GENETIC AND EPIGENETIC CAUSES OF OBESITY

Por Thaker, Vidhu V.
Publicado no Adolesc Med State Art Rev (2017)

OR22-04 Relationship of TSH Levels with the Components of Metabolic Syndrome in a Nationally Representative Population of Youth in the United States

Por Chen, Xinlei, Deng, Shuliang, Thaker, Vidhu V
Publicado no J Endocr Soc (2020)

Clinical Course of Nonfunctional Pituitary Microadenoma in Children: A Single-Center Experience

Por Thaker, Vidhu V, Lage, Adrianne E, Kumari, Garima, Silvera, V Michelle, Cohen, Laurie E
Publicado no J Clin Endocrinol Metab (2019)

Effect of TSH on Non-Alcoholic Fatty Liver Disease (NAFLD) independent of obesity in children of predominantly Hispanic/Latino ancestry by causal mediation analysis

Por Nichols, Presley H., Pan, Yue, May, Benjamin, Pavlicova, Martina, Rausch, John C., Mencin, Ali A., Thaker, Vidhu V.
Publicado no PLoS One (2020)

Impact of an electronic template on documentation of obesity in a primary care clinic

Por Thaker, Vidhu V., Lee, Felix, Bottino, Clement J., Perry, Cassandra L., Holm, Ingrid A., Hirschhorn, Joel N., Osganian, Stavroula K.
Publicado no Clin Pediatr (Phila) (2015)

Psychosocial, behavioral and clinical correlates of children with overweight and obesity

Por Thaker, Vidhu V., Osganian, Stavroula K., deFerranti, Sarah D., Sonneville, Kendrin R., Cheng, Jennifer K., Feldman, Henry A., Richmond, Tracy K.
Publicado no BMC Pediatr (2020)

Hypothyroidism in Infants With Congenital Heart Disease Exposed to Excess Iodine

Por Thaker, Vidhu V., Galler, Marjorie F., Marshall, Audrey C., Almodovar, Melvin C., Hsu, Ho-Wen, Addis, Christopher J., Feldman, Henry A., Brown, Rosalind S., Levine, Bat-Sheva
Publicado no J Endocr Soc (2017)

OR33-07 ARNT2: A Potential Novel Candidate Gene for Monogenic Obesity in Humans

Por Thaker, Vidhu V, Seaby, Eleanor G, Genetti, Casie, Sutherland, Jacob, Ianello, Grazia, Rajabi, Farrah, Schreiber, John M, Doege, Claudia A, Turer, Emre E, Hirschhorn, Joel N, Agrawal, Pankaj B
Publicado no J Endocr Soc (2020)

OR33-06 Potential Role of Mutations in TBX3 in Human Weight Regulation

Por Xu, Yanjun, De Rosa, Maria Caterina, Quarta, Carmelo, Fisette, Alexander, Rausch, Richard, Fleischman, Amy Debra, Tschöp, Matthias H, García-Cáceres, Cristina, Hirschhorn, Joel N, Doege, Claudia A, Thaker, Vidhu V
Publicado no J Endocr Soc (2020)

Whole Exome Sequencing Identifies RAI1 Mutation in a Morbidly Obese Child Diagnosed With ROHHAD Syndrome

Por Thaker, Vidhu V., Esteves, Kristyn M., Towne, Meghan C., Brownstein, Catherine A., James, Philip M., Crowley, Laura, Hirschhorn, Joel N., Elsea, Sarah H., Beggs, Alan H., Picker, Jonathan, Agrawal, Pankaj B.
Publicado no J Clin Endocrinol Metab (2015)

Characterization of Rare Variants in MC4R in African American and Latino Children With Severe Early-Onset Obesity

Por De Rosa, Maria Caterina, Chesi, Alessandra, McCormack, Shana, Zhou, Justin, Weaver, Benjamin, McDonald, Molly, Christensen, Sinead, Liimatta, Kalle, Rosenbaum, Michael, Hakonarson, Hakon, Doege, Claudia A, Grant, Struan F A, Hirschhorn, Joel N, Thaker, Vidhu V
Publicado no J Clin Endocrinol Metab (2019)

Suboptimal Clinical Documentation in Young Children with Severe Obesity at Tertiary Care Centers

Por Brady, Cassandra C., Thaker, Vidhu V., Lingren, Todd, Woo, Jessica G., Kennebeck, Stephanie S., Namjou-Khales, Bahram, Roach, Ashton, Bickel, Jonathan P., Patibandla, Nandan, Savova, Guergana K., Solti, Imre, Holm, Ingrid A., Harley, John B., Kohane, Isaac S., Crimmins, Nancy A.
Publicado no Int J Pediatr (2016)