Physical Findings and the Risk for Obstructive Sleep Apnea . The Importance of Oropharyngeal Structures von SCHELLENBERG, JOSEPH B, MAISLIN, GREG, SCHWAB, RICHARD J

Volltext

Assessing tumor heterogeneity: integrating tissue and circulating tumor DNA (ctDNA) analysis in the era of immuno-oncology - blood TMB is not the same as tissue TMB von Fridland, Stanislav, Choi, Jaeyoun, Nam, Myungwoo, Schellenberg, Samuel Joseph, Kim, Eugene, Lee, Grace, Yoon, Nathaniel, Chae, Young Kwang

Volltext

ACUTE EOSINOPHILIC PNUEMONIA ATTRIBUTED TO BALASALZIDE von DALLAROSA, JOHN, SOLLER, DYLAN, SCHELLENBERG, JOSEPH

Volltext

A CASE OF PULMONARY AMYLOIDOSIS WITH PROGRESSIVE SYSTEMIC INVOLVEMENT von GOYAL, SALONI, SIU, CHUN, KHASKIA, YASMEEN, SCHELLENBERG, JOSEPH

Volltext

THE UNFORUNATE SEEDING OF TESTICULAR CHORIOCARCINOIMA FOLLOWING THE FONTAN PROCEDURE von DELATORRE, MARTIN, AHLUWALIA, ARJAN, ZHU, ALINA, MUSCO, KAITLYN, SCHELLENBERG, JOSEPH

Volltext

A CASE OF HÜRTHLE CELL CARCINOMA PRESENTING WITH MALIGNANT PLEURAL EFFUSION von GOYAL, SALONI, ZARINA REYES, CLEO, PETRENKO, DIMITRY, SCHELLENBERG, JOSEPH

Volltext

DOUBLE RARITY: A CASE OF ACTINOMYCES IN PULMONARY SEQUESTRATION von FISHER, MEGAN, SOLLER, DYLAN, KHASKIA, YASMEEN, SCHELLENBERG, JOSEPH

Volltext

NECROTIZING GRANULOMAS IN A CONSTRUCTION WORKER von Soller, Dylan, Lenivy, Christopher, Musco, Kaitlyn, Schellenberg, Joseph

Volltext

Current and future role of double-lung transplantation for bilateral lung cancer von Lee, Jeeyeon, Schellenberg, Samuel J., Chung, Liam Il-Young, Bharat, Ankit, Chae, Young Kwang

Volltext

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes von He, Xin, Sanders, Stephan J, Liu, Li, De Rubeis, Silvia, Lim, Elaine T, Sutcliffe, James S, Schellenberg, Gerard D, Gibbs, Richard A, Daly, Mark J, Buxbaum, Joseph D, State, Matthew W, Devlin, Bernie, Roeder, Kathryn

Volltext

A framework for the interpretation of de novo mutation in human disease von Samocha, Kaitlin E, Robinson, Elise B, Sanders, Stephan J, Stevens, Christine, Sabo, Aniko, McGrath, Lauren M, Kosmicki, Jack A, Rehnström, Karola, Mallick, Swapan, Kirby, Andrew, Wall, Dennis P, MacArthur, Daniel G, Gabriel, Stacey B, DePristo, Mark, Purcell, Shaun M, Palotie, Aarno, Boerwinkle, Eric, Buxbaum, Joseph D, Cook, Edwin H, Gibbs, Richard A, Schellenberg, Gerard D, Sutcliffe, James S, Devlin, Bernie, Roeder, Kathryn, Neale, Benjamin M, Daly, Mark J

Volltext

Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria von Höglinger, Günter U., Respondek, Gesine, Stamelou, Maria, Kurz, Carolin, Josephs, Keith A., Lang, Anthony E., Mollenhauer, Brit, Müller, Ulrich, Nilsson, Christer, Whitwell, Jennifer L., Arzberger, Thomas, Englund, Elisabet, Gelpi, Ellen, Giese, Armin, Irwin, David J., Meissner, Wassilios G., Pantelyat, Alexander, Rajput, Alex, Swieten, John C., Troakes, Claire, Antonini, Angelo, Bhatia, Kailash P., Bordelon, Yvette, Compta, Yaroslau, Corvol, Jean‐Christophe, Colosimo, Carlo, Dickson, Dennis W., Dodel, Richard, Ferguson, Leslie, Grossman, Murray, Kassubek, Jan, Krismer, Florian, Levin, Johannes, Lorenzl, Stefan, Morris, Huw R., Nestor, Peter, Oertel, Wolfgang H., Poewe, Werner, Rabinovici, Gil, Rowe, James B., Schellenberg, Gerard D., Seppi, Klaus, Eimeren, Thilo, Wenning, Gregor K., Boxer, Adam L., Golbe, Lawrence I., Litvan, Irene, Boxer, Adam L., Rajput, Alex, Pantelyat, Alexander, Antonini, Angelo, Lang, Anthony E., Giese, Armin, Mollenhauer, Brit, Colosimo, Carlo, Kurz, Caroline, Nilsson, Christer, Troakes, Claire, Irwin, David J., Dickson, Dennis W., Gelpi, Ellen, Krismer, Florian, Schellenberg, Gerard D., Respondek, Gesine, Rabinovici, Gil, Wenning, Gregor K., Höglinger, Günter U., Morris, Huw R., Litvan, Irene, Rowe, James B., Kassubek, Jan, Corvol, Jean‐Christophe, Whitwell, Jennifer L., Levin, Johannes, van Swieten, John, Bhatia, Kailash P., Josephs, Keith A., Seppi, Klaus, Golbe, Lawrence I., Stamelou, Maria, Grossman, Murray, Nestor, Peter, Dodel, Richard, Lorenzl, Stefan, van Eimeren, Thilo, Arzberger, Thomas, Müller, Ulrich, Meissner, Wassilios G., Poewe, Werner, Oertel, Wolfgang H., Compta, Yaroslau, Bordelon, Yvette

