A two-stage classification approach identifies seven susceptibility genes for a simulated complex disease

por Pankratz, Nathan
Publicado 2007

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

por Pankratz, Nathan D
Publicado 2009

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

por Pankratz, Nathan, Edenberg, Ellen, Foroud, Tatiana
Publicado 2005

Identification of genes for complex disease using longitudinal phenotypes

por Pankratz, Nathan, Mukhopadhyay, Nitai, Huang, Shuguang, Foroud, Tatiana, Kirkwood, Sandra Close
Publicado 2003

Lower Expression of CFTR Is Associated with Higher Mortality in a Meta-Analysis of Individuals with Colorectal Cancer

por Scott, Patricia, Wang, Shuo, Onyeaghala, Guillaume, Pankratz, Nathan, Starr, Timothy, Prizment, Anna E.
Publicado 2023

Exome sequencing findings in children with annular pancreas

por Pitsava, Georgia, Pankratz, Nathan, Lane, John, Yang, Wei, Rigler, Shannon, Shaw, Gary M., Mills, James L.
Publicado 2023

The Familial Intracranial Aneurysm (FIA) study protocol

por Broderick, Joseph P, Sauerbeck, Laura R, Foroud, Tatiana, Huston, John, Pankratz, Nathan, Meissner, Irene, Brown, Robert D
Publicado 2005

Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number

por Pillalamarri, Vamsee, Shi, Wen, Say, Conrad, Yang, Stephanie, Lane, John, Guallar, Eliseo, Pankratz, Nathan, Arking, Dan E.
Publicado 2022

Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores

por Folsom, Aaron R., Tang, Weihong, Hong, Ching-Ping, Rosamond, Wayne D., Lane, John A., Cushman, Mary, Pankratz, Nathan
Publicado 2023

Long-Term Air Pollution Exposure and Mitochondrial DNA Copy Number: An Analysis of UK Biobank Data

por Hong, Yun Soo, Battle, Stephanie L., Puiu, Daniela, Shi, Wen, Pankratz, Nathan, Zhao, Di, Arking, Dan E., Guallar, Eliseo
Publicado 2023

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

por Onyeaghala, Guillaume, Lane, John, Pankratz, Nathan, Nelson, Heather H., Thyagarajan, Bharat, Walcheck, Bruce, Anderson, Kristin E., Prizment, Anna E.
Publicado 2019

Prostate Cancer Mortality Associated with Aggregate Polymorphisms in Androgen-Regulating Genes: The Atherosclerosis Risk in the Communities (ARIC) Study

por Prizment, Anna E., McSweeney, Sean, Pankratz, Nathan, Joshu, Corinne E., Hwang, Justin H., Platz, Elizabeth A., Ryan, Charles J.
Publicado 2021

Genome Sequencing of Consanguineous Family Implicates Ubiquitin-Specific Protease 53 (USP53) Variant in Psychosis/Schizophrenia: Wild-Type Expression in Murine Hippocampal CA 1–3 a...

por Kanwal, Ambreen, Sheikh, Sohail A., Aslam, Faiza, Yaseen, Samina, Beetham, Zachary, Pankratz, Nathan, Clabots, Connie R., Naz, Sadaf, Pardo, José V.
Publicado 2023

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

por Ryder, Justin R., Pankratz, Nathan D., Dengel, Donald R., Pankow, James S., Jacobs, David R., Sinaiko, Alan R., Gooty, Vasu, Steinberger, Julia
Publicado 2017

OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort

por Hernández-Ramírez, Laura, Chasseloup, Fanny, Faucz, Fabio, Lodish, Maya, Pankratz, Nathan, Chittiboina, Prashant, Lane, John, Kay, Denise, Mills, James, Stratakis, Constantine
Publicado 2019

OR06-01 The Role of Germline Defects in Cushing’s Disease

por Hernández-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Faucz, Fabio R, Chittiboina, Prashant, Denise, Kay M, Mills, James L, Stratakis, Constantine A
Publicado 2020

RF01 | PMON167 Isolated Cushing's Disease Associated With Rare Germline SDHx Variants

por Chittiboina, Prashant, Kay, Denise M, Mills, James L, Stratakis, Constantine A, Hernãndez-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Faucz, Fabio R
Publicado 2022

THU214 Exploratory Study Of The Association Of Genetic Factors With Recovery Of Hypothalamic-Pituitary-Adrenal Axis In Cushing Disease

por Nguyen, Matthew H, Zhang, Wei, Pankratz, Nathan, Lane, John, Chittiboina, Prashant, Faucz, Fabio R, Liu, Aiyi, Mills, James L, Stratakis, Constantine A, Tatsi, Christina
Publicado 2023

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

por Simon, David K, Pankratz, Nathan, Kissell, Diane K, Pauciulo, Michael W, Halter, Cheryl A, Rudolph, Alice, Pfeiffer, Ronald F, Nichols, William C, Foroud, Tatiana
Publicado 2010

Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization study

por Weng, Lu-Chen, Roetker, Nicholas S., Lutsey, Pamela L., Alonso, Alvaro, Guan, Weihua, Pankow, James S., Folsom, Aaron R., Steffen, Lyn M., Pankratz, Nathan, Tang, Weihong
Publicado 2018