| Year |
Citation |
Score |
| 2023 |
Pankratz N, Cole BR, Beutel KM, Liao KP, Ashe J. Parkinson Disease Genetics Extended to African and Hispanic Ancestries in the VA Million Veteran Program. Neurology. Genetics. 10: e200110. PMID 38130828 DOI: 10.1212/NXG.0000000000200110 |
0.306 |
|
| 2023 |
Huffman JE, Nicolas J, Hahn J, Heath AS, Raffield LM, Yanek LR, Brody JA, Thibord F, Almasy L, Bartz TM, Bielak LF, Bowler RP, Carrasquilla GD, Chasman DI, Chen MH, ... ... Pankratz N, et al. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Medrxiv : the Preprint Server For Health Sciences. PMID 37398003 DOI: 10.1101/2023.06.07.23291095 |
0.327 |
|
| 2022 |
Pankratz N, Wei P, Brody JA, Chen MH, Vries PS, Huffman JE, Stimson MR, Auer PL, Boerwinkle E, Cushman M, Maat MPM, Folsom AR, Franco OH, Gibbs RA, Haagenson KK, et al. Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Human Molecular Genetics. PMID 35552711 DOI: 10.1093/hmg/ddac100 |
0.302 |
|
| 2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Pankratz N, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.332 |
|
| 2021 |
Mikhaylova AV, McHugh CP, Polfus LM, Raffield LM, Boorgula MP, Blackwell TW, Brody JA, Broome J, Chami N, Chen MH, Conomos MP, Cox C, Curran JE, Daya M, Ekunwe L, ... ... Pankratz N, et al. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 34582791 DOI: 10.1016/j.ajhg.2021.08.007 |
0.322 |
|
| 2021 |
Hu Y, Stilp AM, McHugh CP, Rao S, Jai D, Zheng X, Lane J, Méric de Bellefon S, Raffield LM, Chen MH, Yanek LR, Wheeler M, Yao Y, Ren C, Broome J, ... ... Pankratz N, et al. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 33887194 DOI: 10.1016/j.ajhg.2021.04.003 |
0.327 |
|
| 2020 |
Vuckovic D, Bao EL, Akbari P, Lareau CA, Mousas A, Jiang T, Chen MH, Raffield LM, Tardaguila M, Huffman JE, Ritchie SC, Megy K, Ponstingl H, Penkett CJ, Albers PK, ... ... Pankratz N, et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 182: 1214-1231.e11. PMID 32888494 DOI: 10.1016/J.Cell.2020.08.008 |
0.362 |
|
| 2020 |
Chen MH, Raffield LM, Mousas A, Sakaue S, Huffman JE, Moscati A, Trivedi B, Jiang T, Akbari P, Vuckovic D, Bao EL, Zhong X, Manansala R, Laplante V, Chen M, ... ... Pankratz N, et al. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Cell. 182: 1198-1213.e14. PMID 32888493 DOI: 10.1016/J.Cell.2020.06.045 |
0.366 |
|
| 2020 |
Martínez de LaPiscina I, Hernández-Ramírez LC, Portillo N, Gómez-Gila AL, Urrutia I, Martínez-Salazar R, García-Castaño A, Aguayo A, Rica I, Gaztambide S, Faucz FR, Keil MF, Lodish MB, Quezado M, Pankratz N, et al. Rare Germline Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? Frontiers in Endocrinology. 11: 433. PMID 32714280 DOI: 10.3389/Fendo.2020.00433 |
0.375 |
|
| 2020 |
Chasseloup F, Pankratz N, Lane J, Faucz FR, Keil MF, Chittiboina P, Kay DM, Hussein Tayeb T, Stratakis CA, Mills JL, Hernández-Ramírez LC. Germline CDKN1B loss-of-function variants cause pediatric Cushing's disease with or without an MEN4 phenotype. The Journal of Clinical Endocrinology and Metabolism. PMID 32232325 DOI: 10.1210/Clinem/Dgaa160 |
0.337 |
|
| 2020 |
Mirabello L, Zhu B, Koster R, Karlins E, Dean M, Yeager M, Gianferante M, Spector LG, Morton LM, Karyadi D, Robison LL, Armstrong GT, Bhatia S, Song L, Pankratz N, et al. Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. Jama Oncology. PMID 32191290 DOI: 10.1001/Jamaoncol.2020.0197 |
0.319 |
|
| 2020 |
Longchamps RJ, Castellani CA, Yang SY, Newcomb CE, Sumpter JA, Lane J, Grove ML, Guallar E, Pankratz N, Taylor KD, Rotter JI, Boerwinkle E, Arking DE. Evaluation of mitochondrial DNA copy number estimation techniques. Plos One. 15: e0228166. PMID 32004343 DOI: 10.1371/Journal.Pone.0228166 |
0.333 |
|
| 2020 |
McSweeney ST, Prizment A, Pankratz N, Joshu CE, Platz EA, Ryan CJ. Association of polymorphisms in androgen production, uptake, and conversion chain (APUC) genes with mortality of prostate cancer patients. Journal of Clinical Oncology. 38: 5528-5528. DOI: 10.1200/Jco.2020.38.15_Suppl.5528 |
0.369 |
|
| 2019 |
Raffield LM, Iyengar AK, Wang B, Gaynor SM, Spracklen CN, Zhong X, Kowalski MH, Salimi S, Polfus LM, Benjamin EJ, Bis JC, Bowler R, Cade BE, Choi WJ, Comellas AP, ... ... Pankratz N, et al. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. American Journal of Human Genetics. PMID 31883642 DOI: 10.1016/J.Ajhg.2019.12.002 |
0.405 |
|
| 2019 |
