Pankratz, Nathan D.: search on Z-Library

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1

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia

Nathan Pankratz, Lisa Byder, Cheryl Halter, Alice Rudolph, Clifford W. Shults, P. Michael Conneally, Tatiana Foroud, William C. Nichols

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 69 KB

english, 2006

2

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

3

Candidate pathway-based genetic association study of platinum and platinum–taxane related toxicity in a cohort of primary lung cancer patients

Johnson, Cassandra, Pankratz, Vernon S., Velazquez, Ana I., Aakre, Jeremiah A., Loprinzi, Charles L., Staff, Nathan P., Windebank, Anthony J., Yang, Ping

Journal:

Journal of the Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 401 KB

english, 2015

4

Heritability of Vascular Structure and Function: A Parent–Child Study

Ryder, Justin R., Pankratz, Nathan D., Dengel, Donald R., Pankow, James S., Jacobs, David R., Sinaiko, Alan R., Gooty, Vasu, Steinberger, Julia

Journal:

Journal of the American Heart Association

Year:

2017

Language:

english

File:

PDF, 724 KB

english, 2017

5

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease

Raffield, Laura M., Ulirsch, Jacob C., Naik, Rakhi P., Lessard, Samuel, Handsaker, Robert E., Jain, Deepti, Kang, Hyun M., Pankratz, Nathan, Auer, Paul L., Bao, Erik L., Smith, Joshua D., Lange, Lesli

Journal:

Year:

2018

Language:

english

File:

PDF, 2.14 MB

english, 2018

6

Nearly Half of TP53 Germline Variants Predicted To Be Pathogenic in Patients With Osteosarcoma Are De Novo: A Report From the Childrenâs Oncology Group

Diessner, Brandon J., Pankratz, Nathan, Hooten, Anthony J., Mirabello, Lisa, Sarver, Aaron L., Mills, Lauren J., Malkin, David, Kelley, Ava C., Spector, Logan G.

Journal:

JCO Precision Oncology

Year:

2020

File:

PDF, 575 KB

2020

7

Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2

Nathan Pankratz, Gary W. Beecham, Anita L. DeStefano, Ted M. Dawson, Kimberly F. Doheny, Stewart A. Factor, Taye H. Hamza, Albert Y. Hung, Bradley T. Hyman, Adrian J. Ivinson, Dmitri Krainc, Jeanne C.

Journal:

Annals of Neurology

Year:

2012

Language:

english

File:

PDF, 1017 KB

english, 2012

8

Copy Number Variation in Familial Parkinson Disease

Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N., Sun, Mei, Latourelle, Jeanne C., Wilk, Jemma B., Halter, Cheryl, Doheny, Kimberly F., Gusella, James F., Nichols, William C., Myers, Richard H.

Journal:

Year:

2011

Language:

english

File:

PDF, 637 KB

english, 2011

9

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Fran

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 986 KB

english, 2016

10

Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

Bien, Stephanie A., Pankow, James S., Haessler, Jeffrey, Lu, Yinchang, Pankratz, Nathan, Rohde, Rebecca R., Tamuno, Alfred, Carlson, Christopher S., Schumacher, Fredrick R., Bůžková, Petra, Daviglus,

Journal:

Year:

2017

Language:

english

File:

PDF, 279 KB

english, 2017

11

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

Holzinger, Emily R., Verma, Shefali S., Moore, Carrie B., Hall, Molly, De, Rishika, Gilbert-Diamond, Diane, Lanktree, Matthew B., Pankratz, Nathan, Amuzu, Antoinette, Burt, Amber, Dale, Caroline, Dude

Journal:

Year:

2017

Language:

english

File:

PDF, 1.97 MB

english, 2017

12

Alpha-synuclein and familial Parkinson's disease

Nathan Pankratz, William C. Nichols, Veronika E. Elsaesser, Michael W. Pauciulo, Diane K. Marek, Cheryl A. Halter, Joanne Wojcieszek, Alice Rudolph, Ronald F. Pfeiffer, Tatiana Foroud

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 130 KB

english, 2009

13

Preliminary analysis of copy number variation in the ADNI cohort

Shanker Swaminathan, Sungeun Kim, Li Shen, Shannon L. Risacher, Tatiana Foroud, Nathan Pankratz, Steven G. Potkin, Matthew J. Huentelman, David W. Craig, Michael W. Weiner, Andrew J. Saykin

Journal:

Alzheimer's & Dementia

Year:

2010

Language:

english

File:

PDF, 156 KB

english, 2010

14

The Associations between 6-n-Propylthiouracil (PROP) Intensity and Taste Intensities Differ by TAS2R38 Haplotype

