Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders von Truong, D. T., Shriberg, L. D., Smith, S. D., Chapman, K. L., Scheer-Cohen, A. R., DeMille, M. M. C., Adams, A. K., Nato, A. Q., Wijsman, E. M., Eicher, J. D., Gruen, J. R.

Volltext

Divergent Haplotypes and Human History as Revealed in a Worldwide Survey of X-Linked DNA Sequence Variation von Shimada, Makoto K., Panchapakesan, Karuna, Tishkoff, Sarah A., Nato, Alejandro Q., Hey, Jody

Volltext

Human whole-exome genotype data for Alzheimer’s disease von Leung, Yuk Yee, Naj, Adam C., Chou, Yi-Fan, Valladares, Otto, Schmidt, Michael, Hamilton-Nelson, Kara, Wheeler, Nicholas, Lin, Honghuang, Gangadharan, Prabhakaran, Qu, Liming, Clark, Kaylyn, Kuzma, Amanda B., Lee, Wan-Ping, Cantwell, Laura, Nicaretta, Heather, Haines, Jonathan, Farrer, Lindsay, Seshadri, Sudha, Brkanac, Zoran, Cruchaga, Carlos, Pericak-Vance, Margaret, Mayeux, Richard P., Bush, William S., Destefano, Anita, Martin, Eden, Schellenberg, Gerard D., Wang, Li-San

Volltext

Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees von Ullah, Ehsan, Mall, Raghvendra, Abbas, Mostafa M, Kunji, Khalid, Nato, Jr, Alejandro Q, Bensmail, Halima, Wijsman, Ellen M, Saad, Mohamad

Volltext

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech von Peter, Beate, Wijsman, Ellen M, Nato, Jr, Alejandro Q, Matsushita, Mark M, Chapman, Kathy L, Stanaway, Ian B, Wolff, John, Oda, Kaori, Gabo, Virginia B, Raskind, Wendy H

Volltext

GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data von Kunji, Khalid, Ullah, Ehsan, Nato, Alejandro Q, Wijsman, Ellen M, Saad, Mohamad

Volltext

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes von Chapman, Nicola H., Nato, Alejandro Q., Bernier, Raphael, Ankenman, Katy, Sohi, Harkirat, Munson, Jeff, Patowary, Ashok, Archer, Marilyn, Blue, Elizabeth M., Webb, Sara Jane, Coon, Hilary, Raskind, Wendy H., Brkanac, Zoran, Wijsman, Ellen M.

Volltext

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project von Naj, Adam C., Lin, Honghuang, Vardarajan, Badri N., White, Simon, Lancour, Daniel, Ma, Yiyi, Schmidt, Michael, Sun, Fangui, Butkiewicz, Mariusz, Bush, William S., Kunkle, Brian W., Malamon, John, Amin, Najaf, Choi, Seung Hoan, Hamilton-Nelson, Kara L., van der Lee, Sven J., Gupta, Namrata, Koboldt, Daniel C., Saad, Mohamad, Wang, Bowen, Nato, Alejandro Q., Sohi, Harkirat K., Kuzma, Amanda, Wang, Li-San, Cupples, L. Adrienne, van Duijn, Cornelia, Seshadri, Sudha, Schellenberg, Gerard D., Boerwinkle, Eric, Bis, Joshua C., Dupuis, Josée, Salerno, William J., Wijsman, Ellen M., Martin, Eden R., DeStefano, Anita L.

Volltext

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation von Li, Bo I., Matteson, Paul G., Ababon, Myka F., Nato, Alejandro Q., Lin, Yong, Nanda, Vikas, Matise, Tara C., Millonig, James H.

Volltext

Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations von Horimoto, Andrea R.V.R., Boyken, Lisa A., Blue, Elizabeth E., Grinde, Kelsey E., Nafikov, Rafael A., Sohi, Harkirat K., Nato, Alejandro Q., Bis, Joshua C., Brusco, Luis I., Morelli, Laura, Ramirez, Alfredo, Dalmasso, Maria Carolina, Temple, Seth, Satizabal, Claudia, Browning, Sharon R., Seshadri, Sudha, Wijsman, Ellen M., Thornton, Timothy A.

Volltext

PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers von Nato, Jr, Alejandro Q, Chapman, Nicola H, Sohi, Harkirat K, Nguyen, Hiep D, Brkanac, Zoran, Wijsman, Ellen M

Volltext

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer’s Disease Sequencing Project von Blue, Elizabeth E., Bis, Joshua C., Dorschner, Michael O., Tsuang, Debby W., Barral, Sandra M., Beecham, Gary, Below, Jennifer E., Bush, William S., Butkiewicz, Mariusz, Cruchaga, Carlos, DeStefano, Anita, Farrer, Lindsay A., Goate, Alison, Haines, Jonathan, Jaworski, Jim, Jun, Gyungah, Kunkle, Brian, Kuzma, Amanda, Lee, Jenny J., Lunetta, Kathryn L., Ma, Yiyi, Martin, Eden, Naj, Adam, Nato, Alejandro Q., Navas, Patrick, Nguyen, Hiep, Reitz, Christiane, Reyes, Dolly, Salerno, William, Schellenberg, Gerard D., Seshadri, Sudha, Sohi, Harkirat, Thornton, Timothy A., Valadares, Otto, van Duijn, Cornelia, Vardarajan, Badri N., Wang, Li-San, Boerwinkle, Eric, Dupuis, Josée, Pericak-Vance, Margaret A., Mayeux, Richard, Wijsman, Ellen M.

Volltext

Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP von Nafikov, Rafael A., Nato, Alejandro Q., Sohi, Harkirat, Wang, Bowen, Brown, Lisa, Horimoto, Andrea R., Vardarajan, Badri N., Barral, Sandra M., Tosto, Giuseppe, Mayeux, Richard P., Thornton, Timothy A., Blue, Elizabeth, Wijsman, Ellen M.