Volltext

Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders von Lim, Elaine T., Raychaudhuri, Soumya, Sanders, Stephan J., Stevens, Christine, Sabo, Aniko, MacArthur, Daniel G., Neale, Benjamin M., Kirby, Andrew, Ruderfer, Douglas M., Fromer, Menachem, Lek, Monkol, Liu, Li, Flannick, Jason, Ripke, Stephan, Nagaswamy, Uma, Muzny, Donna, Reid, Jeffrey G., Hawes, Alicia, Newsham, Irene, Wu, Yuanqing, Lewis, Lora, Dinh, Huyen, Gross, Shannon, Wang, Li-San, Lin, Chiao-Feng, Valladares, Otto, Gabriel, Stacey B., dePristo, Mark, Altshuler, David M., Purcell, Shaun M., State, Matthew W., Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Gibbs, Richard A., Schellenberg, Gerard D., Sutcliffe, James S., Devlin, Bernie, Roeder, Kathryn, Daly, Mark J.

Volltext

Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants von Rehker, Jan, Rodhe, Johanna, Nesbitt, Ryan R, Boyle, Evan A, Martin, Beth K, Lord, Jenny, Karaca, Ilker, Naj, Adam, Jessen, Frank, Helisalmi, Seppo, Soininen, Hilkka, Hiltunen, Mikko, Ramirez, Alfredo, Scherer, Martin, Farrer, Lindsay A, Haines, Jonathan L, Pericak-Vance, Margaret A, Raskind, Wendy H, Cruchaga, Carlos, Schellenberg, Gerard D, Joseph, Bertrand, Brkanac, Zoran

Volltext

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls von Liu, Li, Sabo, Aniko, Neale, Benjamin M, Nagaswamy, Uma, Stevens, Christine, Lim, Elaine, Bodea, Corneliu A, Muzny, Donna, Reid, Jeffrey G, Banks, Eric, Coon, Hillary, Depristo, Mark, Dinh, Huyen, Fennel, Tim, Flannick, Jason, Gabriel, Stacey, Garimella, Kiran, Gross, Shannon, Hawes, Alicia, Lewis, Lora, Makarov, Vladimir, Maguire, Jared, Newsham, Irene, Poplin, Ryan, Ripke, Stephan, Shakir, Khalid, Samocha, Kaitlin E, Wu, Yuanqing, Boerwinkle, Eric, Buxbaum, Joseph D, Cook, Jr, Edwin H, Devlin, Bernie, Schellenberg, Gerard D, Sutcliffe, James S, Daly, Mark J, Gibbs, Richard A, Roeder, Kathryn

Volltext

Common genetic variants on 5p14.1 associate with autism spectrum disorders von Wang, Kai, Zhang, Haitao, Ma, Deqiong, Bucan, Maja, Glessner, Joseph T., Abrahams, Brett S., Salyakina, Daria, Imielinski, Marcin, Bradfield, Jonathan P., Sleiman, Patrick M. A., Kim, Cecilia E., Hou, Cuiping, Frackelton, Edward, Chiavacci, Rosetta, Takahashi, Nagahide, Sakurai, Takeshi, Rappaport, Eric, Lajonchere, Clara M., Munson, Jeffrey, Estes, Annette, Korvatska, Olena, Piven, Joseph, Sonnenblick, Lisa I., Alvarez Retuerto, Ana I., Herman, Edward I., Dong, Hongmei, Hutman, Ted, Sigman, Marian, Ozonoff, Sally, Klin, Ami, Owley, Thomas, Sweeney, John A., Brune, Camille W., Cantor, Rita M., Bernier, Raphael, Gilbert, John R., Cuccaro, Michael L., McMahon, William M., Miller, Judith, State, Matthew W., Wassink, Thomas H., Coon, Hilary, Levy, Susan E., Schultz, Robert T., Nurnberger, John I., Haines, Jonathan L., Sutcliffe, James S., Cook, Edwin H., Minshew, Nancy J., Buxbaum, Joseph D., Dawson, Geraldine, Grant, Struan F. A., Geschwind, Daniel H., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Hakonarson, Hakon

