A Whole-Genome Scan for Obstructive Sleep Apnea and Obesity by Palmer, Lyle J., Buxbaum, Sarah G., Larkin, Emma, Patel, Sanjay R., Elston, Robert C., Tishler, Peter V., Redline, Susan

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A Quantitative-Trait Analysis of Human Plasma–Dopamine β-Hydroxylase Activity: Evidence for a Major Functional Polymorphism at the DBH Locus by Zabetian, Cyrus P., Anderson, George M., Buxbaum, Sarah G., Elston, Robert C., Ichinose, Hiroshi, Nagatsu, Toshiharu, Kim, Kwang-Soo, Kim, Chun-Hyung, Malison, Robert T., Gelernter, Joel, Cubells, Joseph F.

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Adhesion molecules, endothelin-1 and lung function in seven population-based cohorts by Oelsner, E. C., Pottinger, T. D., Burkart, K. M., Allison, M., Buxbaum, S. G., Hansel, N. N., Kumar, R., Larkin, E. K., Lange, L. A., Loehr, L. R., London, S. J., O'Connor, G. T., Papanicolaou, G., Petrini, M. F., Rabinowitz, D., Raghavan, S., Redline, S., Thyagarajan, B., Tracy, R. P., Wilk, J. B., White, W. B., Rich, S. S., Barr, R. G.

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The Structure of Linkage Disequilibrium at the DBH Locus Strongly Influences the Magnitude of Association between Diallelic Markers and Plasma Dopamine β-Hydroxylase Activity by Zabetian, Cyrus P., Buxbaum, Sarah G., Elston, Robert C., Köhnke, Michael D., Anderson, George M., Gelernter, Joel, Cubells, Joseph F.

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Predicting Quantitative Trait Levels by Modeling SNP Interaction by Fijal, Bonnie A., Kim, Lee-Lian, Buxbaum, Sarah G., Witte, John S.

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A Single Nucleotide Polymorphism at DBH, Possibly Associated with Attention-Deficit/Hyperactivity Disorder, Associates with Lower Plasma Dopamine β-Hydroxylase Activity and is in L... by Tang, Yilang, Buxbaum, Sarah G., Waldman, Irwin, Anderson, George M., Zabetian, Cyrus P., Köhnke, Michael D., Cubells, Joseph F.

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Whole Genome Scan for Obstructive Sleep Apnea and Obesity in African-American Families by Palmer, Lyle J, Buxbaum, Sarah G, Larkin, Emma K, Patel, Sanjay R, Elston, Robert C, Tishler, Peter V, Redline, Susan

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Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13 by SHIBAMURA, Hidenori, OLSON, Jane M, LIMET, Raymond, MACKEAN, Gerald L, DEFAWE, Olivier, VERLOES, Alain, ARTHUR, Claudette, LOSSING, Alan G, BURNETT, Marjorie, SUEDA, Taijiro, KUIVANIEMI, Helena, VAN VLIJMEN-VAN KEULEN, Clarissa, BUXBAUM, Sarah G, DUDEK, Doreen M, TROMP, Gerard, OGATA, Toru, SKUNCA, Magdalena, SAKALIHASAN, Natzi, PALS, Gerard

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Genetics of the apnea hypopnea index in Caucasians and African Americans: I. Segregation analysis by Buxbaum, Sarah G., Elston, Robert C., Tishler, Peter V., Redline, Susan

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RESPONSE: Testing for Colon Neoplasia Susceptibility Variants at the Human COX2 Locus by Wiesner, Georgia L., Platzer, Petra, Buxbaum, Sarah G., Lewis, Susan, Macmillen, Melissa, Willis, Joseph, Chakravarti, Aravinda, Elston, Robert C., Markowitz, Sanfor D.

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Comparative Study of Multipoint Methods for Genotype Error Detection by Mukhopadhyay, Nandita, Buxbaum, Sarah G., Weeks, Daniel E.

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Testing for Colon Neoplasia Susceptibility Variants at the Human COX2 Locus by Ulrich, Cornelia M., Potter, John D.

