-02, Vol.111 (3), p.328-344.e7 [Periódico revisado por pares]

United States: Elsevier Inc

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2
ABCA7 p.G215S as potential protective factor for Alzheimer’s disease
ABCA7 p.G215S as potential protective factor for Alzheimer’s disease
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ABCA7 p.G215S as potential protective factor for Alzheimer’s disease

Sassi, C ; Nalls, M.A ; Ridge, P.G ; Gibbs, R ; Ding, J ; Lupton, M.K ; Troakes, C ; Lunnon, K ; Al-Sarraj, S ; Brown, K.S ; Medway, C ; Clement, N ; Lord, J ; Turton, J ; Bras, J ; Almeida, M.R ; Holstege, H ; Louwersheimer, E ; van der Flier, W ; Scheltens, P ; Van Swieten, J.C ; Santana, I ; Oliveira, C ; Morgan, K ; Powell, J.F ; Kauwe, J.S ; Cruchaga, C ; Goate, A.M ; Singleton, A.B ; Guerreiro, R ; Hardy, J

Neurobiology of aging, 2016-10, Vol.46, p.235.e1-235.e9 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X
Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X
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Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X

Cheng, Ching-Yu ; Kao, W H Linda ; Patterson, Nick ; Tandon, Arti ; Haiman, Christopher A ; Harris, Tamara B ; Xing, Chao ; John, Esther M ; Ambrosone, Christine B ; Brancati, Frederick L ; Coresh, Josef ; Press, Michael F ; Parekh, Rulan S ; Klag, Michael J ; Meoni, Lucy A ; Hsueh, Wen-Chi ; Fejerman, Laura ; Pawlikowska, Ludmila ; Freedman, Matthew L ; Jandorf, Lina H ; Bandera, Elisa V ; Ciupak, Gregory L ; Nalls, Michael A ; Akylbekova, Ermeg L ; Orwoll, Eric S ; Leak, Tennille S ; Miljkovic, Iva ; Li, Rongling ; Ursin, Giske ; Bernstein, Leslie ; Ardlie, Kristin ; Taylor, Herman A ; Boerwinckle, Eric ; Zmuda, Joseph M ; Henderson, Brian E ; Wilson, James G ; Reich, David McCarthy, Mark I.

PLoS genetics, 2009-05, Vol.5 (5), p.e1000490-e1000490 [Periódico revisado por pares]

United States: Public Library of Science

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4
Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies
Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies
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Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies

Nalls, Michael A. ; Wilson, James G. ; Patterson, Nick J. ; Tandon, Arti ; Zmuda, Joseph M. ; Huntsman, Scott ; Garcia, Melissa ; Hu, Donglei ; Li, Rongling ; Beamer, Brock A. ; Patel, Kushang V. ; Akylbekova, Ermeg L. ; Files, Joe C. ; Hardy, Cheryl L. ; Buxbaum, Sarah G. ; Taylor, Herman A. ; Reich, David ; Harris, Tamara B. ; Ziv, Elad

American journal of human genetics, 2008-01, Vol.82 (1), p.81-87 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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5
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
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Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

Moskvina, Valentina ; Harold, Denise ; Russo, GianCarlo ; Vedernikov, Alexey ; Sharma, Manu ; Saad, Mohamad ; Holmans, Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J. Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Owen, Michael J ; O’Donovan, Michael C ; Williams, Julie ; Morris, Huw R ; Williams, Nigel M

JAMA neurology, 2013-10, Vol.70 (10), p.1268-1276 [Periódico revisado por pares]

United States: American Medical Association

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6
Are Myocardial Infarction-Associated Single-Nucleotide Polymorphisms Associated With Ischemic Stroke?
Are Myocardial Infarction-Associated Single-Nucleotide Polymorphisms Associated With Ischemic Stroke?
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Are Myocardial Infarction-Associated Single-Nucleotide Polymorphisms Associated With Ischemic Stroke?

CHENG, Yu-Ching ; ANDERSON, Christopher D ; BARLERA, Simona ; BIFFI, Alessandro ; BOOKMAN, Ebony ; BROTT, Thomas G ; BROWN, Robert D ; FANG CHEN ; CHEN, Wei-Min ; CIUSANI, Emilio ; COLE, John W ; CORTELLINI, Lynelle ; BIONE, Silvia ; DANESH, John ; DOHENY, Kimberly ; FERRUCCI, Luigi ; GRAZIA FRANZOSI, Maria ; FROSSARD, Philippe ; FURIE, Karen L ; GOLLEDGE, Jonathan ; HANKEY, Graeme J ; HERNANDEZ, Dena ; HOLLIDAY, Elizabeth G ; KEENE, Keith ; HSU, Fang-Chi ; JANNES, Jim ; KAMAL, Ayeesha ; SALEEM KHAN, Muhammad ; KITTNER, Steven J ; KOBLAR, Simon A ; LEWIS, Martin ; LINCZ, Lisa ; LISA, Antonella ; MATARIN, Mar ; MAGUIRE, Jane M ; MOSCATO, Pablo ; MYCHALECKYJ, Josyf C ; PARATI, Eugenio A ; PAROLO, Silvia ; PUGH, Elizabeth ; ROST, Natalia S ; SCHALLERT, Michael ; SCHMIDT, Helena ; SCOTT, Rodney J ; STURM, Jonathan W ; NALLS, Michael ; YADAV, Sunaina ; ZAIDI, Moazzam ; BONCORAGLIO, Giorgio B ; ROYCE LEVI, Christopher ; MESCHIA, James F ; ROSAND, Jonathan ; SALE, Michele ; SALEHEEN, Danish ; SCHMIDT, Reinhold ; RASHEED, Asif ; ZEGINIGG, Marion ; ATTIA, John ; BAKER, Ross