Fischer, Mary E., Cruickshanks, Karen J., Pankow, James S., Pankratz, Nathan, Schubert, Carla R., Huang, Guan-Hua, Klein, Barbara E.K., Klein, Ronald, Pinto, Alex

Journal:

Journal of Nutrigenetics and Nutrigenomics

Year:

2015

Language:

english

File:

PDF, 1.05 MB

english, 2015

15

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease

Hernández-Ramírez, Laura C., Gam, Ryhem, Valdés, Nuria, Lodish, Maya, Pankratz, Nathan, Balsalobre, Aurélio, Gauthier, Yves, Faucz, Fabio R, Trivellin, Giampaolo, Chittiboina, Prashant, Lane, John, Ka

Journal:

Endocrine Related Cancer

Year:

2017

Language:

english

File:

PDF, 2.30 MB

english, 2017

16

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease

Hui, Ken Y., Fernandez-Hernandez, Heriberto, Hu, Jianzhong, Schaffner, Adam, Pankratz, Nathan, Hsu, Nai-Yun, Chuang, Ling-Shiang, Carmi, Shai, Villaverde, Nicole, Li, Xianting, Rivas, Manual, Levine,

Journal:

Science Translational Medicine

Year:

2018

Language:

english

File:

PDF, 1.82 MB

english, 2018

17

Omega-3 Fatty Acids and Genome-wide Interaction Analyses Reveal DPP10 -Pulmonary Function Association

Xu, Jiayi, Gaddis, Nathan C., Bartz, Traci M, Hou, Ruixue, Manichaikul, Ani W, Pankratz, Nathan, Smith, Albert V., Sun, Fangui, Terzikhan, Natalie, Markunas, Christina A., Patchen, Bonnie K., Schu, Ma

Journal:

American Journal of Respiratory and Critical Care Medicine

Year:

2018

Language:

english

File:

PDF, 5.00 MB

english, 2018

18

Issues in association mapping with high-density SNP data and diverse family structures

Heike Bickeböller, Katrina A.B. Goddard, Robert P. Igo Jr., Peter Kraft, Jingky P. Lozano, Nathan Pankratz

Journal:

Genetic Epidemiology

Year:

2007

Language:

english

File:

PDF, 268 KB

english, 2007

19

Chromosome 5 and Parkinson disease

Foroud, Tatiana, Pankratz, Nathan, Martinez, Maria

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 100 KB

english, 2006

20

Preliminary analysis of copy number variation in the ADNI cohort

Shanker Swaminathan, Sungeun Kim, Li Shen, Shannon L. Risacher, Tatiana Foroud, Nathan Pankratz, Steven G. Potkin, Matthew J. Huentelman, David W. Craig, Michael W. Weiner, Andrew J. Saykin

Journal:

Alzheimer's & Dementia

Year:

2010

Language:

english

File:

PDF, 108 KB

english, 2010

21

Rare Nonsynonymous Exonic Variants in Addiction and Behavioral Disinhibition

Vrieze, Scott I., Feng, Shuang, Miller, Michael B., Hicks, Brian M., Pankratz, Nathan, Abecasis, Gonçalo R., Iacono, William G., McGue, Matt

Journal:

Biological Psychiatry

Year:

2014

Language:

english

File:

PDF, 159 KB

english, 2014

22

Parametric Linkage Analysis and Disequilibrium Methods to Identify Loci for Complex Disease

McClintick, Jeanette, Koller, Daniel L., Pankratz, Nathan, Kirkwood, Sandra C., Naughton, Brian, Foroud, Tatiana

Journal:

Genetic Epidemiology

Year:

2001

Language:

english

File:

PDF, 419 KB

english, 2001

23

Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variables

Weng, Lu-Chen, Guan, Weihua, Steffen, Lyn M., Pankow, James S., Pankratz, Nathan, Chen, Ming-Huei, Cushman, Mary, Basu, Saonli, Folsom, Aaron R., Tang, Weihong

Journal:

Thrombosis Research

Year:

2018

Language:

english

File:

PDF, 286 KB

english, 2018

24

Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data

Phillip E. Melton, Nathan Pankratz

Journal:

Genetic Epidemiology

Year:

2011

Language:

english

File:

PDF, 110 KB

english, 2011

25

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle, Anita L. DeStefano, Cheryl Halter, Elizabeth W. Pugh, Kimberly F. Doheny, James F. Gusella, William C. Nichols, Tatiana Foroud, Richard H. Myers,

Journal:

Year:

2009

Language:

english

File:

PDF, 767 KB

english, 2009

26

Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study

Onyeaghala, Guillaume, Lane, John, Pankratz, Nathan, Nelson, Heather H., Thyagarajan, Bharat, Walcheck, Bruce, Anderson, Kristin E., Prizment, Anna E., Parine, Narasimha Reddy

Journal:

Year:

2019

Language:

english

File:

PDF, 663 KB

english, 2019

27

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

William C. Nichols, Diane K. Marek, Michael W. Pauciulo, Nathan Pankratz, Cheryl A. Halter, Alice Rudolph, Clifford W. Shults, Joanne Wojcieszek, Tatiana Foroud

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 66 KB

english, 2007

28

Genetic and Nongenetic Risk Factors for Childhood Cancer

Spector, Logan G., Pankratz, Nathan, Marcotte, Erin L.

