Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Phoebe Ingraham"'
Autor:
Lucilla Pizzo, Micaela Lasser, Tanzeen Yusuff, Matthew Jensen, Phoebe Ingraham, Emily Huber, Mayanglambam Dhruba Singh, Connor Monahan, Janani Iyer, Inshya Desai, Siddharth Karthikeyan, Dagny J Gould, Sneha Yennawar, Alexis T Weiner, Vijay Kumar Pounraja, Arjun Krishnan, Melissa M Rolls, Laura Anne Lowery, Santhosh Girirajan
Publikováno v:
PLoS Genetics, Vol 17, Iss 4, p e1009112 (2021)
We previously identified a deletion on chromosome 16p12.1 that is mostly inherited and associated with multiple neurodevelopmental outcomes, where severely affected probands carried an excess of rare pathogenic variants compared to mildly affected ca
Externí odkaz:
https://doaj.org/article/ea88765e5dca40999d37fc1d27f96ec3
Autor:
Callie Hlavin, Phoebe Ingraham, Tamara Byrd, Nathan Hyre, Lucine Gabriel, Nishant Agrawal, Laura Allen, Tanya Kenkre, Andrew Watson, Murat Kaynar, Bestoun Ahmed, Anita Courcoulas
Publikováno v:
JAMA Network Open. 6:e2255994
ImportanceBariatric surgery is the mainstay of treatment for medically refractory obesity; however, it is underutilized. Telemedicine affords patient cost and time savings and may increase availability and accessibility of bariatric surgery.Objective
Functional assessment of the 'two-hit' model for neurodevelopmental defects inDrosophilaandX. laevis
Autor:
Connor Monahan, Arjun Krishnan, Emily Huber, Alexis T. Weiner, Laura Anne Lowery, Matthew Jensen, Melissa M. Rolls, Lucilla Pizzo, Sneha Yennawar, Inshya Desai, Vijay Kumar Pounraja, Tanzeen Yusuff, Phoebe Ingraham, Siddharth Karthikeyan, Janani Iyer, Santhosh Girirajan, Micaela Lasser, Mayanglambam Dhruba Singh, Dagny J. Gould
We previously identified a deletion on chromosome 16p12.1 that is mostly inherited and associated with multiple neurodevelopmental outcomes, where severely affected probands carried an excess of rare pathogenic variants compared to mildly affected ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4aba6a49514567cae406c1fbb7a55d13
https://doi.org/10.1101/2020.09.14.295923
https://doi.org/10.1101/2020.09.14.295923
Autor:
Sneha Yennawar, Emily Huber, Janani Iyer, Tanzeen Yusuff, Alexis T. Weiner, Siddharth Karthikeyan, Phoebe Ingraham, Vijay Kumar Pounraja, Micaela Lasser, Connor Monahan, Mayanglambam Dhruba Singh, Dagny J. Gould, Inshya Desai, Laura Anne Lowery, Lucilla Pizzo, Arjun Krishnan, Santhosh Girirajan, Matthew Jensen, Melissa M. Rolls
Publikováno v:
PLoS Genetics, Vol 17, Iss 4, p e1009112 (2021)
PLoS Genetics
PLoS Genetics
We previously identified a deletion on chromosome 16p12.1 that is mostly inherited and associated with multiple neurodevelopmental outcomes, where severely affected probands carried an excess of rare pathogenic variants compared to mildly affected ca
Autor:
Joe Kornegay, Shira T. Rosenblum, Mihail Petrov, Yafeng Song, Andy Mead, Hansell H. Stedman, Phoebe Ingraham, Leon Morales
Publikováno v:
Molecular Therapy. 24:S154
Golden Retriever Muscular Dystrophy (GRMD) dogs frequently develop severe restriction to mouth opening, a condition known as trismus, as one of their earliest physical signs of the disease. Trismus is generally due to fibrosis and/or tonic contractio