Stroke (1970), 2012-04, Vol.43 (4), p.980-986 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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7
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

FOX, Ervin R ; HUNTER YOUNG, J ; RAMACHANDRAN, VasanS ; POLAK, JosefF ; FABSITZ, Richard R ; DRIES, Daniel L ; FARLOW, Deborah N ; REDLINE, Susan ; ADEYEMO, Adebowale ; HIRSCHORN, Joel N ; SUN, Yan V ; WYATT, Sharon B ; YALI LI ; PENMAN, Alan D ; PALMAS, Walter ; ROTTER, Jerome I ; TOWNSEND, Raymond R ; DOUMATEY, Ayo P ; TAYO, Bamidele O ; MOSLEY, Thomas H ; LYON, Helen N ; KANG, Sun J ; ROTIMI, Charles N ; DREISBACH, Albert W ; COOPER, Richard S ; FRANCESCHINI, Nora ; CURB, J. David ; MARTIN, Lisa W ; EATON, Charles B ; KARDIA, Sharon L. R ; TAYLOR, Herman A ; CAULFIELD, Mark J ; EHRET, Georg B ; JOHNSON, Toby ; KEATING, Brendan J ; CHAKRAVARTI, Aravinda ; XIAOFENG ZHU ; LEVY, Daniel ; MUSANI, Solomon K ; KIANG LIU ; MORRISON, Alanna C ; GANESH, Santhi ; KUTLAR, Abdullah

Human molecular genetics, 2011-06, Vol.20 (11), p.2273-2284 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Laaksovirta, Hannu, MD ; Peuralinna, Terhi, MSc ; Schymick, Jennifer C, PhD ; Scholz, Sonja W, MD ; Lai, Shaoi-Lin, MD ; Myllykangas, Liisa, MD ; Sulkava, Raimo, MD ; Jansson, Lilja ; Hernandez, Dena G, MSc ; Gibbs, J Raphael, BS ; Nalls, Michael A, PhD ; Heckerman, David, MD ; Tienari, Pentti J, MD ; Traynor, Bryan J, Dr

Lancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]

England: Elsevier Ltd

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9
Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage
Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage
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Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage

ANDERSON, Christopher D ; BIFFI, Alessandro ; VISWANATHAN, Anand ; WORRALL, Bradford B ; BROTT, Thomas G ; GOLDSTEIN, Joshua N ; BROWN, Devin ; BRODERICK, Joseph P ; NORRVING, Bo ; GREENBERG, Steven M ; SILLIMAN, Scott L ; HANSEN, Björn M ; NALLS, Michael A ; TIRSCHWELL, David L ; LINDGREN, Arne ; SLOWIK, Agnieszka ; SCHMIDT, Reinhold ; SELIM, Magdy ; ROQUER, Jaume ; MONTANER, Joan ; SINGLETON, Andrew B ; KIDWELL, Chelsea S ; WOO, Daniel ; DEVAN, William J ; FURIE, Karen L ; MESCHIA, James F ; ROSAND, Jonathan ; SCHWAB, Kristin ; AYRES, Alison M ; VALANT, Valerie ; ROSS, Owen A ; ROST, Natalia S ; SAXENA, Richa

Stroke (1970), 2013-03, Vol.44 (3), p.612-619 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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10
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection
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Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

Debette, Stéphanie ; Kamatani, Yoichiro ; Metso, Tiina M ; Kloss, Manja ; Chauhan, Ganesh ; Engelter, Stefan T ; Pezzini, Alessandro ; Thijs, Vincent ; Markus, Hugh S ; Dichgans, Martin ; Wolf, Christiane ; Dittrich, Ralf ; Touzé, Emmanuel ; Southerland, Andrew M ; Samson, Yves ; Abboud, Shérine ; Béjot, Yannick ; Caso, Valeria ; Bersano, Anna ; Gschwendtner, Andreas ; Sessa, Maria ; Cole, John ; Lamy, Chantal ; Medeiros, Elisabeth ; Beretta, Simone ; Bonati, Leo H ; Grau, Armin J ; Michel, Patrik ; Majersik, Jennifer J ; Sharma, Pankaj ; Kalashnikova, Ludmila ; Nazarova, Maria ; Dobrynina, Larisa ; Bartels, Eva ; Guillon, Benoit ; van den Herik, Evita G ; Fernandez-Cadenas, Israel ; Jood, Katarina ; Nalls, Michael A ; De Leeuw, Frank-Erik ; Jern, Christina ; Cheng, Yu-Ching ; Werner, Inge ; Metso, Antti J ; Lichy, Christoph ; Lyrer, Philippe A ; Brandt, Tobias ; Boncoraglio, Giorgio B ; Wichmann, Heinz-Erich ; Gieger, Christian ; Johnson, Andrew D ; Böttcher, Thomas ; Castellano, Maurizio ; Arveiler, Dominique ; Ikram, M Arfan ; Breteler, Monique M B ; Padovani, Alessandro ; Meschia, James F ; Kuhlenbäumer, Gregor ; Rolfs, Arndt ; Worrall, Bradford B ; Ringelstein, Erich-Bernd ; Zelenika, Diana ; Tatlisumak, Turgut ; Lathrop, Mark ; Leys, Didier ; Amouyel, Philippe ; Dallongeville, Jean

Nature genetics, 2015-01, Vol.47 (1), p.78-83 [Periódico revisado por pares]

United States: Nature Publishing Group

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