Mike A Nalls: search on Z-Library

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1

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli, Bras, Jose, Young, Emily, von

Journal:

The Lancet Neurology

Year:

2019

Language:

english

File:

PDF, 2.94 MB

english, 2019

2

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Jansen, Iris E., Ye, Hui, Heetveld, Sasja, Lechler, Marie C., Michels, Helen, Seinstra, Renée I., Lubbe, Steven J., Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J. Raphael, Nalls, Mike A.

Journal:

Year:

2017

Language:

english

File:

PDF, 7.89 MB

english, 2017

3

A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci

Chang, Diana, Nalls, Mike A, Hallgrímsdóttir, Ingileif B, Hunkapiller, Julie, van der Brug, Marcel, Cai, Fang, Kerchner, Geoffrey A, Ayalon, Gai, Bingol, Baris, Sheng, Morgan, Hinds, David, Behrens, T

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 947 KB

english, 2017

4

Genome-wide estimates of heritability and genetic correlations in essential tremor

Diez-Fairen, Monica, Bandres-Ciga, Sara, Houle, Gabrielle, Nalls, Mike A., Girard, Simon L., Dion, Patrick A., Blauwendraat, Cornelis, Singleton, Andrew B., Rouleau, Guy A., Pastor, Pau

Journal:

Parkinsonism & Related Disorders

Year:

2019

Language:

english

File:

PDF, 472 KB

english, 2019

5

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Ar

Journal:

Nature Genetics

Year:

2014

Language:

english

File:

PDF, 535 KB

english, 2014

6

Genetic diversity is a predictor of mortality in humans

Bihlmeyer, Nathan A, Brody, Jennifer A, Smith, Albert, Lunetta, Kathryn L, Nalls, Mike, Smith, Jennifer A, Tanaka, Toshiko, Davies, Gail, Yu, Lei, Mirza, Saira, Teumer, Alexander, Coresh, Josef, Panko

Journal:

Year:

2014

Language:

english

File:

PDF, 1.11 MB

english, 2014

7

ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies

Blauwendraat, Cornelis, Nalls, Mike A., Federoff, Monica, Pletnikova, Olga, Ding, Jinhui, Letson, Christopher, Geiger, Joshua T., Gibbs, J. Raphael, Hernandez, Dena G., Troncoso, Juan C., Simón-Sánche

Journal:

Movement Disorders

Year:

2017

Language:

english

File:

PDF, 235 KB

english, 2017

8

Anticholinergic Drug Induced Cognitive and Physical Impairment: Results from the InCHIANTI Study

Sargent, Lana, Nalls, Mike, Amella, Elaine J, Mueller, Martina, Lageman, Sarah K, Bandinelli, Stefania, Colpo, Marco, Slattum, Patricia W, Singleton, Andrew, Ferrucci, Luigi

Journal:

The Journals of Gerontology Series A Biological Sciences and Medical Sciences

Year:

2018

Language:

english

File:

PDF, 641 KB

english, 2018

9

Genetic risk and age in Parkinson's disease: Continuum not stratum

Nalls, Mike A., Escott-Price, Valentina, Williams, Nigel M., Lubbe, Steven, Keller, Margaux F., Morris, Huw R., Singleton, Andrew B.

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 288 KB

english, 2015

10

The genetic architecture of Parkinson's disease

Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

Journal:

The Lancet Neurology

Year:

2019

File:

PDF, 244 KB

2019

11

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke

Auer, Paul L., Nalls, Mike, Meschia, James F., Worrall, Bradford B., Longstreth, W. T., Seshadri, Sudha, Kooperberg, Charles, Burger, Kathleen M., Carlson, Christopher S., Carty, Cara L., Chen, Wei-Mi

Journal:

Year:

2015

Language:

english

File:

