DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and Palate

por Young, Juan I., Slifer, Susan, Hecht, Jacqueline T., Blanton, Susan H.
Publicado 2021

Targeted sequencing of linkage region in Dominican families implicates PRIMA1 and the SPATA7-PTPN21-ZC3H14-EML5-TTC8 locus in carotid-intima media thickness and atherosclerotic eve...

por Wang, Liyong, Dueker, Nicole, Beecham, Ashley, Blanton, Susan H., Sacco, Ralph L., Rundek, Tatjana
Publicado 2019

Rare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families

por Dueker, Nicole D., Beecham, Ashley, Wang, Liyong, Blanton, Susan H., Guo, Shengru, Rundek, Tatjana, Sacco, Ralph L.
Publicado 2016

Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families

por Dueker, Nicole D., Beecham, Ashley, Wang, Liyong, Dong, Chuanhui, Sacco, Ralph L., Blanton, Susan H., Rundek, Tatjana
Publicado 2022

Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis

por Wang, Liyong, Beecham, Ashley, Di Tullio, Marco R, Slifer, Susan, Blanton, Susan H, Rundek, Tatjana, Sacco, Ralph L
Publicado 2009

Sequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families

por Dueker, Nicole D., Guo, Shengru, Beecham, Ashley, Wang, Liyong, Blanton, Susan H., Di Tullio, Marco R., Rundek, Tatjana, Sacco, Ralph L.
Publicado 2017

Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy

por de Joya, Evan M., Colbert, Brett M., Tang, Pei-Ciao, Lam, Byron L., Yang, Jun, Blanton, Susan H., Dykxhoorn, Derek M., Liu, Xuezhong
Publicado 2021

A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes

por Della-Morte, David, Beecham, Ashley, Rundek, Tatjana, Wang, Liyong, McClendon, Mark S, Slifer, Susan, Blanton, Susan H, Di Tullio, Marco R, Sacco, Ralph L
Publicado 2011

Association of the Sirtuin and Mitochondrial Uncoupling Protein Genes with Carotid Plaque

por Dong, Chuanhui, Della-Morte, David, Wang, Liyong, Cabral, Digna, Beecham, Ashley, McClendon, Mark S., Luca, Corneliu C., Blanton, Susan H., Sacco, Ralph L., Rundek, Tatjana
Publicado 2011

Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family

por Cvjetkovic, Nevena, Maili, Lorena, Weymouth, Katelyn S, Hashmi, S Shahrukh, Mulliken, John B, Topczewski, Jacek, Letra, Ariadne, Yuan, Qiuping, Blanton, Susan H, Swindell, Eric C, Hecht, Jacqueline T
Publicado 2015

Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensities

por Beecham, Ashley, Dong, Chuanhui, Wright, Clinton B., Dueker, Nicole, Brickman, Adam M., Wang, Liyong, DeCarli, Charles, Blanton, Susan H., Rundek, Tatjana, Mayeux, Richard, Sacco, Ralph L.
Publicado 2017

Genetics and the Individualized Therapy of Vestibular Disorders

por Mei, Christine, Dong, Hongsong, Nisenbaum, Eric, Thielhelm, Torin, Nourbakhsh, Aida, Yan, Denise, Smeal, Molly, Lundberg, Yesha, Hoffer, Michael E., Angeli, Simon, Telischi, Fred, Nie, Guohui, Blanton, Susan H., Liu, Xuezhong
Publicado 2021

North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene

por Bowne, Sara J., Sullivan, Lori S., Wheaton, Dianna K., Locke, Kirsten G., Jones, Kaylie D., Koboldt, Daniel C., Fulton, Robert S., Wilson, Richard K., Blanton, Susan H., Birch, David G., Daiger, Stephen P.
Publicado 2016