Journal:

Pediatric Clinics of North America

Year:

2015

Language:

english

File:

PDF, 680 KB

english, 2015

29

A Genome-Wide Study of Familial Alzheimer’s Disease Supports Additional Candidate Genes: The NIA-LOAD/NCRAD Family Study

Joseph Lee, Rong Cheng, Nathan Pankratz, Ellen Wijsman, Thomas Bird, Tatiana Foroud, Richard Mayeux

Journal:

Alzheimer's & Dementia

Year:

2011

Language:

english

File:

PDF, 54 KB

english, 2011

30

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

Pankratz, Nathan, Schick, Ursula M, Zhou, Yi, Zhou, Wei, Ahluwalia, Tarunveer Singh, Allende, Maria Laura, Auer, Paul L, Bork-Jensen, Jette, Brody, Jennifer A, Chen, Ming-Huei, Clavo, Vinna, Eicher, J

Journal:

Nature Genetics

Year:

2016

Language:

english

File:

PDF, 1.44 MB

english, 2016

31

Hearing Impairment Susceptibility in Elderly Men and the DFNA18 Locus

Garringer, Holly J., Pankratz, Nathan D., Nichols, William C., Reed, Terry

Journal:

Archives of Otolaryngology - Head and Neck Surgery

Year:

2006

Language:

english

File:

PDF, 99 KB

english, 2006

32

Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study

Raffield, Laura M., Ellis, Jaclyn, Olson, Nels C., Duan, Qing, Li, Jin, Durda, Peter, Pankratz, Nathan, Keating, Brendan J., Wassel, Christina L., Cushman, Mary, Wilson, James G., Gross, Myron D., Tra

Journal:

Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 612 KB

english, 2018

33

Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study

Onyeaghala, Guillaume, Lane, John, Pankratz, Nathan, Nelson, Heather H., Thyagarajan, Bharat, Walcheck, Bruce, Anderson, Kristin E., Prizment, Anna E., Parine, Narasimha Reddy

Journal:

Year:

2019

File:

PDF, 663 KB

2019

34

Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population‐based study

Tang, Weihong, Stimson, Mary Rachel, Basu, Saonli, Heckbert, Susan R., Cushman, Mary, Pankow, James S., Folsom, Aaron R., Pankratz, Nathan

Journal:

Journal of Thrombosis and Haemostasis

Year:

2019

Language:

english

File:

PDF, 11.06 MB

english, 2019

35

Non-redundant summary scores applied to the North American Rheumatoid Arthritis Consortium dataset

Pankratz, Nathan D

Journal:

BMC Proceedings

Year:

2009

Language:

english

File:

PDF, 290 KB

english, 2009

36

Genetics of Parkinson disease

Pankratz, Nathan, Foroud, Tatiana

Journal:

Genetics in Medicine

Year:

2007

Language:

english

File:

PDF, 357 KB

english, 2007

37

Voxelwise gene-wide association study (vGeneWAS): Multivariate gene-based association testing in 731 elderly subjects

Derrek P. Hibar, Jason L. Stein, Omid Kohannim, Neda Jahanshad, Andrew J. Saykin, Li Shen, Sungeun Kim, Nathan Pankratz, Tatiana Foroud, Matthew J. Huentelman, Steven G. Potkin, Clifford R. Jack Jr.,

Journal:

Year:

2011

Language:

english

File:

PDF, 1.97 MB

english, 2011

38

A commonly carried allele of the obesity-relatedFTOgene is associated with reduced brain volume in the healthy elderly

April J. Ho, Jason L. Stein, Xue Hua, Suh Lee, Derrek P. Hibar, Alex D. Leow, Ivo D. Dinov, Arthur W. Toga, Andrew J. Saykin, Li Shen, Tatiana Foroud, Nathan Pankratz, Matthew J. Huentelman, David W.

