Works matching AU Scott, William K.

Results: 120
    1
    2

    Life After the Screen: Making Sense of Many P-Values.

    Published in:
    Genetic Epidemiology, 2001, v. 21, p. S546, doi. 10.1002/gepi.2001.21.s1.s546
    By:
    • Schmidt, Silke;
    • Shao, Yujun;
    • Hauser, Elizabeth R.;
    • Slifer, Susan H.;
    • Martin, Eden R.;
    • Scott, William K.;
    • Speer, Marcy C.;
    • Pericak-Vance, Margaret A.
    Publication type:
    Article
    3
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    Overall Diet Quality and Age-Related Macular Degeneration.

    Published in:
    Ophthalmic Epidemiology, 2010, v. 17, n. 1, p. 58, doi. 10.3109/09286580903450353
    By:
    • Montgomery, Martha P.;
    • Kamel, Freya;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.;
    • Postel, Eric A.;
    • Agarwal, Anita;
    • Richards, Marie;
    • Scott, William K.;
    • Schmidt, Silke
    Publication type:
    Article
    6
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    Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.

    Published in:
    2001
    By:
    • Martin, Eden R.;
    • Scott, William K.;
    • Nance, Martha A.;
    • Watts, Ray L.;
    • Hubble, Jean P.;
    • Koller, William C.;
    • Lyons, Kelly;
    • Patwa, Rajesh;
    • Stern, Matthew B.;
    • Colcher, Amy;
    • Hiner, Bradley C.;
    • Jankovic, Joseph;
    • Ondo, William G.;
    • Allen, Jr., Fred H.;
    • Goetz, Christopher G.;
    • Small, Gary W.;
    • Masterman, Donna;
    • Mastaglia, Frank;
    • Laing, Nigel G.;
    • Stajich, Jeffrey M.
    Publication type:
    journal article
    8

    Complete Genomic Screen in Parkinson Disease.

    Published in:
    JAMA: Journal of the American Medical Association, 2001, v. 286, n. 18, p. 2239, doi. 10.1001/jama.286.18.2239
    By:
    • Scott, William K.;
    • Nance, Martha A.;
    • Watts, Ray L.;
    • Hubble, Jean P.;
    • Koller, William C.;
    • Lyons, Kelly;
    • Pahwa, Rajesh;
    • Stern, Matthew B.;
    • Colcher, Amy;
    • Hiner, Bradley C.;
    • Jankovic, Joseph;
    • Ondo, William G.;
    • Allen, Fred H.;
    • Goetz, Christopher G.;
    • Small, Gary W.;
    • Masterman, Donna;
    • Mastaglia, Frank;
    • Laing, Nigel G.;
    • Stajich, Jeffrey M.;
    • Slotterbeck, Brandon
    Publication type:
    Article
    9

    Examination of MGMT as a risk gene for dementia in the Amish.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 1, p. 1, doi. 10.1002/alz.14356
    By:
    • Main, Leighanne R.;
    • Song, Yeunjoo E.;
    • Lynn, Audrey;
    • Laux, Renee A.;
    • Miskimen, Kristy L.;
    • Osterman, Michael D.;
    • Cuccaro, Michael L.;
    • Ogrocki, Paula K.;
    • Lerner, Alan J.;
    • Vance, Jeffery M.;
    • Fuzzell, M. Denise;
    • Fuzzell, Sarada L.;
    • Hochstetler, Sherri D.;
    • Dorfsman, Daniel A.;
    • Caywood, Laura J.;
    • Prough, Michael B.;
    • Adams, Larry D.;
    • Clouse, Jason E.;
    • Herington, Sharlene D.;
    • Scott, William K.
    Publication type:
    Article
    10

    Harnessing chromatin loops to identify susceptibility genes in different populations for Alzheimer's disease: rs3851179 links to PICALM not EED.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.092337
    By:
    • Wang, Liyong;
    • Xu, Wanying;
    • Rajabli, Farid;
    • Celis, Katrina;
    • Lu, Leina;
    • Gearing, Marla;
    • Bennett, David A.;
    • Flanagan, Margaret E;
    • Weintraub, Sandra;
    • Geula, Changiz;
    • Schuck, Theresa;
    • Scott, William K.;
    • Dykxhoorn, Derek M.;
    • Griswold, Anthony J.;
    • Pericak‐Vance, Margaret A.;
    • Young, Juan I;
    • Jin, Fulai;
    • Vance, Jeffery M.
    Publication type:
    Article
    11

    Local ancestry in Apoe3: Friend or Foe?