Volltext

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes von Glessner, Joseph T., Wang, Kai, Cai, Guiqing, Korvatska, Olena, Kim, Cecilia E., Wood, Shawn, Zhang, Haitao, Estes, Annette, Brune, Camille W., Bradfield, Jonathan P., Imielinski, Marcin, Frackelton, Edward C., Reichert, Jennifer, Crawford, Emily L., Munson, Jeffrey, Sleiman, Patrick M. A., Chiavacci, Rosetta, Annaiah, Kiran, Thomas, Kelly, Hou, Cuiping, Glaberson, Wendy, Flory, James, Otieno, Frederick, Garris, Maria, Soorya, Latha, Klei, Lambertus, Piven, Joseph, Meyer, Kacie J., Anagnostou, Evdokia, Sakurai, Takeshi, Game, Rachel M., Rudd, Danielle S., Zurawiecki, Danielle, McDougle, Christopher J., Davis, Lea K., Miller, Judith, Posey, David J., Michaels, Shana, Kolevzon, Alexander, Silverman, Jeremy M., Bernier, Raphael, Levy, Susan E., Schultz, Robert T., Dawson, Geraldine, Owley, Thomas, McMahon, William M., Wassink, Thomas H., Sweeney, John A., Nurnberger, John I., Coon, Hilary, Sutcliffe, James S., Minshew, Nancy J., Grant, Struan F. A., Bucan, Maja, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Schellenberg, Gerard D., Hakonarson, Hakon

Volltext

Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4,and the Risk of Late-Onset Alzheimer Disease in African Americans von Reitz, Christiane, Jun, Gyungah, Naj, Adam, Rajbhandary, Ruchita, Vardarajan, Badri Narayan, Wang, Li-San, Valladares, Otto, Lin, Chiao-Feng, Larson, Eric B, Graff-Radford, Neill R, Evans, Denis, De Jager, Philip L, Crane, Paul K, Buxbaum, Joseph D, Murrell, Jill R, Raj, Towfique, Ertekin-Taner, Nilufer, Logue, Mark, Baldwin, Clinton T, Green, Robert C, Barnes, Lisa L, Cantwell, Laura B, Fallin, M. Daniele, Go, Rodney C. P, Griffith, Patrick, Obisesan, Thomas O, Manly, Jennifer J, Lunetta, Kathryn L, Kamboh, M. Ilyas, Lopez, Oscar L, Bennett, David A, Hendrie, Hugh, Hall, Kathleen S, Goate, Alison M, Byrd, Goldie S, Kukull, Walter A, Foroud, Tatiana M, Haines, Jonathan L, Farrer, Lindsay A, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Mayeux, Richard

Volltext

Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants von Zou, Fanggeng, Chai, High Seng, Younkin, Curtis S, Allen, Mariet, Crook, Julia, Pankratz, V Shane, Carrasquillo, Minerva M, Rowley, Christopher N, Nair, Asha A, Middha, Sumit, Maharjan, Sooraj, Nguyen, Thuy, Ma, Li, Malphrus, Kimberly G, Palusak, Ryan, Lincoln, Sarah, Bisceglio, Gina, Georgescu, Constantin, Kouri, Naomi, Kolbert, Christopher P, Jen, Jin, Haines, Jonathan L, Mayeux, Richard, Pericak-Vance, Margaret A, Farrer, Lindsay A, Schellenberg, Gerard D, Petersen, Ronald C, Graff-Radford, Neill R, Dickson, Dennis W, Younkin, Steven G, Ertekin-Taner, Nilüfer

Volltext

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes von Bucan, Maja, Abrahams, Brett S, Wang, Kai, Glessner, Joseph T, Herman, Edward I, Sonnenblick, Lisa I, Alvarez Retuerto, Ana I, Imielinski, Marcin, Hadley, Dexter, Bradfield, Jonathan P, Kim, Cecilia, Gidaya, Nicole B, Lindquist, Ingrid, Hutman, Ted, Sigman, Marian, Kustanovich, Vlad, Lajonchere, Clara M, Singleton, Andrew, Kim, Junhyong, Wassink, Thomas H, McMahon, William M, Owley, Thomas, Sweeney, John A, Coon, Hilary, Nurnberger, John I, Li, Mingyao, Cantor, Rita M, Minshew, Nancy J, Sutcliffe, James S, Cook, Edwin H, Dawson, Geraldine, Buxbaum, Joseph D, Grant, Struan F A, Schellenberg, Gerard D, Geschwind, Daniel H, Hakonarson, Hakon

Volltext