Works by Cannon-Albright, Lisa

Results: 105
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    Breast Cancer Is Increased in Women With Primary Ovarian Insufficiency Open Access.

    Published in:
    Journal of Clinical Endocrinology & Metabolism, 2025, v. 110, n. 5, p. e1678, doi. 10.1210/clinem/dgae480
    By:
    • Allen-Brady, Kristina;
    • Moore, Barry;
    • Verrilli, Lauren E;
    • Alvord, Margaret A;
    • Kern, Marina;
    • Camp, Nicola;
    • Kelley, Kristen;
    • Letourneau, Joseph;
    • Cannon-Albright, Lisa;
    • Yandell, Mark;
    • Johnstone, Erica B;
    • Welt, Corrine K
    Publication type:
    Article
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    gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.

    Published in:
    Genetic Epidemiology, 2017, v. 41, n. 4, p. 297, doi. 10.1002/gepi.22036
    By:
    • Larson, Nicholas B.;
    • McDonnell, Shannon;
    • Cannon Albright, Lisa;
    • Teerlink, Craig;
    • Stanford, Janet;
    • Ostrander, Elaine A.;
    • Isaacs, William B.;
    • Xu, Jianfeng;
    • Cooney, Kathleen A.;
    • Lange, Ethan;
    • Schleutker, Johanna;
    • Carpten, John D.;
    • Powell, Isaac;
    • Bailey‐Wilson, Joan E.;
    • Cussenot, Olivier;
    • Cancel‐Tassin, Geraldine;
    • Giles, Graham G.;
    • MacInnis, Robert J.;
    • Maier, Christiane;
    • Whittemore, Alice S.
    Publication type:
    Article
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    Allelic Association in Large Pedigrees.

    Published in:
    Genetic Epidemiology, 2001, v. 21, p. S571, doi. 10.1002/gepi.2001.21.s1.s571
    By:
    • Gutin, Alexander;
    • Abkevich, Victor;
    • Camp, Nicola J.;
    • Farnham, James M.;
    • Cannon-Albright, Lisa;
    • Thomas, Alun
    Publication type:
    Article
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    Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States.

    Published in:
    JAMA Neurology, 2015, v. 72, n. 2, p. 209, doi. 10.1001/jamaneurol.2014.2157
    By:
    • Li-San Wang;
    • Naj, Adam C.;
    • Graham, Robert R.;
    • Crane, Paul K.;
    • Kunkle, Brian W.;
    • Cruchaga, Carlos;
    • Murcia, Josue D. Gonzalez;
    • Cannon-Albright, Lisa;
    • Baldwin, Clinton T.;
    • Zetterberg, Henrik;
    • Blennow, Kaj;
    • Kukull, Walter A.;
    • Faber, Kelley M.;
    • Schupf, Nicole;
    • Norton, Maria C.;
    • Tschanz, JoAnn T.;
    • Munger, Ronald G.;
    • Corcoran, Christopher D.;
    • Rogaeva, Ekaterina;
    • Chiao-Feng Lin
    Publication type:
    Article
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    Risk modifiers in carriers of brca1 mutations.

    Published in:
    International Journal of Cancer, 1995, v. 64, n. 6, p. 394, doi. 10.1002/ijc.2910640608
    By:
    • Narod, Steven A.;
    • Goldgar, David;
    • Cannon-Albright, Lisa;
    • Weber, Barbara;
    • Moslehi, Roxanna;
    • Ives, Elizabeth;
    • Lenoir, Gilbert;
    • Lynch, Henry
    Publication type:
    Article
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    A likely HOXC4 predisposition variant for Chiari malformations.

    Published in:
    Journal of Neurosurgery, 2023, v. 139, n. 1, p. 266, doi. 10.3171/2022.10.jns22956
    By:
    • Brockmeyer, Douglas L.;
    • Cheshier, Samuel H.;
    • Stevens, Jeff;
    • Facelli, Julio C.;
    • Rowe, Kerry;
    • Heiss, John D.;
    • Musolf, Anthony;
    • Viskochil, David H.;
    • Allen-Brady, Kristina L.;
    • Cannon-Albright, Lisa A.
    Publication type:
    Article
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    Genome-wide association study identifies three new melanoma susceptibility loci.

    Published in:
    Nature Genetics, 2011, v. 43, n. 11, p. 1108, doi. 10.1038/ng.959
    By:
    • Barrett, Jennifer H;
    • Iles, Mark M;
    • Harland, Mark;
    • Taylor, John C;
    • Aitken, Joanne F;
    • Andresen, Per Arne;
    • Akslen, Lars A;
    • Armstrong, Bruce K;
    • Avril, Marie-Francoise;
    • Azizi, Esther;
    • Bakker, Bert;
    • Bergman, Wilma;
    • Bianchi-Scarrà, Giovanna;
    • Bressac-de Paillerets, Brigitte;
    • Calista, Donato;
    • Cannon-Albright, Lisa A;
    • Corda, Eve;
    • Cust, Anne E;
    • D?bniak, Tadeusz;
    • Duffy, David
    Publication type:
    Article
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    Genome-wide association study identifies three loci associated with melanoma risk.

    Published in:
    Nature Genetics, 2009, v. 41, n. 8, p. 920, doi. 10.1038/ng.411
    By:
    • Bishop, D. Timothy;
    • Demenais, Florence;
    • Iles, Mark M.;
    • Harland, Mark;
    • Taylor, John C.;
    • Corda, Eve;
    • Randerson-Moor, Juliette;
    • Aitken, Joanne F.;
    • Avril, Marie-Francoise;
    • Azizi, Esther;
    • Bakker, Bert;
    • Bianchi-Scarrà, Giovanna;
    • Paillerets, Brigitte Bressac-de;
    • Calista, Donato;
    • Cannon-Albright, Lisa A.;
    • Chin-A-Woeng, Thomas;
    • Dębniak, Tadeusz;
    • Galore-Haskel, Gilli;
    • Ghiorzo, Paola;
    • Gut, Ivo
    Publication type:
    Article
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    Legal terms of use and public genealogy websites.

