Defining the role of the MHC in autoimmunity: a review and pooled analysis by Fernando, Michelle M A, Stevens, Christine R, Walsh, Emily C, De Jager, Philip L, Goyette, Philippe, Plenge, Robert M, Vyse, Timothy J, Rioux, John D

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Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism by Chahrour, Maria H, Yu, Timothy W, Lim, Elaine T, Ataman, Bulent, Coulter, Michael E, Hill, R Sean, Stevens, Christine R, Schubert, Christian R, Greenberg, Michael E, Gabriel, Stacey B, Walsh, Christopher A

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Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome by Manzini, M. Chiara, Tambunan, Dimira E., Hill, R. Sean, Yu, Tim W., Maynard, Thomas M., Heinzen, Erin L., Shianna, Kevin V., Stevens, Christine R., Partlow, Jennifer N., Barry, Brenda J., Rodriguez, Jacqueline, Gupta, Vandana A., Al-Qudah, Abdel-Karim, Eyaid, Wafaa M., Friedman, Jan M., Salih, Mustafa A., Clark, Robin, Moroni, Isabella, Mora, Marina, Beggs, Alan H., Gabriel, Stacey B., Walsh, Christopher A.

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Identification of two independent risk factors for lupus within the MHC in United Kingdom families by Fernando, Michelle M A, Stevens, Christine R, Sabeti, Pardis C, Walsh, Emily C, McWhinnie, Alasdair J M, Shah, Anila, Green, Todd, Rioux, John D, Vyse, Timothy J

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Using Whole-Exome Sequencing to Identify Inherited Causes of Autism by Yu, Timothy W., Chahrour, Maria H., Coulter, Michael E., Jiralerspong, Sarn, Okamura-Ikeda, Kazuko, Ataman, Bulent, Schmitz-Abe, Klaus, Harmin, David A., Adli, Mazhar, Malik, Athar N., D’Gama, Alissa M., Lim, Elaine T., Sanders, Stephan J., Mochida, Ganesh H., Partlow, Jennifer N., Sunu, Christine M., Felie, Jillian M., Rodriguez, Jacqueline, Nasir, Ramzi H., Ware, Janice, Joseph, Robert M., Hill, R. Sean, Kwan, Benjamin Y., Al-Saffar, Muna, Mukaddes, Nahit M., Hashmi, Asif, Balkhy, Soher, Gascon, Generoso G., Hisama, Fuki M., LeClair, Elaine, Poduri, Annapurna, Oner, Ozgur, Al-Saad, Samira, Al-Awadi, Sadika A., Bastaki, Laila, Ben-Omran, Tawfeg, Teebi, Ahmad S., Al-Gazali, Lihadh, Eapen, Valsamma, Stevens, Christine R., Rappaport, Leonard, Gabriel, Stacey B., Markianos, Kyriacos, State, Matthew W., Greenberg, Michael E., Taniguchi, Hisaaki, Braverman, Nancy E., Morrow, Eric M., Walsh, Christopher A.

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Evolution of Osteocrin as an activity-regulated factor in the primate brain by Ataman, Bulent, Boulting, Gabriella L, Harmin, David A, Yang, Marty G, Baker-Salisbury, Mollie, Yap, Ee-Lynn, Malik, Athar N, Mei, Kevin, Rubin, Alex A, Spiegel, Ivo, Durresi, Ershela, Sharma, Nikhil, Hu, Linda S, Pletikos, Mihovil, Griffith, Eric C, Partlow, Jennifer N, Stevens, Christine R, Adli, Mazhar, Chahrour, Maria, Sestan, Nenad, Walsh, Christopher A, Berezovskii, Vladimir K, Livingstone, Margaret S, Greenberg, Michael E

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CHARR efficiently estimates contamination from DNA sequencing data by Lu, Wenhan, Gauthier, Laura D., Poterba, Timothy, Giacopuzzi, Edoardo, Goodrich, Julia K., Stevens, Christine R., King, Daniel, Daly, Mark J., Neale, Benjamin M., Karczewski, Konrad J.

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PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features by Khalil, Raida, Kenny, Connor, Hill, R. Sean, Mochida, Ganeshwaran H., Nasir, Ramzi, Partlow, Jennifer N., Barry, Brenda J., Al‐Saffar, Muna, Egan, Chloe, Stevens, Christine R., Gabriel, Stacey B., Barkovich, A. James, Ellison, Jay W., Al‐Gazali, Lihadh, Walsh, Christopher A., Chahrour, Maria H.