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New genetic loci link adipose and insulin biology to body fat distribution by Ferreira, Teresa, Locke, Adam E., Justice, Anne E., Wu, Joseph M. W., Buchkovich, Martin L., Heard-Costa, Nancy L., Drong, Alexander W., Gustafsson, Stefan, Fall, Tove, Scherag, André, Absher, Devin, Ehret, Georg B., Kleber, Marcus E., Peters, Marjolein J., Albrecht, Eva, Bellis, Claire, Böhringer, Stefan, Böttcher, Yvonne, Clarke, Robert, Eklund, Niina, Erdos, Michael R., Estrada, Karol, Eury, Elodie, Friedrich, Nele, Giedraitis, Vilmantas, Gigante, Bruna, Go, Alan S., Hallmans, Goran, Hassinen, Maija, Hunt, Steven C., Koenig, Wolfgang, Kratzer, Wolfgang, Lindström, Jaana, Merger, Sigrun, Mihailov, Evelin, Mills, Rebecca, Moayyeri, Alireza, Müller-Nurasyid, Martina, Nalls, Michael A., Narisu, Narisu, Nolte, Ilja M., Sanna, Serena, Seufferlein, Thomas, Wennauer, Roman, Choi, Murim, Karpe, Fredrik, Keildson, Sarah, Kiryluk, Krzysztof, Lifton, Richard P., Ma, Baoshan, Nicholson, George, Schadt, Eric E., Scott, Robert A., Westra, Harm-Jan, Beilby, John, Bergman, Richard N., Brown, Morris J., Campbell, Harry, Danesh, John, de Geus, Eco J. C., Ferrannini, Ele, Ferrières, Jean, Haiman, Christopher A., Johansen, Berit, Jousilahti, Pekka, Keinanen-Kiukaanniemi, Sirkka M., Kooperberg, Charles, Kumari, Meena, Matise, Tara C., Möhlenkamp, Stefan, Nelis, Mari, Ong, Ken K., Palmer, Lyle J., Ritchie, Marylyn D., Salomaa, Veikko, Samani, Nilesh J., Saramies, Jouko, Sarzynski, Mark A., Schwarz, Peter E. H., Strauch, Konstantin, Boehm, Bernhard O., Chambers, John C., Grabe, Hans-Jörgen, Hamsten, Anders, Kivimaki, Mika, März, Winfried, Pedersen, Nancy L., Pérusse, Louis, Power, Chris, Rauramaa, Rainer, Rivadeneira, Fernando, Thorsteinsdottir, Unnur, Stumvoll, Michael, Watkins, Hugh, Wichmann, H-Erich, Hunter, David J., Qi, Lu, Speliotes, Elizabeth K., Fox, Caroline S., Barroso, Inês

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Synaptic, transcriptional and chromatin genes disrupted in autism by De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Ercument Cicek, A., Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas G., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Sean Hill, R., Ionita-Laza, Iuliana, Jimenez Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma’ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Jeremy Willsey, A., Yu, Timothy W., Yuen, Ryan K. C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.

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Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue by Bhalala, Oneil G, Nath, Artika P, Inouye, Michael, Sibley, Christopher R

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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders by Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Vorstman, Jacob A.S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bacchelli, Elena, Gallinger, Steven, Cotterchio, Michelle, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, Jiménez González, Patricia, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen W.

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Diagnosis of indeterminate biliary strictures (with videos) by Buxbaum, James

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Patterns and rates of exonic de novo mutations in autism spectrum disorders by Neale, Benjamin M., Kou, Yan, Liu, Li, Ma’ayan, Avi, Samocha, Kaitlin E., Sabo, Aniko, Lin, Chiao-Feng, Stevens, Christine, Wang, Li-San, Makarov, Vladimir, Polak, Paz, Yoon, Seungtai, Maguire, Jared, Crawford, Emily L., Campbell, Nicholas G., Geller, Evan T., Valladares, Otto, Schafer, Chad, Liu, Han, Zhao, Tuo, Cai, Guiqing, Lihm, Jayon, Dannenfelser, Ruth, Jabado, Omar, Peralta, Zuleyma, Nagaswamy, Uma, Muzny, Donna, Reid, Jeffrey G., Newsham, Irene, Wu, Yuanqing, Lewis, Lora, Han, Yi, Voight, Benjamin F., Lim, Elaine, Rossin, Elizabeth, Kirby, Andrew, Flannick, Jason, Fromer, Menachem, Shakir, Khalid, Fennell, Tim, Garimella, Kiran, Banks, Eric, Poplin, Ryan, Gabriel, Stacey, DePristo, Mark, Wimbish, Jack R., Boone, Braden E., Levy, Shawn E., Betancur, Catalina, Sunyaev, Shamil, Boerwinkle, Eric, Buxbaum, Joseph D., Cook Jr, Edwin H., Devlin, Bernie, Gibbs, Richard A., Roeder, Kathryn, Schellenberg, Gerard D., Sutcliffe, James S., Daly, Mark J.

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American Society for Gastrointestinal Endoscopy guideline on post-ERCP pancreatitis prevention strategies: summary and recommendations by Buxbaum, James L., Freeman, Martin, Amateau, Stuart K., Chalhoub, Jean M., Coelho-Prabhu, Nayantara, Desai, Madhav, Elhanafi, Sherif E., Forbes, Nauzer, Fujii-Lau, Larissa L., Kohli, Divyanshoo R., Kwon, Richard S., Machicado, Jorge D., Marya, Neil B., Pawa, Swati, Ruan, Wenly H., Sheth, Sunil G., Thiruvengadam, Nikhil R., Thosani, Nirav C., Qumseya, Bashar J.

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Blastic plasmacytoid dendritic cell neoplasm in children: diagnostic features and clinical implications by JEGALIAN, Armin G, BUXBAUM, Nataliya P, FACCHETTI, Fabio, RAFFELD, Mark, PITTALUGA, Stefania, WAYNE, Alan S, JAFFE, Elaine S

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