Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Grace F. Porter"'
Autor:
Richard J. Daker, Indre V. Viskontas, Grace F. Porter, Griffin A. Colaizzi, Ian M. Lyons, Adam E. Green
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Identifying ways to enable people to reach their creative potential is a core goal of creativity research with implications for education and professional attainment. Recently, we identified a potential barrier to creative achievement: creat
Externí odkaz:
https://doaj.org/article/56da9769492d442caece0bf237615156
Autor:
Robert A. Cortes, Adam B. Weinberger, Griffin A. Colaizzi, Grace F. Porter, Emily L. Dyke, Holly O. Keaton, Dakota L. Walker, Adam E. Green
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
Relational reasoning is a complex form of human cognition involving the evaluation of relations between mental representations of information. Prior studies have modified stimulus properties of relational reasoning problems and examined differences i
Externí odkaz:
https://doaj.org/article/5a127073e94a440a971f4a6706884566
Autor:
Kathryn A. Johnson, Adam B. Weinberger, Emily Dyke, Grace F. Porter, David J. M. Kraemer, Jordan Grafman, Adam B. Cohen, Adam E. Green
Publikováno v:
Psychology of Religion and Spirituality. 15:128-142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fd9645423fd987e19baa24ba8a53a0e
https://doi.org/10.1037/rel0000460
https://doi.org/10.1037/rel0000460
Autor:
Teresa Sadeghin, Carole A. Samango-Sprouse, Sherida Powell, Andrea L. Gropman, Elizabeth S. Tipton, Grace F. Porter, Patricia C. Lasutschinkow
Publikováno v:
American Journal of Medical Genetics Part A. 185:3541-3546
49,XXXXY was previously associated with profound to severe intellectual deficits. However, prior research papers on the cognitive profiles of this population were confounded by small samples sizes, wide age spreads, and incomplete histories of testos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf71b421540c219d4418ca623ac060c7
https://doi.org/10.1002/ajmg.a.61736
https://doi.org/10.1002/ajmg.a.61736
Autor:
Carole A. Samango-Sprouse, Austin P. Gillies, Andrea L. Gropman, Patricia Hendrie, Grace F. Porter, Francie L. Mitchell, Laura L. Tosi, Patricia C. Lasutschinkow, Selena L. Tran, Leigh Ruland, Elmer N. Rajah, Rick Peret, Teresa Sadeghin
Publikováno v:
American Journal of Medical Genetics Part A. 185:3531-3540
49,XXXXY is the rarest X and Y chromosomal variation, with an incidence of 1 in 80,000-100,000 live male births and has been associated with numerous musculoskeletal abnormalities. Data was collected from an international cohort of boys with 49,XXXXY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7e827e9c7ee45ac1d84713da6d9a6b
https://doi.org/10.1002/ajmg.a.61578
https://doi.org/10.1002/ajmg.a.61578
Autor:
Andrea L. Gropman, Carole A. Samango-Sprouse, Teresa Sadeghin, Patricia C. Lasutschinkow, Selena L. Tran, Grace F. Porter
Publikováno v:
Prenatal Diagnosis. 40:470-480
Objective To investigate the attitudes of parents of children with a sex chromosome aneuploidy (SCA) regarding the impact of an early diagnosis and noninvasive prenatal testing (NIPT). Method A survey consisting of multiple choice and long response f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56337b2fb9b95ef17d7e93a24f1a13bd
https://doi.org/10.1002/pd.5580
https://doi.org/10.1002/pd.5580
Autor:
Grace F. Porter, Carole A. Samango-Sprouse, Andrea L. Gropman, Teresa Sadeghin, Patricia C. Lasutschinkow
Publikováno v:
American Journal of Medical Genetics Part A. 182:974-986
49,XXXXY is a rare X and Y chromosome variation that occurs in 1:85,000 to 1:100,000 live male births and is notable for variable motor, speech, and behavioral deficits. Case studies have described boys with this disorder as shy, impulsive, and aggre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c68fb8603f662c0f4b5fa1e28a6ae3
https://doi.org/10.1002/ajmg.a.61507
https://doi.org/10.1002/ajmg.a.61507
Autor:
Patricia C. Lasutschinkow, Selena L. Tran, Andrea L. Gropman, Carole A. Samango-Sprouse, Grace F. Porter, Debra R Counts
Publikováno v:
The Application of Clinical Genetics. 12:191-202
47,XXY (Klinefelter syndrome [KS]) is the most common sex chromosomal aneuploidy (1:660), yet, despite this, only 25% of the males are ever diagnosed. Males with 47,XXY present with characteristic symptoms throughout their lifetime with typical physi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09d71a0e58dc288924b7eb0e6ab67c03
https://doi.org/10.2147/tacg.s180450
https://doi.org/10.2147/tacg.s180450
Autor:
Carole A. Samango-Sprouse, Jillyan St. Laurent, Sherida Powell, Michael McLeod, Grace F. Porter, Teresa Sadeghin, Andrea L. Gropman, Patricia C. Lasutschinkow
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(12)
49,XXXXY is the rarest X and Y chromosomal variation and is frequently characterized by expressive and receptive language dysfunction, low muscle tonus, and intellectual deficits. Due to the low incidence of this disorder, comprehensive studies analy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b89177d502b94925c0e7401f69c05f4
https://pubmed.ncbi.nlm.nih.gov/32725750
https://pubmed.ncbi.nlm.nih.gov/32725750
Autor:
Sherida Powell, Patricia Hendrie, Patricia C. Lasutschinkow, Francie L. Mitchell, Carole A. Samango-Sprouse, Grace F. Porter, Andrea L. Gropman, Teresa Sadeghin
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(12)
49,XXXXY is a rare chromosomal variation characterized by deficits in motor, language, and cognitive domains. This study reports on the neurological function and dysmorphic features in the largest cohort to date. Seventy-two boys with 49,XXXXY were e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::167227c73bb3a319ccf5b4b3bf4e6692
https://pubmed.ncbi.nlm.nih.gov/32656941
https://pubmed.ncbi.nlm.nih.gov/32656941