Journal:

Proceedings of the National Academy of Sciences

Year:

2010

Language:

english

File:

PDF, 1.46 MB

english, 2010

39

Association of Mitochondrial DNA Copy Number With Cardiovascular Disease

Ashar, Foram N., Zhang, Yiyi, Longchamps, Ryan J., Lane, John, Moes, Anna, Grove, Megan L., Mychaleckyj, Josyf C., Taylor, Kent D., Coresh, Josef, Rotter, Jerome I., Boerwinkle, Eric, Pankratz, Nathan

Journal:

JAMA Cardiology

Year:

2017

Language:

english

File:

PDF, 247 KB

english, 2017

40

RELATIONSHIP BETWEEN ENVISIA GENOMIC CLASSIFIER AND AN HRCT-DERIVED FIBROTIC INDEX FROM DATA DRIVEN TEXTURE ANALYSIS ON 50 ILD PATIENTS

Humphries, Stephen, Johnson, Marla, Nathan, Steven, Lofaro, Lori, Pankratz, Daniel, Bhorade, Sangeeta, Kennedy, Giulia, Huang, Jing, Lynch, David

Journal:

Year:

2020

File:

PDF, 65 KB

2020

41

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

Fernández-Rhodes, Lindsay, Malinowski, Jennifer R., Wang, Yujie, Tao, Ran, Pankratz, Nathan, Jeff, Janina M., Yoneyama, Sachiko, Carty, Cara L., Setiawan, V. Wendy, Le Marchand, Loic, Haiman, Christop

Journal:

Year:

2018

Language:

english

File:

PDF, 2.08 MB

english, 2018

42

Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease

Nathan Pankratz, Michael W. Pauciulo, Veronika E. Elsaesser, Diane K. Marek, Cheryl A. Halter, Alice Rudolph, Clifford W. Shults, Tatiana Foroud, William C. Nichols

Journal:

Movement Disorders

Year:

2006

Language:

english

File:

PDF, 64 KB

english, 2006

43

The Familial Intracranial Aneurysm (FIA) study protocol

Joseph P Broderick, Laura R Sauerbeck, Tatiana Foroud, John Huston, Nathan Pankratz, Irene Meissner, Robert D Brown

Journal:

BMC Medical Genetics

Year:

2005

Language:

english

File:

PDF, 563 KB

english, 2005

44

Validation of a hybrid approach to standardize immunophenotyping analysis in large population studies: The Health and Retirement Study

Hunter-Schlichting, DeVon, Lane, John, Cole, Benjamin, Flaten, Zachary, Barcelo, Helene, Ramasubramanian, Ramya, Cassidy, Erin, Faul, Jessica, Crimmins, Eileen, Pankratz, Nathan, Thyagarajan, Bharat

Journal:

Scientific Reports

Year:

2020

File:

PDF, 1.29 MB

2020

45

Identification of genes for complex disease using longitudinal phenotypes

Nathan Pankratz, Nitai Mukhopadhyay, Shuguang Huang, Tatiana Foroud, Sandra Close Kirkwood

Journal:

Year:

2003

Language:

english

File:

PDF, 882 KB

english, 2003

46

Voxelwise genome-wide association study (vGWAS)

Jason L. Stein, Xue Hua, Suh Lee, April J. Ho, Alex D. Leow, Arthur W. Toga, Andrew J. Saykin, Li Shen, Tatiana Foroud, Nathan Pankratz, Matthew J. Huentelman, David W. Craig, Jill D. Gerber, April N.

Journal:

Year:

2010

Language:

english

File:

PDF, 2.12 MB

english, 2010

47

Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes

Chidambaram, Manickam, Liju, Samuel, Saboo, Banshi, Sathyavani, Kumpatla, Viswanathan, Vijay, Pankratz, Nathan, Gross, Myron, Mohan, Viswanathan, Radha, Venkatesan

Journal:

Acta Diabetologica

Year:

2016

Language:

english

File:

PDF, 409 KB

english, 2016

48

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Fran

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 57 KB

english, 2016

49

Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium

Bien, Stephanie A., Pankow, James S., Haessler, Jeffrey, Lu, Yinchang N., Pankratz, Nathan, Rohde, Rebecca R., Tamuno, Alfred, Carlson, Christopher S., Schumacher, Fredrick R., Bůžková, Petra, Daviglu

Journal:

Year:

2017

Language:

english

File:

PDF, 844 KB

english, 2017

50

Klinefelter syndrome in males with germ cell tumors: A report from the children’s oncology group

Williams, Lindsay A., Pankratz, Nathan, Lane, John, Krailo, Mark, Roesler, Michelle, Richardson, Michaela, Lindsay Frazier, A., Amatruda, James F., Poynter, Jenny N.

Journal:

Year:

2018

Language:

english

File:

PDF, 412 KB

english, 2018

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