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.091750
    By:
    • Moura, Sofia;
    • Celis, Katrina;
    • Nasciben, Luciana Bertholim;
    • Rajabli, Farid;
    • Rivero, Joe;
    • Hamilton‐Nelson, Kara L.;
    • Whitehead, Patrice L.;
    • Gearing, Marla;
    • Bennett, David A.;
    • Flanagan, Margaret E;
    • Weintraub, Sandra;
    • Geula, Changiz;
    • Scott, William K.;
    • Davis, David A.;
    • Vontell, Regina T;
    • Schuck, Theresa;
    • Dykxhoorn, Derek M.;
    • Pericak‐Vance, Margaret A.;
    • Griswold, Anthony J.;
    • Young, Juan I
    Publication type:
    Article
    12

    African origin haplotype protective for AD in APOEe4 carriers: exploring potential mechanisms.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.091487
    By:
    • Nasciben, Luciana Bertholim;
    • Nuytemans, Karen;
    • Vasquez, Marina Lipkin;
    • Rajabli, Farid;
    • Young, Juan I;
    • Dykxhoorn, Derek M.;
    • Wang, Liyong;
    • Scott, William K.;
    • Davis, David A.;
    • Vontell, Regina T;
    • Pericak‐Vance, Margaret A;
    • Griswold, Anthony J.;
    • Vance, Jeffery M.
    Publication type:
    Article
    13

    Do Alzheimer Disease genetic loci influence the risk of Age‐Related Macular Degeneration?

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.089652
    By:
    • Moore, Noel C.;
    • Song, Yeunjoo E.;
    • Lynn, Audrey;
    • Miskimen, Kristy L.;
    • Wang, Weihuan;
    • Laux, Renee A.;
    • Fuzzell, Sarada L.;
    • Hochstetler, Sherri D.;
    • Caywood, Laura J.;
    • Clouse, Jason E.;
    • Herington, Sharlene D.;
    • Nittala, Muneeswar Gupta;
    • Sadda, SriniVas R;
    • Stambolian, Dwight;
    • Lerner, Alan J.;
    • Vance, Jeffery M.;
    • Cuccaro, Michael L.;
    • Scott, William K.;
    • Pericak‐Vance, Margaret A.;
    • Haines, Jonathan L.
    Publication type:
    Article
    14

    Genetic analysis of cognitive preservation in the midwestern Amish reveals a novel locus on chromosome 2.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 11, p. 7453, doi. 10.1002/alz.14045
    By:
    • Main, Leighanne R.;
    • Song, Yeunjoo E.;
    • Lynn, Audrey;
    • Laux, Renee A.;
    • Miskimen, Kristy L.;
    • Osterman, Michael D.;
    • Cuccaro, Michael L.;
    • Ogrocki, Paula K.;
    • Lerner, Alan J.;
    • Vance, Jeffery M.;
    • Fuzzell, Denise;
    • Fuzzell, Sarada L.;
    • Hochstetler, Sherri D.;
    • Dorfsman, Daniel A.;
    • Caywood, Laura J.;
    • Prough, Michael B.;
    • Adams, Larry D.;
    • Clouse, Jason E.;
    • Herington, Sharlene D.;
    • Scott, William K.
    Publication type:
    Article
    15
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    Whole exome sequencing of extreme age-related macular degeneration phenotypes.

    Published in:
    Molecular Vision, 2016, v. 22, p. 1
    By:
    • Sardell, Rebecca J.;
    • Cooke Bailey, Jessica N.;
    • Courtenay, Monique D.;
    • Whitehead, Patrice;
    • Laux, Reneé A.;
    • Adams, Larry D.;
    • Fortun, Jorge A.;
    • Brantley Jr., Milam A.;
    • Kovach, Jaclyn L.;
    • Schwartz, Stephen G.;
    • Agarwal, Anita;
    • Scott, William K.;
    • Haines, Jonathan L.;
    • Pericak-Vance, Margaret A.
    Publication type:
    Article
    17

    Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 10, p. 1, doi. 10.1371/journal.pgen.1007667
    By:
    • Scott, William K.;
    • Medie, Felix Mba;
    • Ruffin, Felicia;
    • Sharma-Kuinkel, Batu K.;
    • Cyr, Derek D.;
    • Guo, Shengru;
    • Dykxhoorn, Derek M.;
    • Skov, Robert L.;
    • Bruun, Niels E.;
    • Dahl, Anders;
    • Lerche, Christian J.;
    • Petersen, Andreas;
    • Larsen, Anders Rhod;
    • Lauridsen, Trine Kiilerich;
    • Johansen, Helle Krogh;
    • Ullum, Henrik;
    • Sørensen, Erik;
    • Hassager, Christian;
    • Bundgaard, Henning;
    • Schønheyder, Henrik C.
    Publication type:
    Article
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    The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.

