i-Soc: An Info-Sociological Approach to Structural–Agent Causal Symmetry

Por Shing-Chung Jonathan Yam
Publicado em 2020-04-01

Traumatic Ventricular Septal Defect: Characterization with ECG-Gated Cardiac Computed Tomography Angiography (CTA)

Por Rojas, Carlos A., Cruite, Dana M., Chung, Jonathan H.
Publicado em 2012

Secondary Pulmonary Alveolar Proteinosis: A Confusing and Potentially Serious Complication of Hematological Malignancy (Original research)

Por Chung, Jonathan H., Pipavath, Sudhakar J., Myerson, David H., Godwin, J. David
Publicado em 2009

Exploring Visual Selective Attention towards Novel Stimuli in Alzheimer's Disease Patients

Por Chau, Sarah A., Herrmann, Nathan, Eizenman, Moshe, Chung, Jonathan, Lanctôt, Krista L.
Publicado no Dement Geriatr Cogn Dis Extra (2015)

Whole genome sequencing and integrative genomic analysis approach on two 22q11.2 deletion syndrome family trios for genotype to phenotype correlations

Por Chung, Jonathan H., Cai, Jinlu, Suskin, Barrie G., Zhang, Zhengdong, Coleman, Karlene, Morrow, Bernice E.
Publicado no Hum Mutat (2015)

Lymphomatoid Granulomatosis: CT and FDG-PET Findings

Por Chung, Jonathan H., Wu, Carol C., Gilman, Matthew D., Palmer, Edwin L., Hasserjian, Robert P., Shepard, Jo-Anne O.
Publicado em 2011

Autoimmune Hypothyroidism As a Predictor of Mortality in Chronic Hypersensitivity Pneumonitis

Por Adegunsoye, Ayodeji, Oldham, Justin M., Husain, Aliya N., Chen, Lena, Hsu, Scully, Montner, Steven, Chung, Jonathan H., Vij, Rekha, Noth, Imre, Strek, Mary E.
Publicado no Front Med (Lausanne) (2017)

Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation

Por Racedo, Silvia E., McDonald-McGinn, Donna M., Chung, Jonathan H., Goldmuntz, Elizabeth, Zackai, Elaine, Emanuel, Beverly S., Zhou, Bin, Funke, Birgit, Morrow, Bernice E.
Publicado no Am J Hum Genet (2015)

Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome

Por Guo, Tingwei, Chung, Jonathan H., Wang, Tao, McDonald-McGinn, Donna M., Kates, Wendy R., Hawuła, Wanda, Coleman, Karlene, Zackai, Elaine, Emanuel, Beverly S., Morrow, Bernice E.
Publicado no Am J Hum Genet (2015)

Azathioprine Response in Patients with Fibrotic Connective Tissue Disease-associated Interstitial Lung Disease

Por Oldham, Justin M., Lee, Cathryn, Valenzi, Eleanor, Witt, Leah J., Adegunsoye, Ayodeji, Hsu, Scully, Chen, Lena, Montner, Steven, Chung, Jonathan H., Noth, Imre, Vij, Rekha, Strek, Mary E.
Publicado no Respir Med (2016)

Interstitial Pneumonia With Autoimmune Features: Value of Histopathology

Por Adegunsoye, Ayodeji, Oldham, Justin M., Valenzi, Eleanor, Lee, Cathryn, Witt, Leah J., Chen, Lena, Montner, Steven, Chung, Jonathan H., Noth, Imre, Vij, Rekha, Strek, Mary E., Husain, Aliya N.
Publicado no Arch Pathol Lab Med (2017)

Cost-Effectiveness of Follow-Up of Pulmonary Nodules Incidentally Detected on Cardiac CT Angiography in Patients with Suspected Coronary Artery Disease

Por Goehler, Alexander, McMahon, Pamela M, Lumish, Heidi S, Wu, Carol, Munshi, Vidit, Gilmore, Michael, Chung, Jonathan H, Ghoshhajra, Brian B., Mark, Daniel, Truong, Quynh A, Gazelle, G Scott, Hoffmann, Udo
Publicado em 2014

CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism

Por Chung, Jonathan H., Peljto, Anna L., Chawla, Ashish, Talbert, Janet L., McKean, David F., Rho, Byung-Hak, Fingerlin, Tasha E., Schwarz, Marvin I., Schwartz, David A., Lynch, David A.
Publicado no Chest (2016)

