Multi-omic integrated networks connect DNA methylation and miRNA with skeletal muscle plasticity to chronic exercise in Type 2 diabetic obesity
Rowlands, David S, Page, Rachel A, Sukala, William R, Giri, Mamta, Ghimbovschi, Svetlana D, Hayat, Irum, Cheema, Birinder S, Lys, Isabelle, Leikis, Murray, Sheard, Phillip W, Wakefield, St John, Breier, Bernhard, Hathout, Yetrib, Brown, Kristy, Marathi, Ramya, Orkunoglu-Suer, Funda E, Devaney, Joseph M, Leiken, Benjamin, Many, Gina, Krebs, Jeremy, Hopkins, Will G, Hoffman, Eric P
Published in Physiological genomics (15.10.2014)
Published in Physiological genomics (15.10.2014)
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Kinase insert domain receptor/vascular endothelial growth factor receptor 2 (KDR) genetic variation is associated with ovarian hyperstimulation syndrome
O'Brien, Travis J, Harralson, Arthur F, Tran, Tuyen, Gindoff, Ian, Orkunoglu-Suer, Funda E, Frankfurter, David, Gindoff, Paul
Published in Reproductive biology and endocrinology (09.05.2014)
Published in Reproductive biology and endocrinology (09.05.2014)
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Lessons learned from expanded reproductive carrier screening in self‐reported Ashkenazi, Sephardi, and Mizrahi Jewish patients
Akler, Gidon, Birch, Ashley H., Schreiber‐Agus, Nicole, Cai, Xiaoqiang, Cai, Guiqing, Shi, Lisong, Yu, Chunli, Larmore, Anastasia M., Mendiratta‐Vij, Geetu, Elkhoury, Lama, Dillon, Mitchell W., Zhu, Jun, Mclellan, Andrew S., Suer, Funda E., Webb, Bryn D., Schadt, Eric E., Kornreich, Ruth, Edelmann, Lisa
Published in Molecular genetics & genomic medicine (01.02.2020)
Published in Molecular genetics & genomic medicine (01.02.2020)
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MC4R Variant Is Associated With BMI but Not Response to Resistance Training in Young Females
Orkunoglu‐Suer, Funda E., Harmon, Brennan T., Gordish‐Dressman, Heather, Clarkson, Priscilla M., Thompson, Paul D., Angelopoulos, Theodore J., Gordon, Paul M., Hubal, Monica J., Moyna, Niall M., Pescatello, Linda S., Visich, Paul S., Zoeller, Robert F., Hoffman, Eric P., Devaney, Joseph M.
Published in Obesity (Silver Spring, Md.) (01.03.2011)
Published in Obesity (Silver Spring, Md.) (01.03.2011)
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Differences in fat and muscle mass associated with a functional human polymorphism in a post-transcriptional BMP2 gene regulatory element
Devaney, Joseph M., Tosi, Laura L., Fritz, David T., Gordish-Dressman, Heather A., Jiang, Shan, Orkunoglu-Suer, Funda E., Gordon, Andrew H., Harmon, Brennan T., Thompson, Paul D., Clarkson, Priscilla M., Angelopoulos, Theodore J., Gordon, Paul M., Moyna, Niall M., Pescatello, Linda S., Visich, Paul S., Zoeller, Robert F., Brandoli, Cinzia, Hoffman, Eric P., Rogers, Melissa B.
Published in Journal of cellular biochemistry (15.08.2009)
Published in Journal of cellular biochemistry (15.08.2009)
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CCL2 and CCR2 variants are associated with skeletal muscle strength and change in strength with resistance training
HARMON, Brennan T, FUNDA ORKUNOGLU-SUER, E, PESCATELLO, Linda S, VISICH, Paul S, ZOELLER, Robert F, HUBAL, Monica J, TOSI, Laura L, HOFFMAN, Eric P, DEVANEY, Joseph M, ADHAM, Kasra, LARKIN, Justin S, GORDISH-DRESSMAN, Heather, CLARKSON, Priscilla M, THOMPSON, Paul D, ANGELOPOULOS, Theodore J, GORDON, Paul M, MOYNA, Niall M
Published in Journal of applied physiology (1985) (01.12.2010)
Published in Journal of applied physiology (1985) (01.12.2010)
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INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
Orkunoglu-Suer, Funda E, Gordish-Dressman, Heather, Clarkson, Priscilla M, Thompson, Paul D, Angelopoulos, Theodore J, Gordon, Paul M, Moyna, Niall M, Pescatello, Linda S, Visich, Paul S, Zoeller, Robert F, Harmon, Brennan, Seip, Richard L, Hoffman, Eric P, Devaney, Joseph M
Published in BMC medical genetics (23.12.2008)
Published in BMC medical genetics (23.12.2008)
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The 1p13.3 LDL (C)-Associated Locus Shows Large Effect Sizes in Young Populations
Devaney, Joseph M, Thompson, Paul D, Visich, Paul S, Saltarelli, William A, Gordon, Paul M, Orkunoglu-Suer, E Funda, Gordish-Dressman, Heather, Harmon, Brennan T, Bradbury, Margaret K, Panchapakesan, Karuna, Khianey, Rahul, Hubal, Monica J, Clarkson, Priscilla M, Pescatello, Linda S, Zoeller, Robert F, Moyna, Niall M, Angelopoulos, Theodore J, Kraus, William E, Hoffman, Eric P
Published in Pediatric research (01.06.2011)
Published in Pediatric research (01.06.2011)
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SLC30A8 nonsynonymous variant is associated with recovery following exercise and skeletal muscle size and strength
Sprouse, Courtney, Gordish-Dressman, Heather, Orkunoglu-Suer, E Funda, Lipof, Jason S, Moeckel-Cole, Stephanie, Patel, Ronak R, Adham, Kasra, Larkin, Justin S, Hubal, Monica J, Kearns, Amy K, Clarkson, Priscilla M, Thompson, Paul D, Angelopoulos, Theodore J, Gordon, Paul M, Moyna, Niall M, Pescatello, Linda S, Visich, Paul S, Zoeller, Robert F, Hoffman, Eric P, Tosi, Laura L, Devaney, Joseph M
Published in Diabetes (New York, N.Y.) (01.01.2014)
Published in Diabetes (New York, N.Y.) (01.01.2014)
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Homozygous GDF1 mutation causing congenital heart defects in Ashkenazi Jewish families
Swaroop, Pooja, Beltran, Carlos Mares, Suer, Funda, Iverson, Ayuko, Mehta, Lakshmi
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs
DiStefano, Marina T., Hemphill, Sarah E., Oza, Andrea M., Siegert, Rebecca K., Grant, Andrew R., Hughes, Madeline Y., Cushman, Brandon J., Azaiez, Hela, Booth, Kevin T., Chapin, Alex, Duzkale, Hatice, Matsunaga, Tatsuo, Shen, Jun, Zhang, Wenying, Kenna, Margaret, Schimmenti, Lisa A., Tekin, Mustafa, Rehm, Heidi L., Tayoun, Ahmad N. Abou, Amr, Sami S.
