MAPPIN: a method for annotating, predicting pathogenicity and mode of inheritance for nonsynonymous variants

Por Gosalia, Nehal, Economides, Aris N., Dewey, Frederick E., Balasubramanian, Suganthi
Publicado no Nucleic Acids Res (2017)

DNA sequencing: Clinical applications of new DNA sequencing technologies

Por Dewey, Frederick E., Pan, Stephen, Wheeler, Matthew T, Quake, Stephen R., Ashley, Euan A.
Publicado em 2012

Added Value of a Resting ECG Neural Network That Predicts Cardiovascular Mortality

Por Perez, Marco V., Dewey, Frederick E., Tan, Swee Y., Myers, Jonathan, Froelicher, Victor F.
Publicado no Ann Noninvasive Electrocardiol (2009)

Hemoglobin Levels Predict Exercise Performance, ST‐Segment Depression, and Outcome in Patients Referred for Routine Exercise Treadmill Testing

Por Lipinski, Michael J., Dewey, Frederick E., Biondi‐Zoccai, Giuseppe G., Abbate, Antonio, Vetrovec, George W., Froelicher, Victor F.
Publicado no Clin Cardiol (2009)

Gene Coexpression Network Topology of Cardiac Development, Hypertrophy, and Failure

Por Dewey, Frederick E., Perez, Marco V., Wheeler, Matthew T., Watt, Clifton, Spin, Joshua, Langfelder, Peter, Horvath, Stephen, Hannenhalli, Sridhar, Cappola, Thomas P., Ashley, Euan A.
Publicado em 2010

CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data

Por Packer, Jonathan S., Maxwell, Evan K., O’Dushlaine, Colm, Lopez, Alexander E., Dewey, Frederick E., Chernomorsky, Rostislav, Baras, Aris, Overton, John D., Habegger, Lukas, Reid, Jeffrey G.
Publicado no Bioinformatics (2016)

Rare variants in drug target genes contributing to complex diseases, phenome-wide

Por Verma, Shefali Setia, Josyula, Navya, Verma, Anurag, Zhang, Xinyuan, Veturi, Yogasudha, Dewey, Frederick E., Hartzel, Dustin N., Lavage, Daniel R., Leader, Joe, Ritchie, Marylyn D., Pendergrass, Sarah A.
Publicado no Sci Rep (2018)

Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

Por Verma, Shefali Setia, Josyula, Navya, Verma, Anurag, Zhang, Xinyuan, Veturi, Yogasudha, Dewey, Frederick E., Hartzel, Dustin N., Lavage, Daniel R., Leader, Joe, Ritchie, Marylyn D., Pendergrass, Sarah A.
Publicado no Sci Rep (2018)

Molecular Diagnosis of Long-QT syndrome at 10 Days of Life by Rapid Whole Genome Sequencing

Por Priest, James R., Ceresnak, Scott R., Dewey, Frederick E., Malloy-Walton, Lindsey E., Dunn, Kyla, Grove, Megan E., Perez, Marco V., Maeda, Katsuhide, Dubin, Anne M., Ashley, Euan A.
Publicado no Heart Rhythm (2014)

Performance comparison of whole-genome sequencing platforms

Por Lam, Hugo Y K, Clark, Michael J, Chen, Rui, Chen, Rong, Natsoulis, Georges, O’Huallachain, Maeve, Dewey, Frederick E, Habegger, Lukas, Ashley, Euan A, Gerstein, Mark B, Butte, Atul J, Ji, Hanlee P, Snyder, Michael
Publicado em 2011

Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data

Por Dewey, Frederick E., Grove, Megan E., Priest, James R., Waggott, Daryl, Batra, Prag, Miller, Clint L., Wheeler, Matthew, Zia, Amin, Pan, Cuiping, Karzcewski, Konrad J., Miyake, Christina, Whirl-Carrillo, Michelle, Klein, Teri E., Datta, Somalee, Altman, Russ B., Snyder, Michael, Quertermous, Thomas, Ashley, Euan A.
Publicado no PLoS Genet (2015)

INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES

Por Verma, Anurag, Leader, Joseph B., Verma, Shefali S., Frase, Alex, Wallace, John, Dudek, Scott, Lavage, Daniel R., Van Hout, Cristopher V., Dewey, Frederick E., Penn, John, Lopez, Alex, Overton, John D., Carey, David J., Ledbetter, David H., Kirchner, H. Lester, Ritchie, Marylyn D., Pendergrass, Sarah A.
Publicado no Pac Symp Biocomput (2016)

Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation

Por Homburger, Julian R., Green, Eric M., Caleshu, Colleen, Sunitha, Margaret S., Taylor, Rebecca E., Ruppel, Kathleen M., Metpally, Raghu Prasad Rao, Colan, Steven D., Michels, Michelle, Day, Sharlene M., Olivotto, Iacopo, Bustamante, Carlos D., Dewey, Frederick E., Ho, Carolyn Y., Spudich, James A., Ashley, Euan A.
Publicado no Proc Natl Acad Sci U S A (2016)

Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease

Por Zhu, Na, Welch, Carrie L., Wang, Jiayao, Allen, Philip M., Gonzaga-Jauregui, Claudia, Ma, Lijiang, King, Alejandra K., Krishnan, Usha, Rosenzweig, Erika B., Ivy, D. Dunbar, Austin, Eric D., Hamid, Rizwan, Pauciulo, Michael W., Lutz, Katie A., Nichols, William C., Reid, Jeffrey G., Overton, John D., Baras, Aris, Dewey, Frederick E., Shen, Yufeng, Chung, Wendy K.
Publicado no Genome Med (2018)

Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease

Por Peloso, Gina M., Nomura, Akihiro, Khera, Amit V., Chaffin, Mark, Won, Hong-Hee, Ardissino, Diego, Danesh, John, Schunkert, Heribert, Wilson, James G., Samani, Nilesh, Erdmann, Jeanette, McPherson, Ruth, Watkins, Hugh, Saleheen, Danish, McCarthy, Shane, Teslovich, Tanya M., Leader, Joseph B., Lester Kirchner, H., Marrugat, Jaume, Nohara, Atsushi, Kawashiri, Masa-aki, Tada, Hayato, Dewey, Frederick E., Carey, David J., Baras, Aris, Kathiresan, Sekar
Publicado no Circ Cardiovasc Genet (2019)

Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

Por Dewey, Frederick E., Gusarova, Viktoria, O’Dushlaine, Colm, Gottesman, Omri, Trejos, Jesus, Hunt, Charleen, Van Hout, Cristopher V., Habegger, Lukas, Buckler, David, Lai, Ka-Man V., Leader, Joseph B., Murray, Michael F., Ritchie, Marylyn D., Kirchner, H. Lester, Ledbetter, David H., Penn, John, Lopez, Alexander, Borecki, Ingrid B., Overton, John D., Reid, Jeffrey G., Carey, David J., Murphy, Andrew J., Yancopoulos, George D., Baras, Aris, Gromada, Jesper, Shuldiner, Alan R.
Publicado no N Engl J Med (2016)

Clinical Interpretation and Implications of Whole-Genome Sequencing

Por Dewey, Frederick E., Grove, Megan E., Pan, Cuiping, Goldstein, Benjamin A., Bernstein, Jonathan A., Chaib, Hassan, Merker, Jason D., Goldfeder, Rachel L., Enns, Gregory M., David, Sean P., Pakdaman, Neda, Ormond, Kelly E., Caleshu, Colleen, Kingham, Kerry, Klein, Teri E., Whirl-Carrillo, Michelle, Sakamoto, Kenneth, Wheeler, Matthew T., Butte, Atul J., Ford, James M., Boxer, Linda, Ioannidis, John P. A., Yeung, Alan C., Altman, Russ B., Assimes, Themistocles L., Snyder, Michael, Ashley, Euan A., Quertermous, Thomas
Publicado em 2014

Early somatic mosaicism is a rare cause of long-QT syndrome

Por Priest, James Rush, Gawad, Charles, Kahlig, Kristopher M., Yu, Joseph K., O’Hara, Thomas, Boyle, Patrick M., Rajamani, Sridharan, Clark, Michael J., Garcia, Sarah T. K., Ceresnak, Scott, Harris, Jason, Boyle, Sean, Dewey, Frederick E., Malloy-Walton, Lindsey, Dunn, Kyla, Grove, Megan, Perez, Marco V., Neff, Norma F., Chen, Richard, Maeda, Katsuhide, Dubin, Anne, Belardinelli, Luiz, West, John, Antolik, Christian, Macaya, Daniela, Quertermous, Thomas, Trayanova, Natalia A., Quake, Stephen R., Ashley, Euan A.
Publicado no Proc Natl Acad Sci U S A (2016)

Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes

Por Staples, Jeffrey, Maxwell, Evan K., Gosalia, Nehal, Gonzaga-Jauregui, Claudia, Snyder, Christopher, Hawes, Alicia, Penn, John, Ulloa, Ricardo, Bai, Xiaodong, Lopez, Alexander E., Van Hout, Cristopher V., O’Dushlaine, Colm, Teslovich, Tanya M., McCarthy, Shane E., Balasubramanian, Suganthi, Kirchner, H. Lester, Leader, Joseph B., Murray, Michael F., Ledbetter, David H., Shuldiner, Alan R., Yancoupolos, George D., Dewey, Frederick E., Carey, David J., Overton, John D., Baras, Aris, Habegger, Lukas, Reid, Jeffrey G.
Publicado no Am J Hum Genet (2018)

Clinical evaluation incorporating a personal genome

Por Ashley, Euan A., Butte, Atul J., Wheeler, Matthew T., Chen, Rong, Klein, Teri E., Dewey, Frederick E., Dudley, Joel T., Ormond, Kelly E., Pavlovic, Aleksandra, Hudgins, Louanne, Gong, Li, Hodges, Laura M., Berlin, Dorit S., Thorn, Caroline F., Sangkuhl, Katrin, Hebert, Joan M., Woon, Mark, Sagreiya, Hersh, Whaley, Ryan, Morgan, Alexander A., Pushkarev, Dmitry, Neff, Norma F, Knowles, Joshua W., Chou, Mike, Thakuria, Joseph, Rosenbaum, Abraham, Zaranek, Alexander Wait, Church, George, Greely, Henry T., Quake, Stephen R., Altman, Russ B.
Publicado em 2010