Characterisation of patients with interstitial pneumonia with autoimmune features

Por Oldham, Justin M., Adegunsoye, Ayodeji, Valenzi, Eleanor, Lee, Cathryn, Witt, Leah, Chen, Lena, Husain, Aliya N., Montner, Steven, Chung, Jonathan H., Cottin, Vincent, Fischer, Aryeh, Noth, Imre, Vij, Rekha, Strek, Mary E.
Publicado no Eur Respir J (2016)

CT Scan Findings of Probable Usual Interstitial Pneumonitis Have a High Predictive Value for Histologic Usual Interstitial Pneumonitis

Por Chung, Jonathan H., Chawla, Ashish, Peljto, Anna L., Cool, Carlyne D., Groshong, Steve D., Talbert, Janet L., McKean, David F., Brown, Kevin K., Fingerlin, Tasha E., Schwarz, Marvin I., Schwartz, David A., Lynch, David A.
Publicado no Chest (2015)

Outcomes of immunosuppressive therapy in chronic hypersensitivity pneumonitis

Por Adegunsoye, Ayodeji, Oldham, Justin M., Fernández Pérez, Evans R., Hamblin, Mark, Patel, Nina, Tener, Mitchell, Bhanot, Deepa, Robinson, Lacey, Bullick, Sam, Chen, Lena, Hsu, Scully, Churpek, Matthew, Hedeker, Donald, Montner, Steven, Chung, Jonathan H., Husain, Aliya N., Noth, Imre, Strek, Mary E., Vij, Rekha
Publicado no ERJ Open Res (2017)

Coronary Plaque Characterization in Psoriasis Reveals High Risk Features Which Improve Following Treatment in a Prospective Observational Study

Por Lerman, Joseph B, Joshi, Aditya A, Chaturvedi, Abhishek, Aberra, Tsion M, Dey, Amit K, Rodante, Justin A, Salahuddin, Taufiq, Chung, Jonathan H, Rana, Anshuma, Teague, Heather L, Wu, Jashin J, Playford, Martin P, Lockshin, Benjamin A, Chen, Marcus Y, Sandfort, Veit, Bluemke, David A, Mehta, Nehal N
Publicado no Circulation (2017)

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio- facial/DiGeorge/22q11.2 deletion syndrome patients

Por Guo, Tingwei, McGinn, Donna McDonald, Blonska, Anna, Shanske, Alan, Bassett, Anne, Chow, Eva, Bowser, Mark, Sheridan, Molly, Beemer, Frits, Devriendt, Koen, Swillen, Ann, Breckpot, Jeroen, Digilio, M. Cristina, Marino, Bruno, Dallapiccola, Bruno, Carpenter, Courtney, Zheng, Xin, Johnson, Jacob, Chung, Jonathan, Higgins, Anne Marie, Philip, Nicole, Simon, Tony J., Coleman, Karlene, Heine-Suner, Damian, Rosell, Jordi, Kates, Wendy, Devoto, Marcella, Goldmuntz, Elizabeth, Zackai, Elaine, Wang, Tao, Shprintzen, Robert, Emanuel, Beverly, Morrow, Bernice
Publicado em 2011

Overt Cleft Palate Phenotype and TBX1 Genotype Correlations in Velo-cardio-facial/DiGeorge/22q11.2 Deletion Syndrome Patients

Por Herman, Sean B., Guo, Tingwei, McGinn, Donna M. McDonald, Blonska, Anna, Shanske, Alan L., Bassett, Anne S., Chow, Eva WC, Bowser, Mark, Sheridan, Molly, Beemer, Frits, Devriendt, Koen, Swillen, Ann, Breckpot, Jeroen, Digilio, M. Cristina, Marino, Bruno, Dallapiccola, Bruno, Carpenter, Courtney, Zheng, Xin, Johnson, Jacob, Chung, Jonathan, Higgins, Anne Marie, Philip, Nicole, Simon, Tony, Coleman, Karlene, Heine-Suner, Damian, Rosell, Jordi, Kates, Wendy, Devoto, Marcella, Zackai, Elaine, Wang, Tao, Shprintzen, Robert, Emanuel, Beverly S., Morrow, Bernice E.
Publicado em 2012

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado no Circ Cardiovasc Genet (2017)