Genetic signatures of exceptional longevity in humans
Sebastiani, Paola, Solovieff, Nadia, Dewan, Andrew T, Walsh, Kyle M, Puca, Annibale, Hartley, Stephen W, Melista, Efthymia, Andersen, Stacy, Dworkis, Daniel A, Wilk, Jemma B, Myers, Richard H, Steinberg, Martin H, Montano, Monty, Baldwin, Clinton T, Hoh, Josephine, Perls, Thomas T
Published in PloS one (18.01.2012)
Published in PloS one (18.01.2012)
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Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia
Ramoni, Marco F, Sebastiani, Paola, Nolan, Vikki, Baldwin, Clinton T, Steinberg, Martin H
Published in Nature genetics (01.04.2005)
Published in Nature genetics (01.04.2005)
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A search for age-related macular degeneration risk variants in Alzheimer disease genes and pathways
Logue, Mark W, Schu, Matthew, Vardarajan, Badri N, Farrell, John, Lunetta, Kathryn L, Jun, Gyungah, Baldwin, Clinton T, DeAngelis, Margaret M, Farrer, Lindsay A
Published in Neurobiology of aging (01.06.2014)
Published in Neurobiology of aging (01.06.2014)
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Multiple loci influencing hippocampal degeneration identified by genome scan
Melville, Scott A., Buros, Jacqueline, Parrado, Antonio R., Vardarajan, Badri, Logue, Mark W., Shen, Li, Risacher, Shannon L., Kim, Sungeun, Jun, Gyungah, DeCarli, Charles, Lunetta, Kathryn L., Baldwin, Clinton T., Saykin, Andrew J., Farrer, Lindsay A.
Published in Annals of neurology (01.07.2012)
Published in Annals of neurology (01.07.2012)
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A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia
Milton, Jacqueline N, Sebastiani, Paola, Solovieff, Nadia, Hartley, Stephen W, Bhatnagar, Pallav, Arking, Dan E, Dworkis, Daniel A, Casella, James F, Barron-Casella, Emily, Bean, Christopher J, Hooper, W Craig, DeBaun, Michael R, Garrett, Melanie E, Soldano, Karen, Telen, Marilyn J, Ashley-Koch, Allison, Gladwin, Mark T, Baldwin, Clinton T, Steinberg, Martin H, Klings, Elizabeth S
Published in PloS one (27.04.2012)
Published in PloS one (27.04.2012)
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RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans
Sebastiani, Paola, Montano, Monty, Puca, Annibale, Solovieff, Nadia, Kojima, Toshio, Wang, Meng C, Melista, Efthymia, Meltzer, Micah, Fischer, Sylvia E J, Andersen, Stacy, Hartley, Stephen H, Sedgewick, Amanda, Arai, Yasumichi, Bergman, Aviv, Barzilai, Nir, Terry, Dellara F, Riva, Alberto, Anselmi, Chiara Viviani, Malovini, Alberto, Kitamoto, Aya, Sawabe, Motoji, Arai, Tomio, Gondo, Yasuyuki, Steinberg, Martin H, Hirose, Nobuyoshi, Atzmon, Gil, Ruvkun, Gary, Baldwin, Clinton T, Perls, Thomas T
Published in PloS one (14.12.2009)
Published in PloS one (14.12.2009)
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Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease
Bhatnagar, Pallav, Barron-Casella, Emily, Bean, Christopher J, Milton, Jacqueline N, Baldwin, Clinton T, Steinberg, Martin H, Debaun, Michael, Casella, James F, Arking, Dan E
Published in PloS one (13.09.2013)
Published in PloS one (13.09.2013)
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Journal Article
Identification of Novel Candidate Genes for Alzheimer's Disease by Autozygosity Mapping using Genome Wide SNP Data
Sherva, Richard, Baldwin, Clinton T., Inzelberg, Rivka, Vardarajan, Badri, Cupples, L. Adrienne, Lunetta, Kathryn, Bowirrat, Abdalla, Naj, Adam, Pericak-Vance, Margaret, Friedland, Robert P., Farrer, Lindsay A.
