Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Emily A, Malouf"'
Autor:
Nandana D. Rao, Jailanie Kaganovsky, Emily A. Malouf, Sandy Coe, Jennifer Huey, Darwin Tsinajinne, Sajida Hassan, Kristine M. King, Stephanie M. Fullerton, Annie T. Chen, Brian H. Shirts
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-12 (2023)
Abstract Background Population screening for genetic risk of adult-onset preventable conditions has been proposed as an attractive public health intervention. Screening unselected individuals can identify many individuals who will not be identified t
Externí odkaz:
https://doaj.org/article/aaf51ee5b0d0495b9871dde4e113e737
Autor:
Annie T Chen, Jennifer Huey, Sandra Coe, Jailanie Kaganovsky, Emily A Malouf, Heather D Evans, Jill Daker, Elizabeth Harper, Olivia Fordiani, Emma E Lowe, Caileigh McGraw Oldroyd, Ashlyn Price, Kristlynn Roth, Julie Stoddard, Jill N Crandell, Brian H Shirts
Publikováno v:
JMIR Cancer, Vol 9, p e43126 (2023)
BackgroundCascade screening, defined as helping at-risk relatives get targeted genetic testing of familial variants for dominant hereditary cancer syndromes, is a proven component of cancer prevention; however, its uptake is low. We developed and con
Externí odkaz:
https://doaj.org/article/86dd2a16763945c09af78f86d5509f26
Autor:
Xinxian Deng, He Fang, Asha Pathak, Angela M. Zou, Whitney Neufeld-Kaiser, Emily A. Malouf, Richard A. Failor, Fuki M. Hisama, Yajuan J. Liu
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundHypergonadotropic hypogonadism (HH) is characterized by low sex steroid levels and secondarily elevated gonadotropin levels with either congenital or acquired etiology. Genetic factors leading to HH have yet to be fully elucidated.MethodsHe
Externí odkaz:
https://doaj.org/article/3dc4d9f2c90a4f2f956fd8f281eb4c74
Autor:
Annie T Chen, Jennifer Huey, Sandra Coe, Jailanie Kaganovsky, Emily A Malouf, Heather D Evans, Jill Daker, Elizabeth Harper, Olivia Fordiani, Emma E Lowe, Caileigh McGraw Oldroyd, Ashlyn Price, Kristlynn Roth, Julie Stoddard, Jill N Crandell, Brian H Shirts
BACKGROUND Cascade screening, defined as helping at-risk relatives get targeted genetic testing of familial variants for dominant hereditary cancer syndromes, is a proven component of cancer prevention; however, its uptake is low. We developed and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b6b9de329307926482d3db1ed0c8915
https://doi.org/10.2196/preprints.43126
https://doi.org/10.2196/preprints.43126
Publikováno v:
Rehabilitation Counseling Bulletin. :003435522311552
As vocational rehabilitation (VR) agencies continue to implement provisions of the Workforce Innovation and Opportunity Act (WIOA) to provide employment-related transition services to youth with disabilities, it is unclear if implementation plans inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e72038573c43981c123f4d2a30ed4c8d
https://doi.org/10.1177/00343552231155218
https://doi.org/10.1177/00343552231155218
Autor:
Xinxian, Deng, He, Fang, Asha, Pathak, Angela M, Zou, Whitney, Neufeld-Kaiser, Emily A, Malouf, Richard A, Failor, Fuki M, Hisama, Yajuan J, Liu
Publikováno v:
Frontiers in Genetics
Background Hypergonadotropic hypogonadism (HH) is characterized by low sex steroid levels and secondarily elevated gonadotropin levels with either congenital or acquired etiology. Genetic factors leading to HH have yet to be fully elucidated. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52b3f72ab03382550b8da9fe554d49e1
https://pubmed.ncbi.nlm.nih.gov/33193636
https://pubmed.ncbi.nlm.nih.gov/33193636
Publikováno v:
Muscle Nerve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e9ae20bb23c559dcbb326f45bca4ea
https://doi.org/10.1002/mus.26658
https://doi.org/10.1002/mus.26658
Autor:
Emily A. Malouf, Suman Jayadev, Michael D. Weiss, Robin L. Bennett, Jie Feng, C. Ronald Scott, Heather M. Byers
Publikováno v:
JIMD Reports ISBN: 9783662536803
Serine is a nonessential amino acid that plays a vital role in proper development and functioning of the central nervous system (CNS). Serine deficiency leads to microcephaly, intellectual disability, seizures, and psychomotor retardation in children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::839f96ae3e00604c4e3e02d3be4e3d19
https://doi.org/10.1007/8904_2015_510
https://doi.org/10.1007/8904_2015_510