PDF, 233 KB

english, 2015

12

Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans

Carty, Cara L., Keene, Keith L., Cheng, Yu-Ching, Meschia, James F., Chen, Wei-Min, Nalls, Mike, Bis, Joshua C., Kittner, Steven J., Rich, Stephen S., Tajuddin, Salman, Zonderman, Alan B., Evans, Mich

Journal:

Year:

2015

Language:

english

File:

PDF, 1.19 MB

english, 2015

13

Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis

Siitonen, Ari, Kytövuori, Laura, Nalls, Mike A., Gibbs, Raphael, Hernandez, Dena G., Ylikotila, Pauli, Peltonen, Markku, Singleton, Andrew B., Majamaa, Kari

Journal:

Scientific Reports

Year:

2019

File:

PDF, 1.16 MB

2019

14

Is the MC1R variant p.R160W associated with Parkinson's?

Lubbe, Steven J., Escott-Price, Valentina, Brice, Alexis, Gasser, Thomas, Hardy, John, Heutink, Peter, Sharma, Manu, Wood, Nicholas W., Nalls, Mike, Singleton, Andrew B., Williams, Nigel M., Morris, H

Journal:

Annals of Neurology

Year:

2016

Language:

english

File:

PDF, 74 KB

english, 2016

15

Mendelian Randomization - the Key to Understanding Aspects of Parkinson's Disease Causation?

Noyce, Alastair J., Nalls, Mike A.

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 484 KB

english, 2015

16

Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study

Tin, Adrienne, Köttgen, Anna, Folsom, Aaron R, Maruthur, Nisa M, Tajuddin, Salman M, Nalls, Mike A, Evans, Michele K, Zonderman, Alan B, Friedrich, Christopher A, Boerwinkle, Eric, Coresh, Josef, Kao,

Journal:

Year:

2015

Language:

english

File:

PDF, 721 KB

english, 2015

17

ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion

Chiò, Adriano, Mora, Gabriele, Sabatelli, Mario, Caponnetto, Claudia, Lunetta, Christian, Traynor, Bryan J., Johnson, Janel O., Nalls, Mike A., Calvo, Andrea, Moglia, Cristina, Borghero, Giuseppe, Tro

Journal:

Neurobiology of Aging

Year:

2015

File:

PDF, 259 KB

2015

18

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

Nicolas, Aude, Kenna, Kevin P., Renton, Alan E., Ticozzi, Nicola, Faghri, Faraz, Chia, Ruth, Dominov, Janice A., Kenna, Brendan J., Nalls, Mike A., Keagle, Pamela, Rivera, Alberto M., van Rheenen, Wou

Journal:

Year:

2018

Language:

english

File:

PDF, 2.25 MB

english, 2018

19

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans

Foo, Jia Nee, Chew, Elaine Guo Yan, Chung, Sun Ju, Peng, Rong, Blauwendraat, Cornelis, Nalls, Mike A., Mok, Kin Y., Satake, Wataru, Toda, Tatsushi, Chao, Yinxia, Tan, Louis C. S., Tandiono, Moses, Lia

Journal:

Year:

2020

File:

PDF, 1.23 MB

2020

20

Comprehensive assessment of PINK1 variants in Parkinson's disease

Krohn, Lynne, Grenn, Francis P., Makarious, Mary B., Kim, Jonggeol Jeffrey, Bandres-Ciga, Sara, Roosen, Dorien A., Gan-Or, Ziv, Nalls, Mike A., Singleton, Andrew B., Blauwendraat, Cornelis

Journal:

Neurobiology of Aging

Year:

2020

File:

PDF, 383 KB

2020

21

Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)

Nalls, Mike A., Keller, Margaux F., Hernandez, Dena G., Chen, Lan, Stone, David J., Singleton, Andrew B.

Journal:

Movement Disorders

Year:

2016

Language:

english

File:

PDF, 638 KB

english, 2016

22

Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort study

Tajuddin, Salman M., Nalls, Mike A., Zonderman, Alan B., Evans, Michele K.