Published in Journal of Alzheimer's disease (01.01.2011)
Published in Journal of Alzheimer's disease (01.01.2011)
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Journal Article
Whole genome sequences of a male and female supercentenarian, ages greater than 114 years
Sebastiani, Paola, Riva, Alberto, Montano, Monty, Pham, Phillip, Torkamani, Ali, Scherba, Eugene, Benson, Gary, Milton, Jacqueline N, Baldwin, Clinton T, Andersen, Stacy, Schork, Nicholas J, Steinberg, Martin H, Perls, Thomas T
Published in Frontiers in genetics (2012)
Published in Frontiers in genetics (2012)
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Journal Article
Fetal hemoglobin in sickle cell anemia
Akinsheye, Idowu, Alsultan, Abdulrahman, Solovieff, Nadia, Ngo, Duyen, Baldwin, Clinton T., Sebastiani, Paola, Chui, David H.K., Steinberg, Martin H.
Published in Blood (07.07.2011)
Published in Blood (07.07.2011)
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Journal Article
Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study
Reiman, Eric M, Arboleda-Velasquez, Joseph F, Quiroz, Yakeel T, Huentelman, Matthew J, Beach, Thomas G, Caselli, Richard J, Chen, Yinghua, Su, Yi, Myers, Amanda J, Hardy, John, Paul Vonsattel, Jean, Younkin, Steven G, Bennett, David A, De Jager, Philip L, Larson, Eric B, Crane, Paul K, Keene, C Dirk, Kamboh, M Ilyas, Kofler, Julia K, Duque, Linda, Gilbert, John R, Gwirtsman, Harry E, Buxbaum, Joseph D, Dickson, Dennis W, Frosch, Matthew P, Ghetti, Bernardino F, Lunetta, Kathryn L, Wang, Li-San, Hyman, Bradley T, Kukull, Walter A, Foroud, Tatiana, Haines, Jonathan L, Mayeux, Richard P, Pericak-Vance, Margaret A, Schneider, Julie A, Trojanowski, John Q, Farrer, Lindsay A, Schellenberg, Gerard D, Beecham, Gary W, Montine, Thomas J, Jun, Gyungah R
Published in Nature communications (03.02.2020)
Published in Nature communications (03.02.2020)
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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
NAJ, Adam C, JUN, Gyungah, LARSON, Eric B, BIRD, Thomas D, BOEVE, Bradley F, GRAFF-RADFORD, Neill R, JAGER, Philip L.de, EVANS, Denis, SCHNEIDER, Julie A, CARRASQUILLO, Minerva M, ERTEKIN-TANER, Nilufer, YOUNKIN, Steven G, BEECHAM, Gary W, CRUCHAGA, Carlos, KAUWE, John S. K, NOWOTNY, Petra, KRAMER, Patricia, HARDY, John, HUENTELMAN, Matthew J, MYERS, Amanda J, BARMADA, Michael M, DEMIRCI, F. Yesim, BALDWIN, Clinton T, WANG, Li-San, GREEN, Robert C, ROGAEVA, Ekaterina, STGEORGE-HYSLOP, Peter, EARNOLD, Steven, BARBER, Robert, BEACH, Thomas, BIGIO, Eileen H, BOWEN, James D, BOXER, Adam, BURKE, James R, BADRI NARAYAN VARDARAJAN, CAIRNS, Nigel J, CARLSON, Chriss, MCARNEY, Regina, CARROLL, Stevenl, CCHUI, Helena, CLARK, David G, CORNEVEAUX, Jason, COTMAN, Carl W, CUMMINGS, Jeffrey L, DECARLI, Charles, BUROS, Jacqueline, DEKOSKY, Steven T, DIAZ-ARRASTIA, Ramon, DICK, Malcolm, DICKSON, Dennis W, ELLIS, William G, FABER, Kelley M, FALLON, Kenneth B, FARLOW, Martin R, FERRIS, Steven, FROSCH, Matthew P, GALLINS, Paul J, BUXBAUM, Joseph D, JARVIK, Gail P, CRANE, Paul K
Published in Nature genetics (01.05.2011)
Published in Nature genetics (01.05.2011)
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Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
