Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations von Carrasquillo, Minerva M., Zlotogora, Joel, Barges, Saleh, Chakravarti, Aravinda

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Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease von Chakravarti, Aravinda, Carrasquillo, Minerva M, McCallion, Andrew S, Puffenberger, Erik G, Kashuk, Carl S, Nouri, Nassim

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High-throughput variation detection and genotyping using microarrays von Cutler, D J, Zwick, M E, Carrasquillo, M M, Yohn, C T, Tobin, K P, Kashuk, C, Mathews, D J, Shah, N A, Eichler, E E, Warrington, J A, Chakravarti, A

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Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes von Shaw, S H, Carrasquillo, M M, Kashuk, C, Puffenberger, E G, Chakravarti, A

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Genetic Studies of the Mouse Mutations mahogany and mahoganoid von Miller, K. A, Gunn, T. M, Carrasquillo, M. M, Lamoreux, M. L, Galbraith, D. B, Barsh, G. S

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Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids von Harte, P.J., Wu, W., Carrasquillo, M.M., Matera, A.G.

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of lon... von van der Lee, SJ, Conway, OJ, Jansen, I, Carrasquillo, MM, van den Akker, E, Hernández, I, van Eijk, KR, Chen, JA, Zettergren, A, Andlauer, TFM, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, JE, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, MJ, Blennow, K, Skoog, I, Friese, MA, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, CM, Indakoetxea, B, Collij, LE, Scherer, M, Morenas-Rodríguez, E, Ironside, JW, van Berckel, BNM, Alcolea, D, Wiendl, H, Strickland, SL, Pastor, P, Rodríguez Rodríguez, E, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementi, Netherlands Brain Bank (NBB), Boeve, BF, Petersen, RC, Ferman, TJ, van Gerpen, JA, Reinders, MJT, Uitti, RJ, Tárraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, MC, Boada, M, Zettl, UK, van Schoor, NM, Beekman, M, Allen, M, Masliah, E, de Munain, AL, Pantelyat, A, Wszolek, ZK, Ross, OA, Dickson, DW, Graff-Radford, NR, Knopman, D, Rademakers, R, Lemstra, AW, Pijnenburg, YAL, Scheltens, P, Chinnery, PF, Hemmer, B, Huisman, MA, Troncoso, J, Moreno, F, Nohr, EA, Sørensen, TIA, Sánchez-Juan, P, Posthuma, D, Clarimón, J, Christensen, K, Scholz, SW, Ruiz, A, Slagboom, E, van der Flier, WM, Holstege, H

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SSLPs to map genetic differences between the 129 inbred strains and closed-colony, random-bred CD-1 mice von Threadgill, D W, Matin, A, Yee, D, Carrasquillo, M M, Henry, K R, Rollins, K G, Nadeau, J H, Magnuson, T

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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity von van der Lee, SJ, Conway, OJ, Jansen, I, Carrasquillo, MM, van den Akker, E, Hernández, I, van Eijk, KR, Chen, JA, Zettergren, A, Andlauer, TFM, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, JE, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, MJ, Blennow, K, Skoog, I, Friese, MA, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, CM, Indakoetxea, B, Collij, LE, Scherer, M, Morenas-Rodríguez, E, Ironside, JW, van Berckel, BNM, Alcolea, D, Wiendl, H, Strickland, SL, Pastor, P, Rodríguez Rodríguez, E, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer, EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The Interna, IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementi, Netherlands Brain Bank (NBB), Boeve, BF, Petersen, RC, Ferman, TJ, van Gerpen, JA, Reinders, MJT, Uitti, RJ, Tárraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, MC, Boada, M, Zettl, UK, van Schoor, NM, Beekman, M, Allen, M, Masliah, E, de Munain, AL, Pantelyat, A, Wszolek, ZK, Ross, OA, Dickson, DW, Graff-Radford, NR, Knopman, D, Rademakers, R, Lemstra, AW, Pijnenburg, YAL, Scheltens, P, Chinnery, PF, Hemmer, B, Huisman, MA, Troncoso, J, Moreno, F, Nohr, EA, Sørensen, TIA, Sánchez-Juan, P, Posthuma, D, Clarimón, J, Christensen, K, Scholz, SW, Ruiz, A, Slagboom, E, van der Flier, WM, Holstege, H