Kowalski MH, Qian H, Hou Z, Rosen JD, Tapia AL, Shan Y, Jain D, Argos M, Arnett DK, Avery C, Barnes KC, Becker LC, Bien SA, Bis JC, Blangero J, ... ... Pankratz N, et al. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Plos Genetics. 15: e1008500. PMID 31869403 DOI: 10.1371/Journal.Pgen.1008500 |
0.41 |
|
| 2019 |
Tang W, Stimson MR, Basu S, Heckbert SR, Cushman M, Pankow JS, Folsom AR, Pankratz N. Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study. Journal of Thrombosis and Haemostasis : Jth. PMID 31680443 DOI: 10.1111/Jth.14676 |
0.373 |
|
| 2019 |
Tang W, Saratzis A, Pattee J, Smith J, Pankratz N, Leavy OC, Guan W, Dudbridge F, Pankow JS, Kitas GD, Lutsey PL, Bown MJ. Replication of Newly Identified Genetic Associations Between Abdominal Aortic Aneurysm and SMYD2, LINC00540, PCIF1/MMP9/ZNF335, and ERG. European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society For Vascular Surgery. PMID 31680049 DOI: 10.1016/J.Ejvs.2019.02.017 |
0.372 |
|
| 2019 |
Nagtegaal AP, Broer L, Zilhao NR, Jakobsdottir J, Bishop CE, Brumat M, Christiansen MW, Cocca M, Gao Y, Heard-Costa NL, Evans DS, Pankratz N, Pratt SR, Price TR, Spankovich C, et al. Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. Scientific Reports. 9: 15192. PMID 31645637 DOI: 10.1038/S41598-019-51630-X |
0.348 |
|
| 2019 |
Best LG, Balakrishnan P, Cole SA, Haack K, Kocarnik JM, Pankratz N, Anderson MZ, Franceschini N, Howard BV, Lee ET, North KE, Umans JG, Yracheta JM, Navas-Acien A, Voruganti VS. Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study. Plos One. 14: e0223574. PMID 31622379 DOI: 10.1371/Journal.Pone.0223574 |
0.408 |
|
| 2019 |
Fang G, Wang W, Paunic V, Heydari H, Costanzo M, Liu X, Liu X, VanderSluis B, Oately B, Steinbach M, Van Ness B, Schadt EE, Pankratz ND, Boone C, Kumar V, et al. Discovering genetic interactions bridging pathways in genome-wide association studies. Nature Communications. 10: 4274. PMID 31537791 DOI: 10.1038/S41467-019-12131-7 |
0.393 |
|
| 2019 |
Lindstrom S, Wang L, Smith EN, Gordon W, van Hylckama Vlieg A, de Andrade M, Brody JA, Pattee JW, Haessler J, Brumpton BM, Chasman DI, Suchon P, Chen MH, Turman C, Germain M, ... ... Pankratz N, et al. Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. Blood. PMID 31420334 DOI: 10.1182/Blood.2019000435 |
0.425 |
|
| 2019 |
Onyeaghala G, Lane J, Pankratz N, Nelson HH, Thyagarajan B, Walcheck B, Anderson KE, Prizment AE. Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study. Plos One. 14: e0217868. PMID 31166958 DOI: 10.1371/Journal.Pone.0217868 |
0.314 |
|
| 2019 |
Ward-Caviness CK, de Vries PS, Wiggins KL, Huffman JE, Yanek LR, Bielak LF, Giulianini F, Guo X, Kleber ME, Kacprowski T, Groß S, Petersman A, Davey Smith G, Hartwig FP, Bowden J, ... ... Pankratz N, et al. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. Plos One. 14: e0216222. PMID 31075152 DOI: 10.1371/Journal.Pone.0216222 |
0.322 |
|
| 2019 |
Lindström S, Brody JA, Turman C, Germain M, Bartz TM, Smith EN, Chen MH, Puurunen M, Chasman D, Hassler J, Pankratz N, Basu S, Guan W, Gyorgy B, Ibrahim M, et al. A large-scale exome array analysis of venous thromboembolism. Genetic Epidemiology. PMID 30659681 DOI: 10.1002/Gepi.22187 |
0.431 |
|
| 2019 |
de Vries PS, Sabater-Lleal M, Huffman JE, Marten J, Song C, Pankratz N, Bartz TM, de Haan HG, Delgado GE, Eicher JD, Martinez-Perez A, Ward-Caviness CK, Brody JA, Chen MH, de Maat MPM, et al. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. Blood. PMID 30642921 DOI: 10.1182/Blood-2018-05-849240 |
0.363 |
|
| 2019 |
Hernández-Ramírez L, Chasseloup F, Faucz F, Lodish M, Pankratz N, Chittiboina P, Lane J, Kay D, Mills J, Stratakis C. OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Or24-6 |
0.33 |
|
| 2018 |
Tatsi C, Pankratz N, Lane J, Faucz FR, Hernández-Ramírez LC, Keil M, Trivellin G, Chittiboina P, Mills JL, Stratakis CA, Lodish MB. Large genomic aberrations in corticotropinomas are associated with greater aggressiveness. The Journal of Clinical Endocrinology and Metabolism. PMID 30597087 DOI: 10.1210/Jc.2018-02164 |
0.343 |
|
| 2018 |
Sabater-Lleal M, Huffman JE, de Vries PS, Marten J, Mastrangelo MA, Song C, Pankratz N, Ward-Caviness CK, Yanek LR, Trompet S, Delgado GE, Guo X, Bartz TM, Martinez-Perez A, Germain M, et al. Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. Circulation. PMID 30586737 DOI: 10.1161/Circulationaha.118.034532 |
0.337 |
|
| 2018 |