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SMAD3 gene variant is a risk factor for recurrent surgery in patients with Crohn's disease by Fowler, Sharyle A., Ananthakrishnan, Ashwin N., Gardet, Agnes, Stevens, Christine R., Korzenik, Joshua R., Sands, Bruce E., Daly, Mark J., Xavier, Ramnik J., Yajnik, Vijay

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Established genetic risk factors do not distinguish early and later onset Crohn's disease by Essers, Jonah B., Lee, Jessica J., Kugathasan, Subra, Stevens, Christine R., Grand, Richard J., Daly, Mark J.

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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, Cicek, A Erucment, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarinder, Klei, Lambertus, Kosmicki, Jack, Shih-Chen, Fu, 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, Curran, Sarah R, Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A, Gallagher, Louise, Geller, Evan, Guter, Stephen J, Hill, R Sean, Ionita-Laza, Juliana, Jimenz Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M, Kolevzon, Alexander, Lee, Irene, Lei, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R, McInnes, Alison L, Neale, Benjamin, Owen, Michael J, Ozaki, Noriio, 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, Li-San, Wang, Weiss, Lauren A, Willsey, A Jeremy, Yu, Timothy W, Yuen, Ryan K C, Cook, Edwin H, Freitag, Christine M, Gill, Michael, Hultman, Christina M, Lehner, Thomas, Palotie, Aaarno, Schellenberg, Gerard D, Sklar, Pamela, State, Matthew W, Sutcliffe, James S, Walsh, Christiopher A, Scherer, Stephen W, Zwick, Michael E, Barett, Jeffrey C, Cutler, David J, Roeder, Kathryn, Devlin, Bernie, Daly, Mark J, Buxbaum, Joseph D

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Rare coding variants in ten genes confer substantial risk for schizophrenia by Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D, Bigdeli, Tim B, Breen, Gerome, Buckley, Peter F, Bunney, William E, Bybjerg-Grauholm, Jonas, Chapman, Sinéad B, Chen, Wei J, Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M, DeLisi, Lynn, Dodge, Sheila, Eskelinen, Saana, Fanous, Ayman H, Faraone, Stephen V, Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B, Gage, Diane, Gagliano Taliun, Sarah A, Ganna, Andrea, Genovese, Giulio, Glahn, David C, Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O, Holi, Matti, Hougaard, David M, Howrigan, Daniel P, Huang, Hailiang, Kahn, René S, Kang, Hyun Min, Karczewski, Konrad J, Kirov, George, Knowles, James A, Lee, Francis S, Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R, McCarroll, Steven A, Medeiros, Helena, Milani, Lili, Morley, Christopher P, Morris, Derek W, Mortensen, Preben Bo, Myers, Richard M, Nordentoft, Merete, O'Brien, Niamh L, Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H, Palmer, Duncan S, Paunio, Tiina, Quested, Digby, Rapaport, Mark H, Rees, Elliott, Rollins, Brandi, Satterstrom, F Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J, Sharp, Sally I, Sklar, Pamela, Smoller, Jordan W, Sobell, Janet L, Solomonson, Matthew, Stahl, Eli A, Stevens, Christine R, Tiao, Grace, Watson, Stanley J, Watts, Nicholas A, Blackwood, Douglas H, Cohen, Bruce M, Corvin, Aiden P, Esko, Tõnu, Freimer, Nelson B, Glatt, Stephen J, Hultman, Christina M, McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N, Pato, Michele T, Pulver, Ann E, St Clair, David, Tsuang, Ming T, Vawter, Marquis P, Walters, James T, Werge, Thomas M, Ophoff, Roel A, Sullivan, Patrick F, Owen, Michael J, O'Donovan, Michael C, Neale, Benjamin M, Daly, Mark J