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Polygenic risk and hazard scores for Alzheimer's disease prediction von Leonenko, G, Shoai, M, Frizzati, A, Bossu, P, Fox, NC, Williams, J, Tsolaki, M, Avramidou, D, Germanou, A, Love, S, McGuinness, B, Passmore, P, Warren, JD, Kawalia, A, Hughes, JT, Lupton, MK, Powell, J, Bonuccelli, U, Uphill, J, Fisher, E, Soininen, H, Bisceglio, G, Ma, L, Carrasquillo, MM, Daniilidou, M, Galimberti, D, Scarpini, E, Peters, O, Ramirez, A, Pichler, S, Riemenschneider, M, Heun, R, Kolsch, H, Heuser, I, Rujescu, D, Giegling, I, Hull, M, Lovestone, S, Cruchaga, C, Feulner, T, Holmes, C, Mann, D, Pickering-Brown, S, Livingston, G, Bass, NJ, Vronskaya, M, Morgan, T, Cushion, TD, Jones, L, Marshall, R, Grozeva, D, O'Donovan, MC, Owen, MJ, Russo, G, Maier, W, Jessen, F, Wichmann, H-E, Vellas, B, Vardy, E, Moebus, S, Dichgans, M, Klopp, N, Turton, J, Brown, K, Medway, C, Hoffmann, P, Daniele, A, Gallacher, J, van den Bussche, H, Brayne, C, Riedel-Heller, S, Powell, JF, Al-Chalabi, A, Pastor, P, Diez-Fairen, M, Lynch, A, Lawlor, B, Coto, E, Alvarez, V, Mead, S, Ryan, N, Nacmias, B, Rodriguez-Rodriguez, E, Sanchez-Juan, P, Shofany, J, Banaj, N, Sacchinelli, E, Smith, AD, Warden, D, Cupidi, C, Bruni, AC, Gallo, M, Harold, D, Cecchetti, R, Mecocci, P, Warner, N, Wilcock, G, Deloukas, P, Corcoran, C, Tschanz, J

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CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease von Ma, Y, Chung, J, Zhang, X, Kunkle, BW, Naj, AC, Bennett, DA, De Jager, PL, Mayeux, R, Haines, JL, Pericak-Vance, MA, Schellenberg, GD, Farrer, LA, Lunetta, KL, Albert, MS, Albin, RL, Apostolova, LG, Asthana, S, Baldwin, CT, Boeve, BF, Boxer, A, Burke, JR, Cairns, NJ, Cao, C, Carlson, CS, Carrasquillo, MM, Crane, P, Cribbs, DH, Crocco, EA, Cruchaga, C, DeCarli, C, Demirci, FY, De Jager, P, Dick, M, Dickson, D, Duara, R, Farlow, MR, Ferris, S, Foroud, TM, Frosch, M, Geschwind, DH, Goate, AM, Graff-Radford, NR, Growdon, JH, Hakonarson, H, Hamilton, RL, Harrell, LE, Head, E, Honig, LS, Jarvik, GP, Jicha, GA, Jin, L-W, Jun, G, Kamboh, MI, Kauwe, JSK, Kaye, JA, Kowall, NW, Kramer, JH, LaFerla, FM, Larson, E, Levey, AI, Li, G, Lieberman, AP, Lyketsos, CG, Mack, WJ, Martiniuk, F, Mash, D, Masliah, E, McCormick, WC, McCurry, SM, Miller, CA, Morris, JC, Murrell, JR, Myers, AJ, Olichney, JM, Parisi, JE, Paulson, HL, Perry, W, Peskind, E, Petersen, RC, Potter, H, Raskind, M, Reitz, C, Ringman, JM, Sano, M, Schneider, LS, Seeley, WW, Sonnen, JA, Hyslop, PSG, Tanzi, RE, Thornton-Wells, TA, Troncoso, JC, Tsuang, DW, Vonsattel, J-P, Weintraub, S, Welsh-Bohmer, KA, Wishnek, S, Woltjer, RL, Wright, CB, Yu, C-E, Yu, L

