Providing Pediatric Subspecialty Care: A Workforce Analysis by Stoddard, Jeffrey J, Cull, William L, Jewett, Ethan A. B, Brotherton, Sarah E, Mulvey, Holly J, Alden, Errol R, AAP Committee on Pediatric Workforce Subcommittee on Subspecialty Workforce

Get full text

Pediatric Residency Education by Mulvey, Holly J, Ogle-Jewett, Ethan A. B, Cheng, Tina L, Johnson, Robert L

Get full text

An Exposure-Wide and Mendelian Randomization Approach to Identifying Modifiable Factors for the Prevention of Depression by Choi, Karmel W, Stein, Murray B, Nishimi, Kristen M, Ge, Tian, Coleman, Jonathan R.I, Chen, Chia-Yen, Ratanatharathorn, Andrew, Zheutlin, Amanda B, Dunn, Erin C, Breen, Gerome, Koenen, Karestan C, Smoller, Jordan W

Get full text

Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations by Thorpe, Hayley H A, Fontanillas, Pierre, Pham, Benjamin K, Meredith, John J, Jennings, Mariela V, Courchesne-Krak, Natasia S, Vilar-Ribó, Laura, Bianchi, Sevim B, Mutz, Julian, Elson, Sarah L, Khokhar, Jibran Y, Abdellaoui, Abdel, Davis, Lea K, Palmer, Abraham A, Sanchez-Roige, Sandra

Get full text

Loci associated with skin pigmentation identified in African populations by Crawford, Nicholas G., Kelly, Derek E., Hansen, Matthew E. B., Beltrame, Marcia H., Fan, Shaohua, Bowman, Shanna L., Jewett, Ethan, Ranciaro, Alessia, Thompson, Simon, Lo, Yancy, Pfeifer, Susanne P., Jensen, Jeffrey D., Campbell, Michael C., Beggs, William, Hormozdiari, Farhad, Mpoloka, Sununguko Wata, Mokone, Gaonyadiwe George, Nyambo, Thomas, Meskel, Dawit Wolde, Belay, Gurja, Haut, Jake, NISC Comparative Sequencing Program, Rothschild, Harriet, Zon, Leonard, Zhou, Yi, Kovacs, Michael A., Xu, Mai, Zhang, Tongwu, Bishop, Kevin, Sinclair, Jason, Rivas, Cecilia, Elliot, Eugene, Choi, Jiyeon, Li, Shengchao A., Hicks, Belynda, Burgess, Shawn, Abnet, Christian, Watkins-Chow, Dawn E., Oceana, Elena, Song, Yun S., Eskin, Eleazar, Brown, Kevin M., Marks, Michael S., Loftus, Stacie K., Pavan, William J., Yeager, Meredith, Chanock, Stephen, Tishkoff, Sarah A.

Get full text

Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects by Krohn, Lynne, Heilbron, Karl, Blauwendraat, Cornelis, Reynolds, Regina H., Yu, Eric, Senkevich, Konstantin, Rudakou, Uladzislau, Estiar, Mehrdad A., Gustavsson, Emil K., Brolin, Kajsa, Ruskey, Jennifer A., Freeman, Kathryn, Asayesh, Farnaz, Chia, Ruth, Arnulf, Isabelle, Hu, Michele T. M., Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Šonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Biscarini, Francesco, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Scholz, Sonja W., Ryten, Mina, Bandres-Ciga, Sara, Noyce, Alastair, Cannon, Paul, Pihlstrøm, Lasse, Nalls, Mike A., Singleton, Andrew B., Rouleau, Guy A., Postuma, Ronald B., Gan-Or, Ziv

Get full text

Analysis of rare Parkinson’s disease variants in millions of people by Pitz, Vanessa, Makarious, Mary B., Bandres-Ciga, Sara, Iwaki, Hirotaka, Singleton, Andrew B., Nalls, Mike, Heilbron, Karl, Blauwendraat, Cornelis

Get full text

The Parkinson's Disease Mendelian Randomization Research Portal by Noyce, Alastair J., Bandres‐Ciga, Sara, Kim, Jonggeol, Heilbron, Karl, Kia, Demis, Hemani, Gibran, Xue, Angli, Lawlor, Debbie A., Smith, George Davey, Duran, Raquel, Gan‐Or, Ziv, Blauwendraat, Cornelis, Gibbs, J. Raphael, Hinds, David A., Yang, Jian, Visscher, Peter, Cuzick, Jack, Morris, Huw, Hardy, John, Wood, Nicholas W., Nalls, Mike A., Singleton, Andrew B.