WHITCOMB, David C, LARUSCH, Jessica, GUDA, Nalini M, ORLICHENKO, Lidiya, ALKAADE, Samer, AMANN, Stephen T, ANDERSON, Michelle A, BAILLIE, John, BANKS, Peter A, CONWELL, Darwin, COTE, Gregory A, COTTON, Peter B, KRASINSKAS, Alyssa M, DISARIO, James, FARRER, Lindsay A, FORSMARK, Chris E, JOHNSTONE, Marianne, GARDNER, Timothy B, GELRUD, Andres, GREENHALF, William, HAINES, Jonathan L, HARTMAN, Douglas J, HAWES, Robert A, KLEI, Lambertus, LAWRENCE, Christopher, LEWIS, Michele, MAYERLE, Julia, MAYEUX, Richard, MELHEM, Nadine M, MONEY, Mary E, MUNIRAJ, Thiruvengadam, PAPACHRISTOU, Georgios I, PERICAK-VANCE, Margaret A, ROMAGNUOLO, Joseph, SMITH, Jill P, SCHELLENBERG, Gerard D, SHERMAN, Stuart, SIMON, Peter, SINGH, Vijay P, SLIVKA, Adam, STOLZ, Donna, SUTTON, Robert, ULRICH WEISS, Frank, MEL WILCOX, C, ZARNESCU, Narcis Octavian, BRAND, Randall E, WISNIEWSKI, Stephen R, NEOPTOLEMOS, John P, LERCH, Markus M, TECTOR, Matt, SANDHU, Bimaljit S
Published in Nature genetics (01.12.2012)
Published in Nature genetics (01.12.2012)
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Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4,and the Risk of Late-Onset Alzheimer Disease in African Americans
Reitz, Christiane, Jun, Gyungah, Naj, Adam, Rajbhandary, Ruchita, Vardarajan, Badri Narayan, Wang, Li-San, Valladares, Otto, Lin, Chiao-Feng, Larson, Eric B, Graff-Radford, Neill R, Evans, Denis, De Jager, Philip L, Crane, Paul K, Buxbaum, Joseph D, Murrell, Jill R, Raj, Towfique, Ertekin-Taner, Nilufer, Logue, Mark, Baldwin, Clinton T, Green, Robert C, Barnes, Lisa L, Cantwell, Laura B, Fallin, M. Daniele, Go, Rodney C. P, Griffith, Patrick, Obisesan, Thomas O, Manly, Jennifer J, Lunetta, Kathryn L, Kamboh, M. Ilyas, Lopez, Oscar L, Bennett, David A, Hendrie, Hugh, Hall, Kathleen S, Goate, Alison M, Byrd, Goldie S, Kukull, Walter A, Foroud, Tatiana M, Haines, Jonathan L, Farrer, Lindsay A, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Mayeux, Richard
Published in JAMA : the journal of the American Medical Association (10.04.2013)
Published in JAMA : the journal of the American Medical Association (10.04.2013)
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Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study
Reitz, Christiane, Kunkle, Brian W, Park, Yo Son, Beecham, Gary W, Myers, Amanda J, Bird, Thomas D, Boeve, Bradley F, Baldwin, Clinton T, Jarvik, Gail P, Crane, Paul K, Barmada, M Michael, Demirci, F Yesim, Cruchaga, Carlos, Kramer, Patricia L, Hardy, John, Green, Robert C, Larson, Eric B, Buxbaum, Joseph D, Evans, Denis A, Schneider, Julie A, Kamboh, M Ilyas, Saykin, Andrew J, Reiman, Eric M, Bennett, David A, Morris, John C, Montine, Thomas J, Goate, Alison M, Blacker, Deborah, Hakonarson, Hakon, Kukull, Walter A, Foroud, Tatiana M, Martin, Eden R, Mayeux, Richard P, Schellenberg, Gerard D, Pericak-Vance, Margaret A, Albin, Roger L, Apostolova, Liana G, Barnes, Lisa L, Becker, James T, Bowen, James D, Boxer, Adam, Burke, James R, Cairns, Nigel J, Cantwell, Laura B, Carney, Regina M, Chui, Helena C, Corneveaux, Jason, Crocco, Elizabeth A, DeCarli, Charles, Dickson, Dennis W, Duara, Ranjan, Faber, Kelley