Polfus LM, Raffield LM, Wheeler MM, Tracy RP, Lange LA, Lettre G, Miller A, Correa A, Bowler RP, Bis JC, Salimi S, Jenny NS, Pankratz N, Wang B, Preuss MH, et al. Whole genome sequence association with E-selectin levels reveals Loss-of-function variant in African Americans. Human Molecular Genetics. PMID 30307499 DOI: 10.1093/Hmg/Ddy360 |
0.378 |
|
| 2018 |
Fernández-Rhodes L, Malinowski JR, Wang Y, Tao R, Pankratz N, Jeff JM, Yoneyama S, Carty CL, Setiawan VW, Le Marchand L, Haiman C, Corbett S, Demerath E, Heiss G, Gross M, et al. 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. Plos One. 13: e0200486. PMID 30044860 DOI: 10.1371/Journal.Pone.0200486 |
0.386 |
|
| 2018 |
Weng LC, Guan W, Steffen LM, Pankow JS, Pankratz N, Chen MH, Cushman M, Basu S, Folsom AR, Tang W. Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variables. Thrombosis Research. 168: 53-59. PMID 29902632 DOI: 10.1016/J.Thromres.2018.05.032 |
0.332 |
|
| 2018 |
Kocarnik JM, Richard M, Graff M, Haessler J, Bien S, Carlson C, Carty CL, Reiner AP, Avery CL, Ballantyne CM, LaCroix AZ, Assimes TL, Barbalic M, Pankratz N, Tang W, et al. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. Human Molecular Genetics. PMID 29878111 DOI: 10.1093/Hmg/Ddy211 |
0.331 |
|
| 2018 |
Raffield LM, Ellis J, Olson NC, Duan Q, Li J, Durda P, Pankratz N, Keating BJ, Wassel CL, Cushman M, Wilson JG, Gross MD, Tracy RP, Rich SS, Reiner AP, et al. 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. Journal of Human Genetics. PMID 29321517 DOI: 10.1038/S10038-017-0384-9 |
0.404 |
|
| 2018 |
Hui KY, Fernandez-Hernandez H, Hu J, Schaffner A, Pankratz N, Hsu NY, Chuang LS, Carmi S, Villaverde N, Li X, Rivas M, Levine AP, Bao X, Labrias PR, Haritunians T, et al. Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Science Translational Medicine. 10. PMID 29321258 DOI: 10.1126/Scitranslmed.Aai7795 |
0.54 |
|
| 2018 |
Onyeaghala GC, Lane J, Pankratz N, Nelson HH, Thyagarajan B, Anderson KE, Prizment AE. Abstract 1219: Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study Cancer Research. 78: 1219-1219. DOI: 10.1158/1538-7445.Am2018-1219 |
0.329 |
|
| 2017 |
Hernández-Ramírez LC, Tatsi C, Lodish MB, Faucz FR, Pankratz N, Chittiboina P, Lane J, Kay DM, Valdés N, Dimopoulos A, Mills JL, Stratakis CA. Corticotropinoma as a Component of Carney Complex. Journal of the Endocrine Society. 1: 918-925. PMID 29264542 DOI: 10.1210/Js.2017-00231 |
0.349 |
|
| 2017 |
Boghossian NS, Sicko RJ, Giannakou A, Dimopoulos A, Caggana M, Tsai MY, Yeung EH, Pankratz N, Cole BR, Romitti PA, Browne ML, Fan R, Liu A, Kay DM, Mills JL. Rare copy number variants identified in prune belly syndrome. European Journal of Medical Genetics. PMID 29174092 DOI: 10.1016/J.Ejmg.2017.11.008 |
0.397 |
|
| 2017 |
Bien SA, Pankow JS, Haessler J, Lu Y, Pankratz N, Rohde RR, Tamuno A, Carlson CS, Schumacher FR, Bůžková P, Daviglus ML, Lim U, Fornage M, Fernandez-Rhodes L, Avilés-Santa L, et al. Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID 29038867 DOI: 10.1007/S00125-017-4476-Z |
0.323 |
|
| 2017 |
Bien SA, Pankow JS, Haessler J, Lu YN, Pankratz N, Rohde RR, Tamuno A, Carlson CS, Schumacher FR, Bůžková P, Daviglus ML, Lim U, Fornage M, Fernandez-Rhodes L, Avilés-Santa L, et al. Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium. Diabetologia. PMID 28905132 DOI: 10.1007/S00125-017-4405-1 |
0.356 |
|
| 2017 |
Folsom AR, Roetker NS, Kelley ST, Tang W, Pankratz N. Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans. Blood. PMID 28619983 DOI: 10.1182/Blood-2017-03-771329 |
0.34 |
|
| 2017 |
Hernández-Ramírez LC, Gam R, Valdés N, Lodish M, Pankratz N, Balsalobre A, Gauthier Y, Faucz FR, Trivellin G, Chittiboina P, Lane J, Kay DM, Dimopoulou A, Gaillard S, Neou M, et al. Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease. Endocrine-Related Cancer. PMID 28533356 DOI: 10.1530/Erc-17-0131 |
0.337 |
|
| 2017 |
Faucz FR, Tirosh A, Tatsi C, Berthon A, Hernández-Ramírez LC, Settas N, Angelousi A, Correa R, Papadakis GZ, Chittiboina P, Quezado M, Pankratz N, Lane J, Dimopoulos A, Mills JL, et al. Somatic USP8 gene mutations are a common cause of pediatric Cushing disease. The Journal of Clinical Endocrinology and Metabolism. PMID 28505279 DOI: 10.1210/Jc.2017-00161 |
0.376 |
|
| 2017 |
Hodonsky CJ, Jain D, Schick UM, Morrison JV, Brown L, McHugh CP, Schurmann C, Chen DD, Liu YM, Auer PL, Laurie CA, Taylor KD, Browning BL, Li Y, Papanicolaou G, ... ... Pankratz N, et al. Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Plos Genetics. 13: e1006760. PMID 28453575 DOI: 10.1371/Journal.Pgen.1006760 |