Journal:

Journal of Translational Medicine

Year:

2017

Language:

english

File:

PDF, 845 KB

english, 2017

23

Shared mechanisms for cognitive impairment and physical frailty: A model for complex systems

Sargent, Lana, Nalls, Mike, Amella, Elaine J., Slattum, Patricia W., Mueller, Martina, Bandinelli, Stefania, Tian, Qu, SwiftâScanlan, Theresa, Lageman, Sarah K., Singleton, Andrew

Journal:

Alzheimer s & Dementia Translational Research & Clinical Interventions

Year:

2020

File:

PDF, 1.97 MB

2020

24

Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinsonâs disease

Brown, Emmeline E., Blauwendraat, Cornelis, Trinh, Joanne, Rizig, Mie, Nalls, Mike A., Leveille, Etienne, Ruskey, Jennifer A., Jonvik, Hallgeir, Tan, Manuela M.X., Bandres-Ciga, Sara, Hassin-Baer, Sha

Journal:

Neurobiology of Aging

Year:

2020

File:

PDF, 1.28 MB

2020

25

Plasma Levels of Soluble IL-2 Receptor α

Durda, Peter, Sabourin, Jeremy, Lange, Ethan M., Nalls, Mike A., Mychaleckyj, Josyf C., Jenny, Nancy Swords, Li, Jin, Walston, Jeremy, Harris, Tamara B., Psaty, Bruce M., Valdar, William, Liu, Yongmei

Journal:

Arteriosclerosis Thrombosis and Vascular Biology

Year:

2015

Language:

english

File:

PDF, 584 KB

english, 2015

26

Dystonia; a roadmap is needed for future genetic studies

Gan-Or, Ziv, Mencacci, Niccolò E., Nalls, Mike A.

Journal:

Parkinsonism & Related Disorders

Year:

2018

Language:

english

File:

PDF, 179 KB

english, 2018

27

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

Nalls, Mike A., Bras, Jose, Hernandez, Dena G., Keller, Margaux F., Majounie, Elisa, Renton, Alan E., Saad, Mohamad, Jansen, Iris, Guerreiro, Rita, Lubbe, Steven, Plagnol, Vincent, Gibbs, J. Raphael,

Journal:

Neurobiology of Aging

Year:

2015

Language:

english

File:

PDF, 740 KB

english, 2015

28

The genetic architecture of Parkinson's disease

Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

Journal:

The Lancet Neurology

Year:

2019

Language:

english

File:

PDF, 244 KB

english, 2019

29

A 6.4 Mb Duplication of the α-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism

Kara, Eleanna, Kiely, Aoife P., Proukakis, Christos, Giffin, Nicola, Love, Seth, Hehir, Jason, Rantell, Khadija, Pandraud, Amelie, Hernandez, Dena G., Nacheva, Elizabeth, Pittman, Alan M., Nalls, Mike

Journal:

Year:

2014

Language:

english

File:

PDF, 458 KB

english, 2014

30

A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach

Traylor, Matthew, Mäkelä, Kari-Matti, Kilarski, Laura L., Holliday, Elizabeth G., Devan, William J., Nalls, Mike A., Wiggins, Kerri L., Zhao, Wei, Cheng, Yu-Ching, Achterberg, Sefanja, Malik, Rainer,

Journal:

Year:

2014

Language:

english

File:

PDF, 996 KB

english, 2014

31

Polygenic risk of Parkinson disease is correlated with disease age at onset

Escott-Price, Valentina, Nalls, Mike A., Morris, Huw R., Lubbe, Steven, Brice, Alexis, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Hardy, John, Singleton, Andrew B., Williams, Nigel M.