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A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression von Carrasquillo, MM, Allen, M, Burgess, JD, Wang, X, Strickland, SL, Aryal, S, Siuda, J, Kachadoorian, ML, Medway, C, Younkin, CS, Nair, A, Wang, C, Chanana, P, Serie, D, Nguyen, T, Lincoln, S, Malphrus, KG, Morgan, K, Golde, TE, Price, ND, White, CC, De Jager, PL, Bennett, DA, Asmann, YW, Crook, JE, Petersen, RC, Graff-Radford, NR, Dickson, DW, Younkin, SG, Ertekin-Taner, N

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Transethnic genome-wide scan identifies novel Alzheimer's disease loci von Jun, GR, Chung, J, Mez, J, Barber, R, Beecham, GW, Bennett, DA, Buxbaum, JD, Byrd, GS, Carrasquillo, MM, Crane, PK, Cruchaga, C, De Jager, P, Ertekin-Taner, N, Evans, D, Fallin, MD, Foroud, TM, Friedland, RP, Goate, AM, Graff-Radford, NR, Hendrie, H, Hall, KS, Hamilton-Nelson, KL, Inzelberg, R, Kamboh, MI, Kauwe, JSK, Kukull, WA, Kunkle, BW, Kuwano, R, Larson, EB, Logue, MW, Manly, JJ, Martin, ER, Montine, TJ, Mukherjee, S, Naj, A, Reiman, EM, Reitz, C, Sherva, R, St George-Hyslop, PH, Thornton, T, Younkin, SG, Vardarajan, BN, Wang, L-S, Wendlund, JR, Winslow, AR, Haines, J, Mayeux, R, Pericak-Vance, MA, Schellenberg, G, Lunetta, KL, Farrer, LA

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Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease von Schott, JM, Crutch, SJ, Carrasquillo, MM, Uphill, J, Shakespeare, TJ, Ryan, NS, Yong, KX, Lehmann, M, Ertekin-Taner, N, Graff-Radford, NR, Boeve, BF, Murray, ME, Khan, QU, Petersen, RC, Dickson, DW, Knopman, DS, Rabinovici, GD, Miller, BL, González, AS, Gil-Néciga, E, Snowden, JS, Harris, J, Pickering-Brown, SM, Louwersheimer, E, van der Flier, WM, Scheltens, P, Pijnenburg, YA, Galasko, D, Sarazin, M, Dubois, B, Magnin, E, Galimberti, D, Scarpini, E, Cappa, SF, Hodges, JR, Halliday, GM, Bartley, L, Carrillo, MC, Bras, JT, Hardy, J, Rossor, MN, Collinge, J, Fox, NC, Mead, S

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Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease von Bellenguez, C, Choi, SH, Holmans, P, DeStefano, AL, Lambert, JC, Naj, AC, Grenier-Boley, B, Russo, G, Ikram, MA, Zelenika, D, Kamatani, Y, Lin, CF, Schmidt, H, Vronskaya, M, United Kingdom Brain Expression Consortium, Johnson, AD, Bihoreau, MT, Reitz, C, Hollingworth, P, Hanon, O, Buxbaum, JD, Campion, D, Baldwin, C, Cruchaga, C, Craig, D, Amin, N, Berr, C, Lopez, OL, De Jager, PL, Deramecourt, V, Evans, D, Eiriksdottir, G, Sleegers, K, Fiévet, N, Huentelman, MJ, Gill, M, Keller, L, Barberger-Gateau, P, Dufouil, C, Gallacher, J, George-Hyslop, PS, Clarimon, J, Yu, L, Tsolaki, M, Bossù, P, Spalletta, G, Sorbi, S, Garcia, FS, Fox, NC, Naranjo, MC, Brayne, C, Mancuso, M, Moebus, S, Mecocci, P, Pilotto, A, Frank-García, A, Panza, F, Solfrizzi, V, Caffarra, P, Nacmias, B, Perry, W, Mayhaus, M, Lannfelt, L, Pichler, S, Carrasquillo, MM, Beekly, D, Younkin, SG, Hamilton-Nelson, KL, Gu, W, Pastor, P, Owen, MJ, Jonsson, PV, Soininen, H, Blacker, D, Bennett, DA, Holmes, C, Rotter, JI, Brice, A, Foroud, TM, Hannequin, D, Nalls, MA, Ritchie, K, Kauwe, JS, Boerwinkle, E, Riemenschneider, M, Hiltunen, M, Schmidt, R, Rujescu, D, Mayeux, R, Nöthen, MM, Graff, C, Haines, JL, Pericak-Vance, MA, Van Broeckhoven, C, Farrer, LA, Ramirez, A, Seshadri, S, Schellenberg, GD, Amouyel, P, Williams, J