UTILITY OF BLOOD PRESSURE GENETIC RISK SCORE IN ADMIXED HISPANIC SAMPLES

por Beecham, Ashley H., Wang, Liyong, Vasudeva, Namrata, Liu, Zhi, Dong, Chaunhui, Goldschmidt-Clermont, Pascal J., Pericak-Vance, Margaret A., Rundek, Tatjana, Seo, David, Blanton, Susan H., Sacco, Ralph L., Beecham, Gary W
Publicado 2016

Peripheral vestibular system: Age-related vestibular loss and associated deficits

por Coto, Jennifer, Alvarez, Carmen L., Cejas, Ivette, Colbert, Brett M., Levin, Bonnie E., Huppert, Joshua, Rundek, Tatjana, Balaban, Carey, Blanton, Susan H., Lee, David J., Loewenstein, David, Hoffer, Michael, Liu, Xue Zhong
Publicado 2021

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

por Yan, Denise, Xiang, Guangxin, Chai, Xingping, Qing, Jie, Shang, Haiqiong, Zou, Bing, Mittal, Rahul, Shen, Jun, Smith, Richard J. H., Fan, Yao-Shan, Blanton, Susan H., Tekin, Mustafa, Morton, Cynthia, Xing, Wanli, Cheng, Jing, Liu, Xue Zhong
Publicado 2017

COVID19: A Systematic Approach to Early Identification and Healthcare Worker Protection

por Zhao, Yu, Cui, Chong, Zhang, Kun, Liu, Jialin, Xu, Jinfu, Nisenbaum, Eric, Huang, Yixiang, Qin, Guoyou, Chen, Bing, Hoffer, Michael, Blanton, Susan H., Telischi, Fred, Hare, Joshua M., Daunert, Sylvia, Shukla, Bhavarth, Pahwa, Savita G., Jayaweera, Dushyantha T., Farmer, Paul E., del Rio, Carlos, Liu, Xuezhong, Shu, Yilai
Publicado 2020

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study

por Tao, Feifei, Beecham, Gary W., Rebelo, Adriana P., Blanton, Susan H., Moran, John J., Lopez-Anido, Camila, Svaren, John, Abreu, Lisa, Rizzo, Devon, Kirk, Callyn A., Wu, Xingyao, Feely, Shawna, Verhamme, Camiel, Saporta, Mario A., Herrmann, David N., Day, John W., Sumner, Charlotte J., Lloyd, Thomas E., Li, Jun, Yum, Sabrina W., Taroni, Franco, Baas, Frank, Choi, Byung-Ok, Pareyson, Davide, Scherer, Steven S., Reilly, Mary M., Shy, Michael E., Züchner, Stephan
Publicado 2019

Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort

por Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Horta, Oscar Diaz, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Hernandez, Fabiola Huesca, de la Luz Arenas Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa
Publicado 2015

A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

por Jang, Minwoo Wendy, Oh, Doo-Yi, Yi, Eunyoung, Liu, Xuezhong, Ling, Jie, Kim, Nayoung, Sharma, Kushal, Kim, Tai Young, Lee, Seungmin, Kim, Ah-Reum, Kim, Min Young, Kim, Min-A, Lee, Mingyu, Han, Jin-Hee, Han, Jae Joon, Park, Hye-Rim, Kim, Bong Jik, Lee, Sang-Yeon, Woo, Dong Ho, Oh, Jayoung, Oh, Soo-Jin, Du, Tingting, Koo, Ja-Won, Oh, Seung-Ha, Shin, Hyun-Woo, Seong, Moon-Woo, Lee, Kyu-Yup, Kim, Un-Kyung, Shin, Jung Bum, Sang, Shushan, Cai, Xinzhang, Mei, Lingyun, He, Chufeng, Blanton, Susan H., Chen, Zheng-Yi, Chen, Hongsheng, Liu, Xianlin, Nourbakhsh, Aida, Huang, Zaohua, Kang, Kwon-Woo, Park, Woong-Yang, Feng, Yong, Lee, C. Justin, Choi, Byung Yoon
Publicado 2021