Stigma in Practice: Barriers to Health for Fat Women

por Lee, Jennifer A., Pausé, Cat J.
Publicado 2016

Patient portals for the adolescent and young adult population: Benefits, risks and guidance for use

por Lee, Jennifer A., Holland-Hall, Cynthia
Publicado 2021

Limitations of the dorsal skinfold window chamber model in evaluating anti-angiogenic therapy during early phase of angiogenesis

por Biel, Nikolett M, Lee, Jennifer A, Sorg, Brian S, Siemann, Dietmar W
Publicado 2014

Improving Radiation Response in Glioblastoma Using ECO/siRNA Nanoparticles Targeting DNA Damage Repair

por Lee, Jennifer A., Ayat, Nadia, Sun, Zhanhu, Tofilon, Philip J., Lu, Zheng-Rong, Camphausen, Kevin
Publicado 2020

Preventing Loss of Independence through Exercise (PLIÉ): A Pilot Trial in Older Adults with Subjective Memory Decline and Mild Cognitive Impairment

por Chao, Linda L., Lee, Jennifer A., Martinez, Steven, Barlow, Cody, Chesney, Margaret A., Mehling, Wolf E., Barnes, Deborah E.
Publicado 2021

Detection of metabolic change in glioblastoma cells after radiotherapy using hyperpolarized (13)C‐MRI

por Kawai, Tatsuya, Brender, Jeffrey R., Lee, Jennifer A., Kramp, Tamalee, Kishimoto, Shun, Krishna, Murali C., Tofilon, Philip, Camphausen, Kevin A.
Publicado 2021

Associations of Telehealth Care Delivery with Pediatric Health Care Provider Well-Being

por deMayo, Richelle, Huang, Yungui, Lin, En-Ju D., Lee, Jennifer A., Heggland, Andrew, Im, Jane, Grindle, Christopher, Chandawarkar, Aarti
Publicado 2022

Telemedicine Expansion in Pediatric Gastroenterology in Response to COVID-19: Early Results of an International Physician Survey

por Miller, Steven D., Lee, Jennifer A., Murphy, Zachary, Screws, Jeremy, Berg, Elizabeth A., Picoraro, Joseph A., Gurses, Ayse P., Huang, Jeannie S.
Publicado 2020

Adaptation of an In-Person Mind-Body Movement Program for People with Cognitive Impairment or Dementia and Care Partners for Online Delivery: Feasibility, Satisfaction and Particip...

por Nicosia, Francesca M., Lee, Jennifer A., Chesney, Margaret A., Benjamin, Cynthia, Lee, Amanda N., Mehling, Wolf, Sudore, Rebecca L., Barnes, Deborah E.
Publicado 2023

Genome‐wide DNA methylation profiling confirms a case of low‐level mosaic Kabuki syndrome 1

por Montano, Carolina, Britton, Jacquelyn F., Harris, Jacqueline R., Kerkhof, Jennifer, Barnes, Benjamin T., Lee, Jennifer A., Sadikovic, Bekim, Sobreira, Nara, Fahrner, Jill A.
Publicado 2022

Reliability of blood lactate as a measure of exercise intensity in different strains of mice during forced treadmill running

por Lønbro, Simon, Wiggins, Jennifer M., Wittenborn, Thomas, Elming, Pernille Byrialsen, Rice, Lori, Pampo, Christine, Lee, Jennifer A., Siemann, Dietmar W., Horsman, Michael R.
Publicado 2019

HSD10 disease in a female: A case report and review of literature

por Upadia, Jariya, Walano, Nicolette, Noh, Grace S., Liu, Jiao, Li, Yuwen, Deputy, Stephen, Elliott, Lindsay T., Wong, Joaquin, Lee, Jennifer A., Caylor, Raymond C., Andersson, Hans C.
Publicado 2021

ClinGen’s RASopathy Expert Panel Consensus Methods for Variant Interpretation

por Gelb, Bruce D., Cavé, Hélène, Dillon, Mitchell W., Gripp, Karen W., Lee, Jennifer A., Mason-Suares, Heather, Rauen, Katherine A., Williams, Bradley, Zenker, Martin, Vincent, Lisa M.
Publicado 2018

Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort

por Ha, Kyungsoo, Anand, Priya, Lee, Jennifer A., Jones, Julie R., Kim, Chong Ae, Bertola, Debora Romeo, Labonne, Jonathan D. J., Layman, Lawrence C., Wenzel, Wolfgang, Kim, Hyung-Goo
Publicado 2016

Equity and Inclusion in Pediatric Gastroenterology Telehealth: A Study of Demographic, Socioeconomic, and Digital Disparities

por Mougey, Edward B., Judy, Wesley C., Venkatesh, Rajitha D., Berg, Elizabeth, Lee, Jennifer A., Rosen, John M., Li, B.U.K., Koster, Alex, Maiden, Kristin, Gao, Zhongcui, Franciosi, James P.
Publicado 2023

Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities

por Bend, Renee, Cohen, Lior, Carter, Melissa T., Lyons, Michael J., Niyazov, Dmitriy, Mikati, Mohamad A., Rojas, Samantha K., Person, Richard E., Si, Yue, Wentzensen, Ingrid M., Torti, Erin, Lee, Jennifer A., Boycott, Kym M., Basel-Salmon, Lina, Ferreira, Carlos R., Gonzaga-Jauregui, Claudia
Publicado 2019

Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

por Ehret, Julia K., Engels, Hartmut, Cremer, Kirsten, Becker, Jessica, Zimmermann, Johannes P., Wohlleber, Eva, Grasshoff, Ute, Rossier, Eva, Bonin, Michael, Mangold, Elisabeth, Bevot, Andrea, Schön, Stefanie, Heilmann-Heimbach, Stefanie, Dennert, Nicola, Mathieu-Dramard, Michèle, Lacaze, Elodie, Plessis, Ghislaine, de Broca, Alain, Jedraszak, Guillaume, Röthlisberger, Benno, Miny, Peter, Filges, Isabel, Dufke, Andreas, Andrieux, Joris, Lee, Jennifer A., Zink, Alexander M.
Publicado 2015

Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia

por Latham, Sharissa L., Ehmke, Nadja, Reinke, Patrick Y. A., Taft, Manuel H., Eicke, Dorothee, Reindl, Theresia, Stenzel, Werner, Lyons, Michael J., Friez, Michael J., Lee, Jennifer A., Hecker, Ramona, Frühwald, Michael C., Becker, Kerstin, Neuhann, Teresa M., Horn, Denise, Schrock, Evelin, Niehaus, Indra, Sarnow, Katharina, Grützmann, Konrad, Gawehn, Luzie, Klink, Barbara, Rump, Andreas, Chaponnier, Christine, Figueiredo, Constanca, Knöfler, Ralf, Manstein, Dietmar J., Di Donato, Nataliya
Publicado 2018

Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia

por Latham, Sharissa L., Ehmke, Nadja, Reinke, Patrick Y. A., Taft, Manuel H., Eicke, Dorothee, Reindl, Theresia, Stenzel, Werner, Lyons, Michael J., Friez, Michael J., Lee, Jennifer A., Hecker, Ramona, Frühwald, Michael C., Becker, Kerstin, Neuhann, Teresa M., Horn, Denise, Schrock, Evelin, Niehaus, Indra, Sarnow, Katharina, Grützmann, Konrad, Gawehn, Luzie, Klink, Barbara, Rump, Andreas, Chaponnier, Christine, Figueiredo, Constanca, Knöfler, Ralf, Manstein, Dietmar J., Di Donato, Nataliya
Publicado 2018

Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders

por Sadikovic, Bekim, Levy, Michael A., Kerkhof, Jennifer, Aref-Eshghi, Erfan, Schenkel, Laila, Stuart, Alan, McConkey, Haley, Henneman, Peter, Venema, Andrea, Schwartz, Charles E., Stevenson, Roger E., Skinner, Steven A., DuPont, Barbara R., Fletcher, Robin S., Balci, Tugce B., Siu, Victoria Mok, Granadillo, Jorge L., Masters, Jennefer, Kadour, Mike, Friez, Michael J., van Haelst, Mieke M., Mannens, Marcel M. A. M., Louie, Raymond J., Lee, Jennifer A., Tedder, Matthew L., Alders, Marielle
Publicado 2021