0.409 |
|
| 2017 |
Marcotte EL, Pankratz N, Amatruda JF, Frazier AL, Krailo M, Davies S, Starr JR, Ching CL, Roesler M, Langer E, Hallstrom C, Hooten AJ, Poynter JN. Variants in BAK1, SPRY4, and GAB2 are Associated with Pediatric Germ Cell Tumors: A Report from the Children's Oncology Group. Genes, Chromosomes & Cancer. PMID 28295819 DOI: 10.1002/Gcc.22457 |
0.382 |
|
| 2017 |
Pankow JS, Tang W, Pankratz N, Guan W, Weng LC, Cushman M, Boerwinkle E, Folsom AR. Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities). Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 28082259 DOI: 10.1161/Atvbaha.116.308109 |
0.338 |
|
| 2016 |
Yoneyama S, Yao J, Guo X, Fernandez-Rhodes L, Lim U, Boston J, Buzková P, Carlson CS, Cheng I, Cochran B, Cooper R, Ehret G, Fornage M, Gong J, Gross M, ... ... Pankratz N, et al. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations. International Journal of Obesity (2005). PMID 27867202 DOI: 10.1038/Ijo.2016.207 |
0.344 |
|
| 2016 |
Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen MH, Auer PL, Floyd JS, Huang J, Lange L, van Rooij FJ, Gibbs RA, Metcalf G, Muzny D, et al. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 785. PMID 27588453 DOI: 10.1016/J.Ajhg.2016.08.002 |
0.346 |
|
| 2016 |
Chidambaram M, Liju S, Saboo B, Sathyavani K, Viswanathan V, Pankratz N, Gross M, Mohan V, Radha V. Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes. Acta Diabetologica. PMID 27488727 DOI: 10.1007/S00592-016-0889-2 |
0.302 |
|
| 2016 |
Polfus LM, Khajuria RK, Schick UM, Pankratz N, Pazoki R, Brody JA, Chen MH, Auer PL, Floyd JS, Huang J, Lange L, van Rooij FJ, Gibbs RA, Metcalf G, Muzny D, et al. Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 481-488. PMID 27486782 DOI: 10.1016/J.Ajhg.2016.06.016 |
0.368 |
|
| 2016 |
Tajuddin SM, Schick UM, Eicher JD, Chami N, Giri A, Brody JA, Hill WD, Kacprowski T, Li J, Lyytikäinen LP, Manichaikul A, Mihailov E, O'Donoghue ML, Pankratz N, Pazoki R, et al. Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases. American Journal of Human Genetics. PMID 27346689 DOI: 10.1016/J.Ajhg.2016.05.003 |
0.415 |
|
| 2016 |
Eicher JD, Chami N, Kacprowski T, Nomura A, Chen MH, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N, Polfus L, Schurmann C, Giri A, Brody JA, Lange LA, et al. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. American Journal of Human Genetics. PMID 27346686 DOI: 10.1016/J.Ajhg.2016.05.005 |
0.353 |
|
| 2016 |
Chami N, Chen MH, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, Kacprowski T, Schick UM, Nomura A, Giri A, Lessard S, Brody JA, Schurmann C, Pankratz N, et al. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. American Journal of Human Genetics. PMID 27346685 DOI: 10.1016/J.Ajhg.2016.05.007 |
0.441 |
|
| 2016 |
Tin A, Grams ME, Ashar FN, Lane JA, Rosenberg AZ, Grove ML, Boerwinkle E, Selvin E, Coresh J, Pankratz N, Arking DE. Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study. Journal of the American Society of Nephrology : Jasn. PMID 26794963 DOI: 10.1681/Asn.2015060661 |
0.312 |
|
| 2016 |
Marcotte EL, Pankratz N, Amatruda J, Frazier AL, Krailo M, Davies S, Starr J, Langer E, Hallstrom C, Hooten A, Poynter JN. Abstract LB-374: Variants in BAK1 and SPRY4 are associated with pediatric germ cell tumors Cancer Research. 76. DOI: 10.1158/1538-7445.Am2016-Lb-374 |
0.378 |
|
| 2016 |
Hui K, Fernandez-Hernandez H, Hu J, Pankratz N, Rivas M, Carmi S, Haritunians T, Atzmon G, Brant S, Daly M, Duerr R, McGovern D, Ostrer H, Rioux J, Silverberg M, et al. P-175 Pleiotropic Effects of Novel Functional LRRK2 Variation on Crohnʼs Disease and Parkinsonʼs Disease Risk Inflammatory Bowel Diseases. 22: S62-S63. DOI: 10.1097/01.Mib.0000480302.17090.47 |
0.479 |
|
| 2015 |
Boghossian NS, Sicko RJ, Kay DM, Rigler SL, Caggana M, Tsai MY, Yeung EH, Pankratz N, Cole BR, Druschel CM, Romitti PA, Browne ML, Fan R, Liu A, Brody LC, et al. Rare copy number variants implicated in posterior urethral valves. American Journal of Medical Genetics. Part A. PMID 26663319 DOI: 10.1002/Ajmg.A.37493 |
0.413 |
|
| 2015 |
Huffman JE, de Vries PS, Morrison AC, Sabater-Lleal M, Kacprowski T, Auer PL, Brody JA, Chasman DI, Chen MH, Guo X, Lin LA, Marioni RE, Müller-Nurasyid M, Yanek LR, Pankratz N, et al. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood. 126: e19-29. PMID 26105150 DOI: 10.1182/Blood-2015-02-624551 |