Journal:

Annals of Neurology

Year:

2015

Language:

english

File:

PDF, 215 KB

english, 2015

32

A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease

Kristiansen, Madeleine, Maple-Grødem, Jodi, Alves, Guido, Arepalli, Sampath, Hernandez, Dena G., Iwaki, Hirotaka, Nalls, Mike A., Singleton, Andrew, Tysnes, Ole-Bjørn, Toft, Mathias, Pihlstrøm, Lasse

Journal:

Movement Disorders

Year:

2018

Language:

english

File:

PDF, 121 KB

english, 2018

33

Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease

Leonard, Hampton, Blauwendraat, Cornelis, Krohn, Lynne, Faghri, Faraz, Iwaki, Hirotaka, Ferguson, Glen, Day-Williams, Aaron G, Stone, David J, Singleton, Andrew B, Nalls, Mike A, Gan-Or, Ziv

Journal:

Journal of Medical Genetics

Year:

2019

File:

PDF, 613 KB

2019

34

Parkinsonâs disease determinants, prediction and geneâenvironment interactions in the UK Biobank

Jacobs, Benjamin Meir, Belete, Daniel, Bestwick, Jonathan, Blauwendraat, Cornelis, Bandres-Ciga, Sara, Heilbron, Karl, Dobson, Ruth, Nalls, Mike A, Singleton, Andrew, Hardy, John, Giovannoni, Gavin, L

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

2020

File:

PDF, 2.03 MB

2020

35

Genome-wide association study of neocortical Lewy-related pathology

Peuralinna, Terhi, Myllykangas, Liisa, Oinas, Minna, Nalls, Mike A., Keage, Hannah A. D., Isoviita, Veli-Matti, Valori, Miko, Polvikoski, Tuomo, Paetau, Anders, Sulkava, Raimo, Ince, Paul G., Zaccai,

Journal:

Annals of Clinical and Translational Neurology

Year:

2015

Language:

english

File:

PDF, 721 KB

english, 2015

36

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

Matthew Traylor, Martin Farrall, Elizabeth G Holliday, Cathie Sudlow, Jemma C Hopewell, Yu-Ching Cheng, Myriam Fornage, M Arfan Ikram, Rainer Malik, Steve Bevan, Unnur Thorsteinsdottir, Mike A Nalls,

Journal:

The Lancet Neurology

Year:

2012

Language:

english

File:

PDF, 1.24 MB

english, 2012

37

CHCHD2 and Parkinson's disease

Jansen, Iris E, Bras, Jose M, Lesage, Suzanne, Schulte, Claudia, Gibbs, J Raphael, Nalls, Mike A, Brice, Alexis, Wood, Nicholas W, Morris, Huw, Hardy, John A, Singleton, Andrew B, Gasser, Thomas, Heut

Journal:

The Lancet Neurology

Year:

2015

Language:

english

File:

PDF, 46 KB

english, 2015

38

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

Nalls, Mike A, McLean, Cory Y, Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J, Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel M, Hardy, John, Gasser, Tho

Journal:

The Lancet Neurology

Year:

2015

Language:

english

File:

PDF, 587 KB

english, 2015

39

Genetic variation at 16q24.2 is associated with small vessel stroke

Traylor, Matthew, Malik, Rainer, Nalls, Mike A., Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B., Langefeld, Carl, Saleheen, Danish, Rost, Natalia S., Yet, Idil, Spector,

Journal:

Annals of Neurology

Year:

2017

Language:

english

File:

PDF, 1.76 MB

english, 2017

40

Establishing the role of rare coding variants in known Parkinson’s disease risk loci

Jansen, Iris E., Gibbs, J Raphael, Nalls, Mike A., Price, T Ryan, Lubbe, Steven, van Rooij, Jeroen, Uitterlinden, André G., Kraaij, Robert, Williams, Nigel M., Brice, Alexis, Hardy, John, Wood, Nichol

Journal:

Neurobiology of Aging

Year:

2017

Language:

english

File:

PDF, 1.47 MB

english, 2017

41

Fine-mapping, Novel Loci Identification, and SNP Association Transferability in a Genome-Wide Association Study of QRS Duration in African Americans

Evans, Daniel S., Avery, Christy L., Nalls, Mike A., Li, Guo, Barnard, John, Smith, Erin N., Tanaka, Toshiko, Butler, Anne M., Buxbaum, Sarah G., Alonso, Alvaro, Arking, Dan E., Berenson, Gerald S., B

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 978 KB

english, 2016

42

Another explanation for apparent epistasis

Wood, Andrew R., Tuke, Marcus A., Nalls, Mike A., Hernandez, Dena G., Bandinelli, Stefania, Singleton, Andrew B., Melzer, David, Ferrucci, Luigi, Frayling, Timothy M., Weedon, Michael N.