Get full text

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders by Strom, Nora I., Halvorsen, Matthew W., Grove, Jakob, Ásbjörnsdóttir, Bergrún, Thorarensen, Ólafur, de Schipper, Elles, Bäckmann, Julia, Tian, Chao, Sul, Jae Hoon, Tsetsos, Fotis, Zelaya, Ivette, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Barr, Cathy L., Grados, Marco, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Lyon, Gholson J., McMahon, William M., Batterson, James R., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Hoekstra, Pieter J., Zinner, Samuel H., Luðvigsson, Pétur, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N., Knowles, James A., Buckner, Randy L., Willsey, Jeremy A., Tischfield, Jay A., Heiman, Gary A., Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Pauls, David L., Freimer, Nelson B., Davis, Lea K., Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Agee, Michelle, Auton, Adam, Elson, Sarah L., Furlotte, Nicholas A., Hicks, Barry, Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K., McIntyre, Matthew H., McManus, Kimberly F., Mountain, Joanna L., Pitts, Steven J., Poznik, G. David, Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tung, Joyce Y., Wang, Xin, Als, Thomas Damm, Meier, Sandra M., Bybjerg-Grauholm, Jonas, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Hinds, David A., Rück, Christian, Mataix-Cols, David, Mattheisen, Manuel

Get full text

CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice by Sanchez-Roige, Sandra, Jennings, Mariela V., Thorpe, Hayley H. A., Mallari, Jazlene E., van der Werf, Lieke C., Bianchi, Sevim B., Huang, Yuye, Lee, Calvin, Mallard, Travis T., Barnes, Samuel A., Wu, Jin Yi, Barkley-Levenson, Amanda M., Boussaty, Ely C., Snethlage, Cedric E., Schafer, Danielle, Babic, Zeljana, Winters, Boyer D., Watters, Katherine E., Biederer, Thomas, Mackillop, James, Stephens, David N., Elson, Sarah L., Fontanillas, Pierre, Khokhar, Jibran Y., Young, Jared W., Palmer, Abraham A.

Get full text

MLH1 Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families by BORRAS, Ester, PINEDA, Marta, BALMANA, Judith, TORRES, Asunción, RAMON Y CAJAL, Teresa, SANZ, Judit, PEREZ-CABORNERO, Lucia, CASTELLVI-BEL, Sergi, ALONSO, Angel, LANAS, Angel, GONZALEZ, Sara, MORENO, Victor, BLANCO, Ignacio, GRUBER, Stephen B, ROSENBERG, Noah A, MUKHERJEE, Bhramar, LAZARO, Conxi, CAPELLA, Gabriel, JEWETT, Ethan M, FEI WANG, TEULE, Alex, CALDES, Trinidad, URIOSTE, Miguel, MARTINEZ-BOUZAS, Cristina, BRUNET, Joan

Get full text

A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals by Jennings, Mariela V., Martínez-Magaña, José Jaime, Courchesne-Krak, Natasia S., Cupertino, Renata B., Vilar-Ribó, Laura, Bianchi, Sevim B., Hatoum, Alexander S., Atkinson, Elizabeth G., Giusti-Rodriguez, Paola, Montalvo-Ortiz, Janitza L., Gelernter, Joel, Artigas, María Soler, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan, Lin, Keng-Han, Llamas, Bianca A., Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Nandakumar, Priyanka, Nguyen, Dominique T., Noblin, Elizabeth S., O'Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Reynoso, Alexandra, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Su, Qiaojuan Jane, Tat, Susana A., Tchakouté, Christophe Toukam, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Wong, Corinna D., Elson, Sarah L., Edenberg, Howard J., Fontanillas, Pierre, Palmer, Abraham A., Sanchez-Roige, Sandra

Get full text

The genetic architecture of dog ownership: large-scale genome-wide association study in 97,552 European-ancestry individuals by Gong, Tong, Karlsson, Robert, Yao, Shuyang, Magnusson, Patrik K E, Ajnakina, Olesya, Steptoe, Andrew, Bhatta, Laxmi, Brumpton, Ben, Kumar, Ashish, Mélen, Erik, Lin, Keng-Han, Tian, Chao, Fall, Tove, Almqvist, Catarina

Get full text