0.399 |
|
| 2015 |
Mirabello L, Koster R, Moriarity BS, Spector LG, Meltzer PS, Gary J, Machiela MJ, Pankratz N, Panagiotou OA, Largaespada D, Wang Z, Gastier-Foster JM, Gorlick R, Khanna C, Caminada de Toledo SR, et al. A genome-wide scan identifies variants in NFIB associated with metastasis in patients with osteosarcoma. Cancer Discovery. PMID 26084801 DOI: 10.1158/2159-8290.Cd-15-0125 |
0.408 |
|
| 2015 |
Männik K, Mägi R, Macé A, Cole B, Guyatt AL, Shihab HA, Maillard AM, Alavere H, Kolk A, Reigo A, Mihailov E, Leitsalu L, Ferreira AM, Nõukas M, Teumer A, ... ... Pankratz N, et al. Copy number variations and cognitive phenotypes in unselected populations. Jama. 313: 2044-54. PMID 26010633 DOI: 10.1097/01.Ogx.0000471594.65931.90 |
0.367 |
|
| 2015 |
Nalls MA, Bras J, Hernandez DG, Keller MF, Majounie E, Renton AE, Saad M, Jansen I, Guerreiro R, Lubbe S, Plagnol V, Gibbs JR, Schulte C, Pankratz N, Sutherland M, et al. NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases. Neurobiology of Aging. 36: 1605.e7-12. PMID 25444595 DOI: 10.1016/J.Neurobiolaging.2014.07.028 |
0.424 |
|
| 2015 |
Spector LG, Pankratz N, Marcotte EL. Genetic and nongenetic risk factors for childhood cancer. Pediatric Clinics of North America. 62: 11-25. PMID 25435109 DOI: 10.1016/J.Pcl.2014.09.013 |
0.322 |
|
| 2015 |
Schick UM, Auer PL, Bis JC, Lin H, Wei P, Pankratz N, Lange LA, Brody J, Stitziel NO, Kim DS, Carlson CS, Fornage M, Haessler J, Hsu L, Jackson RD, et al. Association of exome sequences with plasma C-reactive protein levels in >9000 participants. Human Molecular Genetics. 24: 559-71. PMID 25187575 DOI: 10.1093/Hmg/Ddu450 |
0.419 |
|
| 2014 |
Vrieze SI, Malone SM, Pankratz N, Vaidyanathan U, Miller MB, Kang HM, McGue M, Abecasis G, Iacono WG. Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes. Psychophysiology. 51: 1300-8. PMID 25387709 DOI: 10.1111/Psyp.12349 |
0.407 |
|
| 2014 |
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics. 46: 989-93. PMID 25064009 DOI: 10.1038/Ng.3043 |
0.577 |
|
| 2014 |
Kocarnik JM, Pendergrass SA, Carty CL, Pankow JS, Schumacher FR, Cheng I, Durda P, Ambite JL, Deelman E, Cook NR, Liu S, Wactawski-Wende J, Hutter C, Brown-Gentry K, Wilson S, ... ... Pankratz N, et al. Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study. Circulation. Cardiovascular Genetics. 7: 178-88. PMID 24622110 DOI: 10.1161/Circgenetics.113.000173 |
0.391 |
|
| 2014 |
Tragante V, Barnes MR, Ganesh SK, Lanktree MB, Guo W, Franceschini N, Smith EN, Johnson T, Holmes MV, Padmanabhan S, Karczewski KJ, Almoguera B, Barnard J, Baumert J, Chang YP, ... ... Pankratz N, et al. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. American Journal of Human Genetics. 94: 349-60. PMID 24560520 DOI: 10.1016/J.Ajhg.2013.12.016 |
0.381 |
|
| 2014 |
Kirkpatrick RM, McGue M, Iacono WG, Miller MB, Basu S, Pankratz N. Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association. Intelligence. 42: 98-106. PMID 24497650 DOI: 10.1016/J.Intell.2013.11.005 |
0.435 |
|
| 2014 |
Vrieze SI, Feng S, Miller MB, Hicks BM, Pankratz N, Abecasis GR, Iacono WG, McGue M. Rare nonsynonymous exonic variants in addiction and behavioral disinhibition. Biological Psychiatry. 75: 783-9. PMID 24094508 DOI: 10.1016/J.Biopsych.2013.08.027 |
0.338 |
|
| 2014 |
Linabery A, Grufferman S, Poynter JN, Ross JA, Spector LG, Kelly KM, Iacono W, McGue M, Pankratz N. Variants in PVT1 are Associated with Susceptibility for Hodgkin Lymphoma in Children and Adolescents: A Children’s Oncology Group Study Blood. 124: 2950-2950. DOI: 10.1182/Blood.V124.21.2950.2950 |
0.381 |
|
| 2013 |
Gong J, Schumacher F, Lim U, Hindorff LA, Haessler J, Buyske S, Carlson CS, Rosse S, Bůžková P, Fornage M, Gross M, Pankratz N, Pankow JS, Schreiner PJ, Cooper R, et al. Fine Mapping and Identification of BMI Loci in African Americans. American Journal of Human Genetics. 93: 661-71. PMID 24094743 DOI: 10.1016/J.Ajhg.2013.08.012 |
0.401 |
|
| 2013 |
Raynor LA, Pankratz N, Spector LG. An analysis of measures of effect size by age of onset in cancer genomewide association studies. Genes, Chromosomes & Cancer. 52: 855-9. PMID 23765633 DOI: 10.1002/Gcc.22081 |
0.317 |
|
| 2013 |
Tang W, Teichert M, Chasman DI, Heit JA, Morange PE, Li G, Pankratz N, Leebeek FW, Paré G, de Andrade M, Tzourio C, Psaty BM, Basu S, Ruiter R, Rose L, et al. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Genetic Epidemiology. 37: 512-21. PMID 23650146 DOI: 10.1002/Gepi.21731 |