Journal:

Year:

2014

Language:

english

File:

PDF, 144 KB

english, 2014

43

Meta-analysis of Correlated Traits via Summary Statistics from GWASs with an Application in Hypertension

Zhu, Xiaofeng, Feng, Tao, Tayo, Bamidele O., Liang, Jingjing, Young, J. Hunter, Franceschini, Nora, Smith, Jennifer A., Yanek, Lisa R., Sun, Yan V., Edwards, Todd L., Chen, Wei, Nalls, Mike, Fox, Ervi

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.80 MB

english, 2015

44

What Success Can Teach Us About Failure: The Plasma Metabolome of Older Adults with Superior Memory and Lessons for Alzheimer’s Disease

Mapstone, Mark, Lin, Feng, Nalls, Mike A., Cheema, Amrita K., Singleton, Andrew B., Fiandaca, Massimo S., Federoff, Howard J.

Journal:

Neurobiology of Aging

Year:

2016

Language:

english

File:

PDF, 1.01 MB

english, 2016

45

Clinical-genetic model predicts incident impulse control disorders in Parkinson's disease

Kraemmer, Julia, Smith, Kara, Weintraub, Daniel, Guillemot, Vincent, Nalls, Mike A, Cormier-Dequaire, Florence, Moszer, Ivan, Brice, Alexis, Singleton, Andrew B, Corvol, Jean-Christophe

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

2016

Language:

english

File:

PDF, 375 KB

english, 2016

46

Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus

Blauwendraat, Cornelis, Bras, Jose M., Nalls, Mike A., Lewis, Patrick A., Hernandez, Dena G., Singleton, Andrew B.

Journal:

Movement Disorders

Year:

2018

Language:

english

File:

PDF, 110 KB

english, 2018

47

Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study

Moore, Ann Zenobia, Hernandez, Dena G., Tanaka, Toshiko, Pilling, Luke C., Nalls, Mike A., Bandinelli, Stefania, Singleton, Andrew B., Ferrucci, Luigi

Journal:

The Journals of Gerontology Series A Biological Sciences and Medical Sciences

Year:

2015

Language:

english

File:

PDF, 804 KB

english, 2015

48

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

Chiò, Adriano, Mora, Gabriele, Sabatelli, Mario, Caponnetto, Claudia, Traynor, Bryan J., Johnson, Janel O., Nalls, Mike A., Calvo, Andrea, Moglia, Cristina, Borghero, Giuseppe, Monsurrò, Maria Rosaria

Journal:

Neurobiology of Aging

Year:

2015

Language:

english

File:

PDF, 218 KB

english, 2015

49

Additional Rare Variant Analysis in Parkinson’s Disease Cases with and Without Known Pathogenic Mutations: Evidence for Oligogenic Inheritance

Lubbe, Steven J., Escott-Price, Valentina, Gibbs, J. Raphael, Nalls, Mike A., Bras, Jose, Price, T. Ryan, Nicolas, Aude, Jansen, Iris E., Mok, Kin Y, Pittman, Alan M., Tomkins, James E., Lewis, Patric

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 226 KB

english, 2016

50

Genetic variability at the PARK16 locus

Tucci, Arianna, Nalls, Mike A, Houlden, Henry, Revesz, Tamas, Singleton, Andrew B, Wood, Nicholas W, Hardy, John, Paisán-Ruiz, Coro

Journal:

European Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 200 KB

english, 2010

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