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Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease by Walker, Gareth J, Harrison, James W, Heap, Graham A, Voskuil, Michiel D, Andersen, Vibeke, Anderson, Carl A, Ananthakrishnan, Ashwin N, Barrett, Jeffrey C, Beaugerie, Laurent, Bewshea, Claire M, Cole, Andy T, Cummings, Fraser R, Daly, Mark J, Ellul, Pierre, Fedorak, Richard N, Festen, Eleonora A. M, Florin, Timothy H, Gaya, Daniel R, Halfvarson, Jonas, Hart, Ailsa L, Heerasing, Neel M, Hendy, Peter, Irving, Peter M, Jones, Samuel E, Koskela, Jukka, Lindsay, James O, Mansfield, John C, McGovern, Dermot, Parkes, Miles, Pollok, Richard C. G, Ramakrishnan, Subramaniam, Rampton, David S, Rivas, Manuel A, Russell, Richard K, Schultz, Michael, Sebastian, Shaji, Seksik, Philippe, Singh, Abhey, So, Kenji, Sokol, Harry, Subramaniam, Kavitha, Todd, Anthony, Annese, Vito, Weersma, Rinse K, Xavier, Ramnik, Ward, Rebecca, Weedon, Michael N, Goodhand, James R, Kennedy, Nicholas A, Ahmad, Tariq

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Rare coding variants in 10 genes confer substantial risk for schizophrenia by Singh, Tarjinder, Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D., Bass, Nicholas, Bigdeli, Tim B., Breen, Gerome, Bromet, Evelyn J., Buckley, Peter F., Bunney, William E., Bybjerg-Grauholm, Jonas, Byerley, William F., Chapman, Sinéad B., Chen, Wei J., Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M., DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A., Eskelinen, Saana, Fanous, Ayman H., Faraone, Stephen V., Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B., Gage, Diane, Taliun, Sarah A. Gagliano, Ganna, Andrea, Genovese, Giulio, Glahn, David C., Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O., Holi, Matti, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Hwu, Hai-Gwo, Kahn, René S., Kang, Hyun Min, Karczewski, Konrad J., Kirov, George, Knowles, James A., Lee, Francis S., Lehrer, Douglas S., Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R., McCarroll, Steven A., McIntosh, Andrew M., Medeiros, Helena, Milani, Lili, Morley, Christopher P., Morris, Derek W., Bo Mortensen, Preben, Myers, Richard M., Nordentoft, Merete, O’Brien, Niamh L., Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H., Palmer, Duncan S., Paunio, Tiina, Quested, Digby, Rapaport, Mark H., Rees, Elliott, Rollins, Brandi, Satterstrom, F. Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J., Sharp, Sally I., Sklar, Pamela, Smoller, Jordan W., Sobell, Janet l., Solomonson, Matthew, Stevens, Christine R., Suvisaari, Jaana, Tiao, Grace, Watson, Stanley J., Watts, Nicholas A., Blackwood, Douglas H., Børglum, Anders D., Cohen, Bruce M., Corvin, Aiden P., Esko, Tõnu, Freimer, Nelson B., Glatt, Stephen J., Hultman, Christina M., McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N., Pato, Michele T., Pulver, Ann E., St. Clair, David, Tsuang, Ming T.

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Evolution of Osteocrin as an activityregulated factor in the primate brain by Ataman, Bulent, Boulting, Gabriella L, Harmin, David A, Yang, Marty G, Baker-Salisbury, Mollie, Yap, Ee-Lynn, Malik, Athar N, Mei, Kevin, Rubin, Alex A, Spiegel, Ivo, Durresi, Ershela, Sharma, Nikhil, Hu, Linda S, Pletikos, Mihovil, Griffith, Eric C, Partlow, Jennifer N, Stevens, Christine R, Adli, Mazhar, Chahrour, Maria, Sestan, Nenad, Walsh, Christopher A, Berezovskii, Vladimir K, Livingstone, Margaret S, Greenberg, Michael E

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Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis: e1000024 by Fernando, Michelle MA, Stevens, Christine R, Walsh, Emily C, Jager, Philip LDe, Goyette, Philippe, Plenge, Robert M, Vyse, Timothy J, Rioux, John D

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Identification of Two Independent Risk Factors for Lupus within the MHC in UK Families by Fernando, Michelle M. A., Stevens, Christine R., Sabeti, Pardis Christine, Walsh, Emily C., McWhinnie, Alasdair J.M., Shah, Anila, Green, Todd, Rioux, John D., Vyse, Timothy J

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UNTANGLING THE FMLA by Engbarth, Fred, Stevens, Christine R

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Evolution of Retinal Detachment in Posterior Retinopathy of Prematurity: Impact on Treatment Approach by Vinekar, Anand, Trese, Michael T, Capone, Antonio

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Nurses' experience with the clinical application of a research-based nursing protocol in a long-term care setting by Simpson, Michelle R, Stevens, Patricia, Kovach, Christine R

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