0.422 |
|
| 2013 |
Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, ... ... Pankratz N, et al. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. Jama Neurology. 70: 727-35. PMID 23588557 DOI: 10.1001/Jamaneurol.2013.1925 |
0.56 |
|
| 2012 |
Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, ... ... Pankratz N, et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics. 91: 823-38. PMID 23063622 DOI: 10.1016/J.Ajhg.2012.08.032 |
0.35 |
|
| 2012 |
Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. Plos Genetics. 8: e1002794. PMID 22761592 DOI: 10.1371/Journal.Pgen.1002794 |
0.577 |
|
| 2012 |
Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/Ana.22687 |
0.577 |
|
| 2012 |
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, ... ... Pankratz N, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548 |
0.612 |
|
| 2012 |
Lanktree M, Guo Y, Murtaza M, Glessner J, Bailey S, Onland-Moret N, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson C, Klopp N, Baumert J, Padmanabhan S, ... Pankratz N, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height The American Journal of Human Genetics. 90: 1116-1117. DOI: 10.1016/J.Ajhg.2012.05.017 |
0.367 |
|
| 2011 |
Ghosh S, Bickeböller H, Bailey J, Bailey-Wilson JE, Cantor R, Culverhouse R, Daw W, Destefano AL, Engelman CD, Hinrichs A, Houwing-Duistermaat J, König IR, Kent J, Laird N, Pankratz N, et al. Identifying rare variants from exome scans: the GAW17 experience. Bmc Proceedings. 5: S1. PMID 22373325 DOI: 10.1186/1753-6561-5-S9-S1 |
0.356 |
|
| 2011 |
Melton PE, Pankratz N. Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data. Genetic Epidemiology. 35: S67-73. PMID 22128062 DOI: 10.1002/Gepi.20653 |
0.408 |
|
| 2011 |
Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, ... ... Pankratz N, et al. Translation initiator EIF4G1 mutations in familial Parkinson disease. American Journal of Human Genetics. 89: 398-406. PMID 21907011 DOI: 10.1016/J.Ajhg.2011.08.009 |
0.496 |
|
| 2011 |
Pankratz N, Dumitriu A, Hetrick KN, Sun M, Latourelle JC, Wilk JB, Halter C, Doheny KF, Gusella JF, Nichols WC, Myers RH, Foroud T, DeStefano AL. Copy number variation in familial Parkinson disease. Plos One. 6: e20988. PMID 21829596 DOI: 10.1371/Journal.Pone.0020988 |
0.605 |
|
| 2011 |
Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T. Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 2039-44. PMID 21661047 DOI: 10.1002/Mds.23781 |
0.57 |
|
| 2011 |
Swaminathan S, Kim S, Shen L, Risacher SL, Foroud T, Pankratz N, Potkin SG, Huentelman MJ, Craig DW, Weiner MW, Saykin AJ, The Alzheimer's Disease Neuroimaging Initiative Adni. Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. International Journal of Alzheimer's Disease. 2011: 729478. PMID 21660214 DOI: 10.4061/2011/729478 |
0.511 |
|
| 2011 |
Hibar DP, Stein JL, Kohannim O, Jahanshad N, Saykin AJ, Shen L, Kim S, Pankratz N, Foroud T, Huentelman MJ, Potkin SG, Jack CR, Weiner MW, Toga AW, Thompson PM, et al. Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Neuroimage. 56: 1875-91. PMID 21497199 DOI: 10.1016/J.Neuroimage.2011.03.077 |
0.539 |
|
| 2011 |
Wijsman EM, Pankratz ND, Choi Y, Rothstein JH, Faber KM, Cheng R, Lee JH, Bird TD, Bennett DA, Diaz-Arrastia R, Goate AM, Farlow M, Ghetti B, Sweet RA, Foroud TM, et al. Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. Plos Genetics. 7: e1001308. PMID 21379329 DOI: 10.1371/Journal.Pgen.1001308 |
0.565 |
|
| 2011 |
Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... Pankratz N, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/J.Ajhg.2010.11.007 |
0.44 |
|
| 2011 |
Lee J, Cheng R, Pankratz N, Wijsman E, Bird T, Foroud T, Mayeux R. A Genome-Wide Study of Familial Alzheimer’s Disease Supports Additional Candidate Genes: The NIA-LOAD/NCRAD Family Study Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.524 |
0.5 |
|
| 2010 |
Ho AJ, Stein JL, Hua X, Lee S, Hibar DP, Leow AD, Dinov ID, Toga AW, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, et al. A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly. Proceedings of the National Academy of Sciences of the United States of America. 107: 8404-9. PMID 20404173 DOI: 10.1073/Pnas.0910878107 |
0.47 |
|
| 2010 |
Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T. Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease. Bmc Medical Genetics. 11: 53. PMID 20356410 DOI: 10.1186/1471-2350-11-53 |
