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

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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

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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

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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.

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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.

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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.

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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.

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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

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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.

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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

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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

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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.

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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

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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.

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Estimating relationships between phenotypes and subjects drawn from admixed families von Blue, Elizabeth M, Brown, Lisa A, Conomos, Matthew P, Kirk, Jennifer L, Nato, Jr, Alejandro Q, Popejoy, Alice B, Raffa, Jesse, Ranola, John, Wijsman, Ellen M, Thornton, Timothy

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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

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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

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No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population 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-Anne, Brown-Gentry, Kristin, Nato, Alejandro Q., Quibrera, Miguel, Shohet, Ralph V., Ambite, José Luis, Wilkens, Lynne R., Le Marchand, Loïc, Haiman, Christopher A., Buyske, Steven, Kooperberg, Charles, North, Kari E., Fornage, Myriam, Crawford, Dana C.

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Single-Variant and Multi-Variant Trend Tests for Genetic Association with Next-Generation Sequencing That Are Robust to Sequencing Error von Kim, Wonkuk, Londono, Douglas, Zhou, Lisheng, Xing, Jinchuan, Nato, Alejandro Q., Musolf, Anthony, Matise, Tara C., Finch, Stephen J., Gordon, Derek

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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

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