Volltext

Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four U.S. populations: The Population Architecture using Genom... von Zhang, Lili, Buzkova, Petra, Wassel, Christina L, Roman, Mary J, North, Kari E, Crawford, Dana C, Boston, Jonathan, Brown-Gentry, Kristin D, Cole, Shelley A, Deelman, Ewa, Goodloe, Robert, Wilson, Sarah, Heiss, Gerardo, Jenny, Nancy S, Jorgensen, Neal W, Matise, Tara C, McClellan, Bob E, Nato, Alejandro Q, Ritchie, Marylyn D, Franceschini, Nora, Kao, W.H. Linda

Volltext

A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease von Zhang, Xiaoling, Ma, Yiyi, Lancour, Daniel, Farrell, John J., Chung, Jaeyoon, Dinh, Huyen, Doddapeneni, Harsha, English, Adam, Gibbs, Richard A., Han, Yi, Jayaseelan, Joy, Kalra, Divya, Khan, Ziad, Lee, Sandra, Liu, Yue, Muzny, Donna, Nasser, Waleed, White, Simon, Worley, Kim, Zhu, Yiming, Beiser, Alexa, Chen, Yuning, Chung, Jaeyoon, Cupples, L. Adrienne, DeStefano, Anita, Dupuis, Josee, Farrell, John, Farrer, Lindsay, Lancour, Daniel, Lin, Honghuang, Sarnowski, Chloe, Zhang, Xiaoling, Choi, Seung Hoan, Gabriel, Stacey, Butkiewicz, Mariusz, Haines, Jonathan, Song, Yeunjoo, Barral, Sandra, Reitz, Christiane, Reyes, Dolly, Tosto, Giuseppe, Vardarajan, Badri, Amad, Shahzad, Amin, Najaf, Ikram, M. Afran, van Duijn, Cornelia, Vanderspek, Ashley, Schmidt, Helena, Goate, Alison, Marcora, Edoardo, Foroud, Tatiana, Feolo, Michael, Launer, Lenore J., Bennett, David A., Xia, Li Charlie, Beecham, Gary, Hamilton-Nelson, Kara, Jaworski, James, Martin, Eden, Pericak-Vance, Margaret, Rajabli, Farid, Schmidt, Michael, Cantwell, Laura, Childress, Micah, Chou, Yi-Fan, Cweibel, Rebecca, Leung, Yuk Yee, Lin, Han-Jen, Malamon, John, Naj, Adam, Valladares, Otto, Wang, Li-San, Wang, Weixin, Zhang, Nancy, Boerwinkle, Eric, Bressler, Jan, Fornage, Myriam, Jian, Xueqiu, Liu, Xiaoming, Blue, Elizabeth, Brown, Lisa, Day, Tyler, Dorschner, Michael, Horimoto, Andrea R., Nato, Alejandro Q., Navas, Pat, Nguyen, Hiep, Rice, Kenneth, Sohi, Harkirat, Thornton, Timothy, Tsuang, Debby, Cruchaga, Carlos, Fulton, Robert S., Koboldt, Daniel C., Larson, David E., Waligorski, Jason, Wilson, Richard K., Haines, Jonathan L., Pericak-Vance, Margaret A., Lunetta, Kathryn L.

Volltext

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities von Musolf, Anthony, Nato, Jr, Alejandro Q, Londono, Douglas, Zhou, Lisheng, Matise, Tara C, Gordon, Derek

Volltext

GENOMEWIDE LINKAGE ANALYSIS IDENTIFIES NOVEL CANDIDATE GENES FOR ALZHEIMER’S DISEASE von Ahmad, Shahzad, Amin, Najaf, Blue, Elizabeth, van der Lee, Sven J, Nato, Alejandro Q, Sohi, Harkirat, Wang, Bowen, Boerwinkle, Eric, DeStefano, Anita L, Wijsman, Ellen, van Duijn, Cornelia M

Volltext

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data von Saad, Mohamad, Nato, Jr, Alejandro Q, Grimson, Fiona L, Lewis, Steven M, Brown, Lisa A, Blue, Elizabeth M, Thornton, Timothy A, Thompson, Elizabeth A, Wijsman, Ellen M

Volltext

Comparison and Assessment of Family- and Population-Based Genotype Imputation Methods in Large Pedigrees von Ullah, Ehsan, Mall, Raghvendra, Abbas, Mostafa M, Kunji, Khalid, Nato, Alejandro Q, Bensmail, Halima, Wijsman, Ellen M, Saad, Mohamad

Volltext

Post‐Genome‐Wide Association Study Challenges for Lipid Traits: Describing Age as a Modifier of Gene‐Lipid Associations in the Population Architecture Using Genomics and Epidemiolo... von Dumitrescu, Logan, Carty, Cara L., Franceschini, Nora, Hindorff, Lucia A., Cole, Shelley A., Bůžková, Petra, Schumacher, Fredrick R., Eaton, Charles B., Goodloe, Robert J., Duggan, David J., Haessler, Jeff, Cochran, Barbara, Henderson, Brian E., Cheng, Iona, Johnson, Karen C., Carlson, Chris S., Love, Shelly‐Ann, Brown‐Gentry, Kristin, Nato, Alejandro Q., Quibrera, Miguel, Anderson, Garnet, Shohet, Ralph V., Ambite, José Luis, Wilkens, Lynne R., Marchand, Loïc Le, Haiman, Christopher A., Buyske, Steven, Kooperberg, Charles, North, Kari E., Fornage, Myriam, Crawford, Dana C.

Volltext