0.562 |
|
| 2010 |
Stein JL, Hua X, Morra JH, Lee S, Hibar DP, Ho AJ, Leow AD, Toga AW, Sul JH, Kang HM, Eskin E, Saykin AJ, Shen L, Foroud T, Pankratz N, et al. Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage. 51: 542-54. PMID 20197096 DOI: 10.1016/J.Neuroimage.2010.02.068 |
0.54 |
|
| 2010 |
Stein JL, Hua X, Lee S, Ho AJ, Leow AD, Toga AW, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, et al. Voxelwise genome-wide association study (vGWAS). Neuroimage. 53: 1160-74. PMID 20171287 DOI: 10.1016/J.Neuroimage.2010.02.032 |
0.535 |
|
| 2010 |
Shen L, Kim S, Risacher SL, Nho K, Swaminathan S, West JD, Foroud T, Pankratz N, Moore JH, Sloan CD, Huentelman MJ, Craig DW, Dechairo BM, Potkin SG, Jack CR, et al. Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. Neuroimage. 53: 1051-63. PMID 20100581 DOI: 10.1016/J.Neuroimage.2010.01.042 |
0.552 |
|
| 2010 |
Swaminathan S, Kim S, Shen L, Risacher SL, Foroud T, Pankratz N, Potkin SG, Huentelman MJ, Craig DW, Weiner MW, Saykin AJ. Preliminary analysis of copy number variation in the ADNI cohort Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.050 |
0.463 |
|
| 2009 |
Pankratz ND. Non-redundant summary scores applied to the North American Rheumatoid Arthritis Consortium dataset. Bmc Proceedings. 3: S39. PMID 20018030 DOI: 10.1186/1753-6561-3-S7-S39 |
0.395 |
|
| 2009 |
Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T. Genomewide association study for onset age in Parkinson disease. Bmc Medical Genetics. 10: 98. PMID 19772629 DOI: 10.1186/1471-2350-10-98 |
0.607 |
|
| 2009 |
Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Marder KS, Foroud T, Nichols WC. Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. Neurology. 73: 279-86. PMID 19636047 DOI: 10.1212/Wnl.0B013E3181Af7A33 |
0.55 |
|
| 2009 |
Pankratz N, Nichols WC, Elsaesser VE, Pauciulo MW, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Pfeiffer RF, Foroud T. Alpha-synuclein and familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1125-31. PMID 19412953 DOI: 10.1002/Mds.22524 |
0.583 |
|
| 2009 |
Nichols WC, Kissell DK, Pankratz N, Pauciulo MW, Elsaesser VE, Clark KA, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T. Variation in GIGYF2 is not associated with Parkinson disease. Neurology. 72: 1886-92. PMID 19279319 DOI: 10.1212/01.Wnl.0000346517.98982.1B |
0.587 |
|
| 2009 |
Nichols WC, Pankratz N, Marek DK, Pauciulo MW, Elsaesser VE, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T. Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset. Neurology. 72: 310-6. PMID 18987351 DOI: 10.1212/01.Wnl.0000327823.81237.D1 |
0.577 |
|
| 2009 |
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Human Genetics. 124: 593-605. PMID 18985386 DOI: 10.1007/S00439-008-0582-9 |
0.588 |
|
| 2008 |
Pankratz N, Marder KS, Halter CA, Rudolph A, Shults CW, Nichols WC, Foroud T. Clinical correlates of depressive symptoms in familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 2216-23. PMID 18785635 DOI: 10.1002/Mds.22285 |
0.47 |
|
| 2007 |
Pankratz N. A two-stage classification approach identifies seven susceptibility genes for a simulated complex disease. Bmc Proceedings. 1: 1-6. PMID 18466528 DOI: 10.1186/1753-6561-1-S1-S30 |
0.413 |
|
| 2007 |
Pankratz ND, Foroud T. Genetics of Parkinson disease. Genetics in Medicine. 9: 801-811. PMID 18091429 DOI: 10.1097/Gim.0B013E31815Bf97C |
0.553 |
|
| 2007 |
Bickeböller H, Goddard KA, Igo RP, Kraft P, Lozano JP, Pankratz N, Balavarca Y, Bardel C, Charoen P, Croiseau P, Guo CY, Joo J, Köhler K, Madsen A, Malzahn D, et al. Issues in association mapping with high-density SNP data and diverse family structures. Genetic Epidemiology. 31: S22-33. PMID 18046763 DOI: 10.1002/Gepi.20277 |
0.418 |
|
| 2007 |
Nichols WC, Elsaesser VE, Pankratz N, Pauciulo MW, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T. LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8 Neurology. 69: 1737-1744. PMID 17804834 DOI: 10.1212/01.Wnl.0000278115.50741.4E |
0.56 |
|
| 2007 |
Nichols WC, Marek DK, Pauciulo MW, Pankratz N, Halter CA, Rudolph A, Shults CW, Wojcieszek J, Foroud T, Shults C, Marshall F, Oakes D, Shinaman A, Marder K, Conneally PM, et al. R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation Movement Disorders. 22: 254-257. PMID 17149721 DOI: 10.1002/Mds.21233 |
0.569 |
|
| 2006 |