    Published in:
    Movement Disorders, 2015, v. 30, n. 2, p. 278, doi. 10.1002/mds.26065
    By:
    • Sharp, Madeleine E.;
    • Caccappolo, Elise;
    • Mejia‐Santana, Helen;
    • Tang, Ming‐X.;
    • Rosado, Llency;
    • Orbe Reilly, Martha;
    • Ruiz, Diana;
    • Louis, Elan D.;
    • Comella, Cynthia;
    • Nance, Martha;
    • Bressman, Susan;
    • Scott, William K.;
    • Tanner, Caroline;
    • Waters, Cheryl;
    • Fahn, Stanley;
    • Cote, Lucien;
    • Ford, Blair;
    • Rezak, Michael;
    • Novak, Kevin;
    • Friedman, Joseph H.
    Publication type:
    Article
    21

    Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease.

    Published in:
    Movement Disorders, 2014, v. 29, n. 6, p. 827, doi. 10.1002/mds.25838
    By:
    • Nuytemans, Karen;
    • Inchausti, Vanessa;
    • Beecham, Gary W.;
    • Wang, Liyong;
    • Dickson, Dennis W.;
    • Trojanowski, John Q.;
    • Lee, Virginia M.‐Y.;
    • Mash, Deborah C.;
    • Frosch, Matthew P.;
    • Foroud, Tatiana M.;
    • Honig, Lawrence S.;
    • Montine, Thomas J.;
    • Dawson, Ted M.;
    • Martin, Eden R.;
    • Scott, William K.;
    • Vance, Jeffery M.
    Publication type:
    Article
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    Cognitive and Motor Function in Long-Duration PARKIN-Associated Parkinson Disease.

    Published in:
    JAMA Neurology, 2014, v. 71, n. 1, p. 62, doi. 10.1001/jamaneurol.2013.4498
    By:
    • Alcalay, Roy N.;
    • Caccappolo, Elise;
    • Mejia-Santana, Helen;
    • Ming Xin Tang;
    • Rosado, Llency;
    • Reilly, Martha Orbe;
    • Ruiz, Diana;
    • Louis, Elan D.;
    • Comella, Cynthia L.;
    • Nance, Martha A.;
    • Bressman, Susan B.;
    • Scott, William K.;
    • Tanner, Caroline M.;
    • Mickel, Susan H.;
    • Waters, Cheryl H.;
    • Fahn, Stanley;
    • Cote, Lucien J.;
    • Frucht, Steven J.;
    • Ford, Blair;
    • Rezak, Michael
    Publication type:
    Article
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    C90RF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease.

    Published in:
    Annals of Human Genetics, 2013, v. 77, n. 5, p. 351, doi. 10.1111/ahg.12033
    By:
    • Nuytemans, Karen;
    • Bademci, Güney;
    • Kohli, Martin M.;
    • Beecham, Gary W.;
    • Wang, Liyong;
    • Young, Juan I.;
    • Nahab, Fatta;
    • Martin, Eden R.;
    • Gilbert, John R.;
    • Benatar, Michael;
    • Haines, Jonathan L.;
    • Scott, William K.;
    • Züchner, Stephan;
    • Pericak‐Vance, Margaret A.;
    • Vance, Jeffery M.
    Publication type:
    Article
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    Genome-Wide Association and Linkage Study in the Amish Detects a Novel Candidate Late-Onset Alzheimer Disease Gene.

    Published in:
    Annals of Human Genetics, 2012, v. 76, n. 5, p. 342, doi. 10.1111/j.1469-1809.2012.00721.x
    By:
    • Cummings, Anna C.;
    • Jiang, Lan;
    • Velez Edwards, Digna R.;
    • McCauley, Jacob L.;
    • Laux, Renee;
    • McFarland, Lynne L.;
    • Fuzzell, Denise;
    • Knebusch, Clare;
    • Caywood, Laura;
    • Reinhart-Mercer, Lori;
    • Nations, Laura;
    • Gilbert, John R.;
    • Konidari, Ioanna;
    • Tramontana, Michael;
    • Cuccaro, Michael L.;
    • Scott, William K.;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.
    Publication type:
    Article
    30

    Successful Aging Shows Linkage to Chromosomes 6, 7, and 14 in the Amish.