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Correction: genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease von Jones, L, Holmans, PA, Hamshere, ML, Harold, D, Moskvina, V, Ivanov, D, Pocklington, A, Abraham, R, Hollingworth, P, Sims, R, Gerrish, A, Pahwa, JS, Jones, N, Stretton, A, Morgan, AR, Lovestone, S, Powell, J, Proitsi, P, Lupton, MK, Brayne, C, Rubinsztein, DC, Gill, M, Lawlor, B, Lynch, A, Morgan, K, Brown, KS, Passmore, PA, Craig, D, McGuinness, B, Todd, S, Holmes, C, Mann, D, Smith, AD, Love, S, Kehoe, PG, Mead, S, Fox, N, Rossor, M, Collinge, J, Maier, W, Jessen, F, Schürmann, B, van den Bussche, H, Heuser, I, Peters, O, Kornhuber, J, Wiltfang, J, Dichgans, M, Frölich, L, Hampel, H, Hüll, M, Rujescu, D, Goate, AM, Kauwe, JS, Cruchaga, C, Nowotny, P, Morris, JC, Mayo, K, Livingston, G, Bass, NJ, Gurling, H, McQuillin, A, Gwilliam, R, Deloukas, P, Al-Chalabi, A, Shaw, CE, Singleton, AB, Guerreiro, R, Mühleisen, TW, Nöthen, MM, Moebus, S, Jöckel, KH, Klopp, N, Wichmann, HE, Rüther, E, Carrasquillo, MM, Pankratz, VS, Younkin, SG, Hardy, J, O'Donovan, MC, Owen, MJ, Williams, J

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Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease von Jones, L, Holmans, PA, Hamshere, ML, Harold, D, Moskvina, V, Ivanov, D, Pocklington, A, Abraham, R, Hollingworth, P, Sims, R, Gerrish, A, Pahwa, JS, Jones, N, Stretton, A, Morgan, AR, Lovestone, S, Powell, J, Proitsi, P, Lupton, MK, Brayne, C, Rubinsztein, DC, Gill, M, Lawlor, B, Lynch, A, Morgan, K, Brown, KS, Passmore, PA, Craig, D, McGuinness, B, Todd, S, Holmes, C, Mann, D, Smith, AD, Love, S, Kehoe, PG, Mead, S, Fox, N, Rossor, M, Collinge, J, Maier, W, Jessen, F, Schurmann, B, van den Bussche, H, Heuser, I, Peters, O, Kornhuber, J, Wiltfang, J, Dichgans, M, Frolich, L, Hampel, H, Hull, M, Rujescu, D, Goate, AM, Kauwe, JSK, Cruchaga, C, Nowotny, P, Morris, JC, Mayo, K, Livingston, G, Bass, NJ, Gurling, H, McQuillin, A, Gwilliam, R, Deloukas, P, Al-Chalabi, A, Shaw, CE, Singleton, AB, Guerreiro, R, Muhleisen, TW, Nothen, MM, Moebus, S, Jockel, KH, Klopp, N, Wichmann, HE, Ruther, E, Carrasquillo, MM, Pankratz, VS, Younkin, SG, Hardy, J, O'Donovan, MC, Owen, MJ, Williams, J

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Pattern and frequency reconfigurable annular slot antenna using PIN diodes von Symeon Nikolaou, Bairavasubramanian, R., Lugo, C., Carrasquillo, I., Thompson, D.C., Ponchak, G.E., Papapolymerou, J., Tentzeris, M.M.

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