    Published in:
    Journal of Law & the Biosciences, 2020, v. 7, n. 1, p. 1, doi. 10.1093/jlb/lsaa063
    By:
    • Contreras, Jorge L;
    • Schultz, Kyle;
    • Teerlink, Craig C;
    • Maness, Tim;
    • Meyer, Laurence J;
    • Cannon-Albright, Lisa A
    Publication type:
    Article
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    A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma.

    Published in:
    2018
    By:
    • Teerlink, Craig C;
    • Huff, Chad;
    • Stevens, Jeff;
    • Yu, Yao;
    • Holmen, Sheri L;
    • Silvis, Mark R;
    • Trombetti, Kirby;
    • Zhao, Hua;
    • Grossman, Douglas;
    • Farnham, James M;
    • Wen, Jingran;
    • Facelli, Julio C;
    • Thomas, Alun;
    • Babst, Markus;
    • Florell, Scott R;
    • Meyer, Laurence;
    • Zone, John J;
    • Leachman, Sancy;
    • Cannon-Albright, Lisa A
    Publication type:
    journal article
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    Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 24, p. 5490, doi. 10.1093/hmg/ddw349
    By:
    • Luedeke, Manuel;
    • Rinckleb, Antje E.;
    • FitzGerald, Liesel M.;
    • Geybels, Milan S.;
    • Schleutker, Johanna;
    • Eeles, Rosalind A.;
    • Teixeira, Manuel R.;
    • Cannon-Albright, Lisa;
    • Ostrander, Elaine A.;
    • Weikert, Steffen;
    • Herkommer, Kathleen;
    • Wahlfors, Tiina;
    • Visakorpi, Tapio;
    • Leinonen, Katri A.;
    • Tammela, Teuvo L. J.;
    • Cooper, Colin S.;
    • Kote-Jarai, Zsofia;
    • Edwards, Sandra;
    • Goh, Chee L.;
    • McCarthy, Frank
    Publication type:
    Article
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    Analysis of high‐risk pedigrees identifies 11 candidate variants for Alzheimer's disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 2, p. 307, doi. 10.1002/alz.12397
    By:
    • Teerlink, Craig C.;
    • Miller, Justin B.;
    • Vance, Elizabeth L.;
    • Staley, Lyndsay A.;
    • Stevens, Jeffrey;
    • Tavana, Justina P.;
    • Cloward, Matthew E.;
    • Page, Madeline L.;
    • Dayton, Louisa;
    • Cannon‐Albright, Lisa A.;
    • Kauwe, John S.K.
    Publication type:
    Article
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    O3‐13‐01: HIGHLY PENETRANT LATE‐ONSET ALZHEIMER DISEASE VARIANTS IN NOTCH3 IN ASHKENAZI JEWS.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P918, doi. 10.1016/j.jalz.2019.06.4696
    By:
    • Patel, Devanshi;
    • Mez, Jesse;
    • Vardarajan, Badri N.;
    • Staley, Lyndsay;
    • Chung, Jaeyoon;
    • Zhang, Xiaoling;
    • Farrell, John;
    • Rynkiewicz, Michael J.;
    • Cannon-Albright, Lisa;
    • Teerlink, Craig;
    • Stevens, Jeffrey;
    • Corcoran, Christopher;
    • Gonzalez Murcia, Josue D.;
    • Lopez, Oscar L.;
    • Mayeux, Richard;
    • Haines, Jonathan L.;
    • Pericak-Vance, Margaret A.;
    • Schellenberg, Gerard D.;
    • Kauwe, John;
    • Lunetta, Kathryn L.
    Publication type:
    Article
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    LINKAGE AND WHOLE GENOME SEQUENCE ANALYSIS OF ALZHEIMER'S DISEASE RESILIENCE AND RISK.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P675, doi. 10.1016/j.jalz.2016.06.1325
    By:
    • Kauwe, Keoni;
    • Arano, Ivan;
    • Bras, Jose T.;
    • Cannon-Albright, Lisa;
    • Cruchaga, Carlos;
    • Goate, Alison M.;
    • Gonzalez Murcia, Josue D.;
    • Guerreiro, Rita;
    • Hardy, John;
    • Hsu, Simon;
    • Karch, Celeste;
    • Munger, Ronald G.;
    • Norton, Maria C.;
    • Ridge, Perry G.;
    • Sassi, Celeste;
    • Singleton, Andrew;
    • Teerlink, Craig;
    • Tschanz, JoAnn;
    • Younkin, Steven G.;
    • Corcoran, Christopher
    Publication type:
    Article
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    Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 11, p. 1271
    By:
    • Camp, Nicola J.;
    • Cannon-Albright, Lisa A.;
    • Farnham, James M.;
    • Baffoe-Bonnie, Agnes B.;
    • George, Asha;
    • Powell, Isaac;
    • Bailey-Wilson, Joan E.;
    • Carpten, John D.;
    • Giles, Graham G.;
    • Hopper, John L.;
    • Severi, Gianluca;
    • English, Dallas R.;
    • Foulkes, William D.;
    • Maehle, Lovise;
    • Moller, Pal;
    • Eeles, Ros;
    • Easton, Douglas;
    • Badzioch, Michael D.;
    • Whittemore, Alice S.;
    • Oakley-Girvan, Ingrid
    Publication type:
    Article
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