Published in Genetics in medicine (01.10.2019)
Published in Genetics in medicine (01.10.2019)
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Response to Comment on Sprouse et al. SLC30A8 nonsynonymous variant is associated with recovery following exercise and skeletal muscle size and strength. Diabetes 2014;63:363-368
Sprouse, Courtney, Gordish-Dressman, Heather, Orkunoglu-Suer, E Funda, Lipof, Jason S, Moeckel-Cole, Stephanie, Patel, Ronak R, Adham, Kasra, Larkin, Justin S, Hubal, Monica J, Kearns, Amy K, Clarkson, Priscilla M, Thompson, Paul D, Angelopoulos, Theodore J, Gordon, Paul M, Moyna, Niall M, Pescatello, Linda S, Visich, Paul S, Zoeller, Robert F, Hoffman, Eric P, Tosi, Laura L, Devaney, Joseph M
Published in Diabetes (New York, N.Y.) (01.05.2014)
Published in Diabetes (New York, N.Y.) (01.05.2014)
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eP109: Clinical efficacy of next-generation sequencing panels for hearing loss diagnostics
Suer, Funda, Mazur, Zehra, Zhang, Ying, Cody, Neal, Fox, Rebecca, Shaw, Jay, Shi, Lisong, Shrivastava, Vibha, Mendiratta, Geetu, Newman, Scott, Kasarskis, Andrew, Zhang, Kejian, Zimmerman, Rebekah, Kornreich, Ruth, Schadt, Eric E., Edelmann, Lisa, Dincer, Aslihan
Published in Genetics in medicine (01.03.2022)
Published in Genetics in medicine (01.03.2022)
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Targeted single molecule sequencing methodology for ovarian hyperstimulation syndrome
Orkunoglu-Suer, Funda, Harralson, Arthur F, Frankfurter, David, Gindoff, Paul, O'Brien, Travis J
Published in BMC genomics (03.04.2015)
Published in BMC genomics (03.04.2015)
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Abstract 4999: Genome-wide methylation array of human prostate tissues using illumina infunium 450K bead chip reveals distinct DNA methylation signatures with potential as clinical predictors
Kwabi-Addo, Bernard, Wang, Songping, Lee, Norman H., Ittmann, Michael, Suer, Funda, Devaney, Joseph
Published in Cancer research (Chicago, Ill.) (15.04.2012)
Published in Cancer research (Chicago, Ill.) (15.04.2012)
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ClinGen expert clinical validity curation of 164 hearing lossgene–disease pairs
DiStefano, Marina T, Hemphill, Sarah E, Oza, Andrea M, Siegert, Rebecca K, Grant, Andrew R, Hughes, Madeline Y, Cushman, Brandon J, Azaiez Hela, Booth, Kevin T, Chapin, Alex, Duzkale Hatice, Matsunaga Tatsuo, Shen, Jun, Zhang, Wenying, Kenna, Margaret, Schimmenti, Lisa A, Tekin Mustafa, Rehm, Heidi L, Tayoun Ahmad N Abou, Amr, Sami S, Abdelhak Sonia, Alexander, John, Avraham, Karen, Bhatia Neha, Bai Donglin, Boczek Nicole, Brownstein Zippora, Burt, Rachel, Bylstra Yasmin, del Castillo Ignacio, Choi, Byung Yoon, Downie, Lilian, Friedman, Thomas, Giersch, Anne, Goh Jasmine, Greinwald, John, Griffith, Andrew J, Hernandez, Amy, Holt, Jeffrey, Hosoya Makoto, Ying Lim Jiin, Jain Kanika, Un-Kyung, Kim, Kremer Hannie, Krantz, Ian, Leal, Suzanne, Lewis, Morag, Liu Xue Zhong, Low, Wendy, Lu, Yu, Luo Minjie, Masmoudi Saber, Ming Tan Yuen, Moreno-Pelayo, Miguel Angel, Morín Matías, Morton, Cynthia, Murray, Jaclyn, Mutai Hideki, Kiyomitsu, Nara, Pandya Arti, Pei-Rong, Sylvia Kam, Smith Richard J H, Jamuar Saumya Shekhar, Suer Funda Elif, Usami Shin-Ichi, Van Camp Guy, Yamazawa Kazuki, Hui-Jun, Yuan, Black-Zeigelbein, Elizabeth, Zhang Keijan
Published in Genetics in medicine (01.10.2019)
Published in Genetics in medicine (01.10.2019)
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