    Published in:
    Annals of Human Genetics, 2011, v. 75, n. 4, p. 516, doi. 10.1111/j.1469-1809.2011.00658.x
    By:
    • Edwards, Digna R. Velez;
    • Gilbert, John R.;
    • Jiang, Lan;
    • Gallins, Paul J.;
    • Caywood, Laura;
    • Creason, Marilyn;
    • Fuzzell, Denise;
    • Knebusch, Clare;
    • Jackson, Charles E.;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.;
    • Scott, William K.
    Publication type:
    Article
    31

    A Genome-Wide Linkage Screen in the Amish with Parkinson Disease Points to Chromosome 6.

    Published in:
    Annals of Human Genetics, 2011, v. 75, n. 3, p. 351, doi. 10.1111/j.1469-1809.2011.00643.x
    By:
    • Cummings, Anna C.;
    • Lee, Stephen L.;
    • McCauley, Jacob L.;
    • Jiang, Lan;
    • Crunk, Amy;
    • McFarland, Lynne L.;
    • Gallins, Paul J.;
    • Fuzzell, Denise;
    • Knebusch, Clare;
    • Jackson, Charles E.;
    • Scott, William K.;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.
    Publication type:
    Article
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    Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease.

    Published in:
    Annals of Human Genetics, 2010, v. 74, n. 2, p. 97, doi. 10.1111/j.1469-1809.2009.00560.x
    By:
    • Edwards, Todd L.;
    • Scott, William K.;
    • Almonte, Cherylyn;
    • Burt, Amber;
    • Powell, Eric H.;
    • Beecham, Gary W.;
    • Wang, Liyong;
    • Züchner, Stephan;
    • Konidari, Ioanna;
    • Wang, Gaofeng;
    • Singer, Carlos;
    • Nahab, Fatta;
    • Scott, Burton;
    • Stajich, Jeffrey M.;
    • Pericak-Vance, Margaret;
    • Haines, Jonathan;
    • Vance, Jeffery M.;
    • Martin, Eden R.
    Publication type:
    Article
    35

    Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

    Published in:
    Nature Genetics, 2010, v. 42, n. 9, p. 781, doi. 10.1038/ng.642
    By:
    • Hamza, Taye H.;
    • Zabetian, Cyrus P.;
    • Tenesa, Albert;
    • Laederach, Alain;
    • Montimurro, Jennifer;
    • Yearout, Dora;
    • Kay, Denise M.;
    • Doheny, Kimberly F.;
    • Paschall, Justin;
    • Pugh, Elizabeth;
    • Kusel, Victoria I.;
    • Collura, Randall;
    • Roberts, John;
    • Griffith, Alida;
    • Samii, Ali;
    • Scott, William K.;
    • Nutt, John;
    • Factor, Stewart A.;
    • Payami, Haydeh
    Publication type:
    Article
    36

    An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.

    Published in:
    Nature Genetics, 1999, v. 22, n. 1, p. 19, doi. 10.1038/8729
    By:
    • Rogaeva, Ekaterina A.;
    • Premkumar, Smita;
    • Grubber, Janet;
    • Serneels, Lutgarde;
    • Scott, William K.;
    • Kawarai, Toshitaka;
    • Song, Youqiang;
    • Hill, De'Lisa M.;
    • Abou-Donia, Suzanne M.;
    • Martin, Eden R.;
    • Vance, Jeffrey J.;
    • Yu, Gang;
    • Orlacchio, Antonio;
    • Pei, York;
    • Nishimura, Masaki;
    • Supala, Agres;
    • Roberge, Brenda;
    • Saunders, Ann M.;
    • Roses, Allen D.
    Publication type:
    Article
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    Role of autophagy genetic variants for the risk of Candida infections.

    Published in:
    Medical Mycology, 2014, v. 52, n. 4, p. 333, doi. 10.1093/mmy/myt035
    By:
    • Rosentul, Diana C.;
    • Plantinga, Theo S.;
    • Farcas, Marius;
    • Oosting, Marije;
    • Hamza, Omar J. M.;
    • Scott, William K.;
    • Alexander, Barbara D.;
    • Yang, John C.;
    • Laird, Gregory M.;
    • Joosten, Leo A. B.;
    • van der Meer, Jos W. M.;
    • Perfect, John R.;
    • Kullberg, Bart-Jan;
    • van der Ven, Andre J. A. M.;
    • Johnson, Melissa D.;
    • Netea, Mihai G.
    Publication type:
    Article
    41

    Human genetic susceptibility to Candida infections.