M, Farlow, Martin R, Frosch, Matthew P, Ganguli, Mary, Gearing, Marla, Geschwind, Daniel H, Gilbert, John R, Head, Elizabeth, Honig, Lawrence S, Jicha, Gregory A, Jin, Lee-Way, Karydas, Anna, Kaye, Jeffrey A, Kramer, Joel H, Levey, Allan I, Lin, Chiao-Feng, Lyketsos, Constantine G, Martiniuk, Frank, Masliah, Eliezer, McCormick, Wayne C, McCurry, Susan M, McKee, Ann C, Miller, Carol A, Miller, Joshua W, Olichney, John M, Parisi, Joseph E, Paulson, Henry L, Peskind, Elaine, Petersen, Ronald C, Pierce, Aimee, Poon, Wayne W, Raj, Ashok, Ringman, John M, Roberson, Erik D, Rosenberg, Roger N, Sano, Mary, Spina, Salvatore, Stern, Robert A, Tanzi, Rudolph E, Thornton-Wells, Tricia A, Trojanowski, John Q, Troncoso, Juan C, Valladares, Otto, Van Eldik, Linda J, Vardarajan, Badri N, Wishnek, Sarah, Woltjer, Randall L, Wright, Clinton B, Yu, Chang-En
Published in JAMA neurology (01.11.2014)
Published in JAMA neurology (01.11.2014)
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The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
Inzelberg, Rivka, Meng, Yan, Petersen, Ronald C, Sorbi, Sandro, Baldwin, Clinton T, Lee, Joseph H, Mayeux, Richard, Cupples, L Adrienne, Cuenco, Karen T, Katayama, Taiichi, Wakutani, Yosuke, Der, Sandy D, Pinessi, Lorenzo, Cheng, Rong, Willnow, Thomas E, Kawarai, Toshitaka, Hasegawa, Hiroshi, Gu, Yongjun, Chen, Fusheng, Friedland, Robert P, Rainero, Innocenzo, Fraser, Paul E, Zou, Fanggeng, Bujo, Hideaki, Lunetta, Kathryn L, Andersen, Olav M, Green, Robert C, Pardossi-Piquard, Raphaelle, Shibata, Nobuto, Bruni, Amalia, Graff-Radford, Neill, Rogaeva, Ekaterina, St George-Hyslop, Peter, Bohm, Christopher, Schmitt-Ulms, Gerold, Dickson, Dennis, Farrer, Lindsay A, Hampe, Wolfgang, Song, You-Qiang, Younkin, Steven, Duara, Ranjan
Published in Nature genetics (01.02.2007)
Published in Nature genetics (01.02.2007)
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Genetic Loci Influencing Lung Function . A Genomewide Scan in the Framingham Study
JOOST, OSCAR, WILK, JEMMA B, ADRIENNE CUPPLES, L, HARMON, MICHAEL, SHEARMAN, AMANDA M, BALDWIN, CLINTON T, O'CONNOR, GEORGE T, MYERS, RICHARD H, GOTTLIEB, DANIEL J
Published in American journal of respiratory and critical care medicine (15.03.2002)
Published in American journal of respiratory and critical care medicine (15.03.2002)
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Journal Article
Genetic signatures of exceptional longevity in humans
Sebastiani, Paola, Solovieff, Nadia, Puca, Annibale, Hartley, Stephen W, Melista, Efthymia, Andersen, Stacy, Dworkis, Daniel A, Wilk, Jemma B, Myers, Richard H, Steinberg, Martin H, Montano, Monty, Baldwin, Clinton T, Perls, Thomas T
Published in Science (American Association for the Advancement of Science) (01.07.2010)
Published in Science (American Association for the Advancement of Science) (01.07.2010)
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An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
Baldwin, Clinton T, Hoth, Christopher F, Amos, Jean A, da-Silva, Elias O, Milunsky, Aubrey
Published in Nature (London) (13.02.1992)
Published in Nature (London) (13.02.1992)
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