Ngā hua rapu - Pankratz, Nathan

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  1. 1
    A two-stage classification approach identifies seven susceptibility genes for a simulated complex disease

    A two-stage classification approach identifies seven susceptibility genes for a simulated complex disease mā Pankratz, Nathan

    I whakaputaina 2007
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  2. 2
    Non-redundant summary scores applied to the North American Rheumatoid Arthritis Consortium dataset

    Non-redundant summary scores applied to the North American Rheumatoid Arthritis Consortium dataset mā Pankratz, Nathan D

    I whakaputaina 2009
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  3. 3
    Genetics of Parkinson Disease

    Genetics of Parkinson Disease mā Pankratz, Nathan, Foroud, Tatiana

    I whakaputaina 2004
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  4. 4
    Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

    Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease mā Pankratz, Nathan, Edenberg, Ellen, Foroud, Tatiana

    I whakaputaina 2005
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  5. 5
    Genetic and nongenetic risk factors for childhood cancer

    Genetic and nongenetic risk factors for childhood cancer mā Spector, Logan G., Pankratz, Nathan, Marcotte, Erin L.

    I whakaputaina 2014
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  6. 6
    Identification of genes for complex disease using longitudinal phenotypes

    Identification of genes for complex disease using longitudinal phenotypes mā Pankratz, Nathan, Mukhopadhyay, Nitai, Huang, Shuguang, Foroud, Tatiana, Kirkwood, Sandra Close

    I whakaputaina 2003
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  7. 7
    Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans

    Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans mā Folsom, Aaron R., Roetker, Nicholas S., Kelley, Spencer T., Tang, Weihong, Pankratz, Nathan

    I whakaputaina 2017
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  8. 8
    Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association

    Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association mā Kirkpatrick, Robert M., McGue, Matt, Iacono, William G., Miller, Michael B., Basu, Saonli, Pankratz, Nathan

    I whakaputaina 2013
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  9. 9
    The Familial Intracranial Aneurysm (FIA) study protocol

    The Familial Intracranial Aneurysm (FIA) study protocol mā Broderick, Joseph P, Sauerbeck, Laura R, Foroud, Tatiana, Huston, John, Pankratz, Nathan, Meissner, Irene, Brown, Robert D

    I whakaputaina 2005
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  10. 10
    Clinical Correlates of Depressive Symptoms in Familial Parkinson's Disease

    Clinical Correlates of Depressive Symptoms in Familial Parkinson's Disease mā Pankratz, Nathan, Marder, Karen S., Halter, Cheryl A., Rudolph, Alice, Shults, Cliff W., Nichols, William C., Foroud, Tatiana

    I whakaputaina 2008
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  11. 11
    Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The Atherosclerosis Risk in Communities (ARIC) Study

    Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The Atherosclerosis Risk in Communities (ARIC) Study mā Pankow, James S., Tang, Weihong, Pankratz, Nathan, Guan, Weihua, Weng, Lu-Chen, Cushman, Mary, Boerwinkle, Eric, Folsom, Aaron R.

    I whakaputaina 2017
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  12. 12
    Significant Linkage of Parkinson Disease to Chromosome 2q36-37

    Significant Linkage of Parkinson Disease to Chromosome 2q36-37 mā Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana

    I whakaputaina 2003
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  13. 13
    Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations

    Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations mā Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana

    I whakaputaina 2002
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  14. 14
    Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study

    Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study mā Onyeaghala, Guillaume, Lane, John, Pankratz, Nathan, Nelson, Heather H., Thyagarajan, Bharat, Walcheck, Bruce, Anderson, Kristin E., Prizment, Anna E.

    I whakaputaina 2019
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  15. 15
    Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study

    Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study mā Tang, Weihong, Stimson, Mary Rachel, Basu, Saonli, Heckbert, Susan R., Cushman, Mary, Pankow, James S., Folsom, Aaron R., Pankratz, Nathan

    I whakaputaina 2019
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  16. 16
    Factors Related to Fungiform Papillae Density: The Beaver Dam Offspring Study

    Factors Related to Fungiform Papillae Density: The Beaver Dam Offspring Study mā Fischer, Mary E., Cruickshanks, Karen J., Schubert, Carla R., Pinto, Alex, Klein, Ronald, Pankratz, Nathan, Pankow, James S., Huang, Guan-Hua

    I whakaputaina 2013
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  17. 17
    Prostate Cancer Mortality Associated with Aggregate Polymorphisms in Androgen-Regulating Genes: The Atherosclerosis Risk in the Communities (ARIC) Study

    Prostate Cancer Mortality Associated with Aggregate Polymorphisms in Androgen-Regulating Genes: The Atherosclerosis Risk in the Communities (ARIC) Study mā Prizment, Anna E., McSweeney, Sean, Pankratz, Nathan, Joshu, Corinne E., Hwang, Justin H., Platz, Elizabeth A., Ryan, Charles J.

    I whakaputaina 2021
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  18. 18
    Odor Identification and Cognitive Function in the Beaver Dam Offspring Study

    Odor Identification and Cognitive Function in the Beaver Dam Offspring Study mā Schubert, Carla R., Cruickshanks, Karen J., Fischer, Mary E., Huang, Guan-Hua, Klein, Ronald, Pankratz, Nathan, Zhong, Wenjun, Nondahl, David M.

    I whakaputaina 2013
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  19. 19
    Heritability of Vascular Structure and Function: A Parent–Child Study

    Heritability of Vascular Structure and Function: A Parent–Child Study mā Ryder, Justin R., Pankratz, Nathan D., Dengel, Donald R., Pankow, James S., Jacobs, David R., Sinaiko, Alan R., Gooty, Vasu, Steinberger, Julia

    I whakaputaina 2017
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  20. 20
    OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort

    OR24-6 Non-syndromic Cushing's Disease Due To CDKN1B Mutations: Novel Mutations And Phenotypic Features In A Large Pediatric Cohort mā Hernández-Ramírez, Laura, Chasseloup, Fanny, Faucz, Fabio, Lodish, Maya, Pankratz, Nathan, Chittiboina, Prashant, Lane, John, Kay, Denise, Mills, James, Stratakis, Constantine

    I whakaputaina 2019
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