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T, Nichols WC, Shults C, Marshall F, Oakes D, Shinaman A, Marder K, Conneally PM, et al. Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease Movement Disorders. 21: 2257-2260. PMID 17078063 DOI: 10.1002/Mds.21162 |
0.532 |
|
| 2006 |
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Shults CW, Foroud T, Nichols WC. Mutations in DJ-1 are rare in familial Parkinson disease Neuroscience Letters. 408: 209-213. PMID 16997464 DOI: 10.1016/J.Neulet.2006.09.003 |
0.578 |
|
| 2006 |
Foroud T, Pankratz N, Martinez M. Chromosome 5 and Parkinson disease. European Journal of Human Genetics. 14: 1106-1110. PMID 16736031 DOI: 10.1038/Sj.Ejhg.5201666 |
0.569 |
|
| 2006 |
Garringer HJ, Pankratz ND, Nichols WC, Reed T. Hearing impairment susceptibility in elderly men and the DFNA18 locus. Archives of Otolaryngology--Head & Neck Surgery. 132: 506-10. PMID 16702566 DOI: 10.1001/Archotol.132.5.506 |
0.335 |
|
| 2006 |
Pankratz N, Byder L, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC. Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 45-9. PMID 16116614 DOI: 10.1002/Mds.20663 |
0.578 |
|
| 2005 |
Pankratz N, Edenberg E, Foroud T. Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease Bmc Genetics. 6: 1-5. PMID 16451602 DOI: 10.1186/1471-2156-6-S1-S142 |
0.544 |
|
| 2005 |
Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. A mutation in myotilin causes spheroid body myopathy. Neurology. 65: 1936-40. PMID 16380616 DOI: 10.1212/01.Wnl.0000188872.28149.9A |
0.467 |
|
| 2005 |
Broderick JP, Sauerbeck LR, Foroud T, Huston J, Pankratz N, Meissner I, Brown RD. The Familial Intracranial Aneurysm (FIA) study protocol Bmc Medical Genetics. 6: 17-17. PMID 15854227 DOI: 10.1186/1471-2350-6-17 |
0.431 |
|
| 2005 |
Nichols WC, Pankratz N, Hernandez D, Paisán-Ruíz C, Jain S, Halter CA, Michaels VE, Reed T, Rudolph A, Shults CW, Singleton A, Foroud T. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet (London, England). 365: 410-2. PMID 15680455 DOI: 10.1016/S0140-6736(05)17828-3 |
0.551 |
|
| 2004 |
Pankratz N, Foroud T. Genetics of Parkinson disease. Neurorx. 1: 235-242. PMID 15717024 DOI: 10.1602/Neurorx.1.2.235 |
0.596 |
|
| 2004 |
Nichols WC, Uniacke SK, Pankratz N, Reed T, Simon DK, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 649-55. PMID 15197702 DOI: 10.1002/Mds.20097 |
0.59 |
|
| 2004 |
Pankratz N, Uniacke SK, Halter CA, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC. Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci. Neurology. 62: 1616-8. PMID 15136695 DOI: 10.1212/01.Wnl.0000123112.51368.10 |
0.588 |
|
| 2003 |
Pankratz N, Mukhopadhyay N, Huang S, Foroud T, Kirkwood SC. Identification of genes for complex disease using longitudinal phenotypes. Bmc Genetics. 4: S58. PMID 14975126 DOI: 10.1186/1471-2156-4-S1-S58 |
0.508 |
|
| 2003 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. Human Molecular Genetics. 12: 2599-608. PMID 12925570 DOI: 10.1093/Hmg/Ddg270 |
0.581 |
|
| 2003 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Significant linkage of Parkinson disease to chromosome 2q36-37. American Journal of Human Genetics. 72: 1053-7. PMID 12638082 DOI: 10.1086/374383 |
0.545 |
|
| 2003 |
Foroud T, Uniacke SK, Liu L, Pankratz N, Rudolph A, Halter C, Shults C, Marder K, Conneally PM, Nichols WC. Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. Neurology. 60: 796-801. PMID 12629236 DOI: 10.1212/01.Wnl.0000049470.00180.07 |
0.571 |
|
| 2002 |
Nichols WC, Pankratz N, Uniacke SK, Pauciulo MW, Halter C, Rudolph A, Conneally PM, Foroud T. Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families. Journal of Medical Genetics. 39: 489-92. PMID 12114481 DOI: 10.1136/Jmg.39.7.489 |
0.525 |
|
| 2002 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. American Journal of Human Genetics. 71: 124-35. PMID 12058349 DOI: 10.1086/341282 |
0.588 |
|
| 2001 |
Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Use of variable marker density, principal components, and neural networks in the dissection of disease etiology Genetic Epidemiology. 21: S732-737. PMID 11793770 DOI: 10.1002/Gepi.2001.21.S1.S732 |
0.516 |
|
| 2001 |
McClintick J, Koller DL, Pankratz N, Kirkwood SC, Naughton B, Foroud T. Parametric linkage analysis and disequilibrium methods to identify loci for complex disease Genetic Epidemiology. 21: S528-S533. PMID 11793731 DOI: 10.1002/Gepi.2001.21.S1.S528 |
0.556 |
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