    Published in:
    Medical Mycology, 2012, v. 50, n. 8, p. 785, doi. 10.3109/13693786.2012.690902
    By:
    • Plantinga, Theo S.;
    • Johnson, Melissa D.;
    • Scott, William K.;
    • Joosten, Leo A.B.;
    • van der Meer, Jos W. M.;
    • Perfect, John R.;
    • Kullberg, Bart Jan;
    • Netea, Mihai G.
    Publication type:
    Article
    42

    C3 R102G polymorphism increases risk of age-related macular degeneration.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 12, p. 1821, doi. 10.1093/hmg/ddn075
    By:
    • Spencer, Kylee L.;
    • Olson, Lana M.;
    • Anderson, Brent M.;
    • Schnetz-Boutaud, Nathalie;
    • Scott, William K.;
    • Gallins, Paul;
    • Agarwal, Anita;
    • Postel, Eric A.;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.
    Publication type:
    Article
    43

    Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 7, p. 971, doi. 10.1093/hmg/ddm369
    By:
    • Spencer, Kylee L.;
    • Hauser, Michael A.;
    • Olson, Lana M.;
    • Schmidt, Silke;
    • Scott, William K.;
    • Gallins, Paul;
    • Agarwal, Anita;
    • Postel, Eric A.;
    • Pericak-Vance, Margaret A.;
    • Haines, Jonathan L.
    Publication type:
    Article
    44
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    Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.

    Published in:
    Human Molecular Genetics, 2004, v. 13, n. 5, p. 573, doi. 10.1093/hmg/ddh059
    By:
    • Li, Yi-Ju;
    • Oliveira, Sofia A.;
    • Xu, Puting;
    • Martin, Eden R.;
    • Stenger, Judith E.;
    • Hulette, Christine;
    • Scherzer, Clemens R.;
    • Hauser, Michael A.;
    • Scott, William K.;
    • Small, Gary W.;
    • Nance, Martha A.;
    • Watts, Ray L.;
    • Hubble, Jean P.;
    • Koller, William C.;
    • Pahwa, Rajesh;
    • Stern, Matthew B.;
    • Hiner, Bradley C.;
    • Jankovic, Joseph;
    • Goetz, Christopher G.;
    • Mastaglia, Frank
    Publication type:
    Article
    46

    Glutathione S-transferase omega-1 modifiesage-at-onset of Alzheimer disease and Parkinson disease.

    Published in:
    Human Molecular Genetics, 2003, v. 12, n. 24, p. 3259, doi. 10.1093/hmg/ddg357
    By:
    • Li, Yi-Ju;
    • Oliveira, Sofia A.;
    • Xu, Puting;
    • Martin, Eden R.;
    • Stenger, Judith E.;
    • Scherzer, Clemens R.;
    • Hauser, Michael A.;
    • Scott, William K.;
    • Small, Gary W.;
    • Nance, Martha A.;
    • Watts, Ray L.;
    • Hubble, Jean P.;
    • Koller, William C.;
    • Pahwa, Rajesh;
    • Stern, Mathew B.;
    • Hiner, Bradley C.;
    • Jankovic, Joseph;
    • Goetz, Christopher G.;
    • Mastaglia, Frank;
    • Middleton, Lefkos T.
    Publication type:
    Article
    47

    Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans.

    Published in:
    PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0179033
    By:
    • Yan, Qin;
    • Ahn, Sun Hee;
    • Medie, Felix Mba;
    • Sharma-Kuinkel, Batu K.;
    • Park, Lawrence P.;
    • Scott, William K.;
    • Deshmukh, Hitesh;
    • Tsalik, Ephraim L.;
    • Cyr, Derek D.;
    • Woods, Christopher W.;
    • Yu, Chen-Hsin Albert;
    • Adams, Carlton;
    • Qi, Robert;
    • Hansen, Brenda;
    • JrFowler, Vance G.
    Publication type:
    Article
    48
    49

    Reply.

    Published in:
    Annals of Neurology, 2003, v. 54, n. 3, p. 416
    By:
    • Sofia A. Oliveira;
    • William K. Scott;
    • Eden R. Martin;
    • Margaret A. Pericak-Vance;
    • Jeffery M. Vance
    Publication type:
    Article
    50

    Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.

    Published in:
    Annals of Neurology, 2003, v. 53, n. 5, p. 624
    By:
    • Sofia A. Oliveira;
    • William K. Scott;
    • Eden R. Martin;
    • Martha A. Nance;
    • Ray L. Watts;
    • Jean P. Hubble;
    • William C. Koller;
    • Rajesh Pahwa;
    • Matthew B. Stern;
    • Bradley C. Hiner;
    • William G. Ondo;
    • Fred H. Allen;
    • Burton L. Scott;
    • Christopher G. Goetz;
    • Gary W. Small;
    • Frank Mastaglia;
    • Jeffrey M. Stajich;
    • Fengyu Zhang;
    • Michael W. Booze;
    • Michelle P. Winn
    Publication type:
    Article