Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Rhinda Goedken"'
Autor:
Lorenzo D Botto, Timothy Flood, Julian Little, Mark N Fluchel, Sergey Krikov, Marcia L Feldkamp, Yuan Wu, Rhinda Goedken, Soman Puzhankara, Paul A Romitti
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e69077 (2013)
Birth defects are an increasing health priority worldwide, and the subject of a major 2010 World Health Assembly Resolution. Excess cancer risk may be an added burden in this vulnerable group of children, but studies to date have provided inconsisten
Externí odkaz:
https://doaj.org/article/d9a80c610104448dbe125e3c0aa67602
Autor:
Joan T. Richtsmeier, Rhinda Goedken, Inga Peter, Ethylin Wang Jabs, Xiaoqian Ye, Audrey Guilmatre, Deborah J. Fox, Boris Reva, Yann Heuzé, Paul A. Romitti
Publikováno v:
Plastic and Reconstructive Surgery
Plastic and Reconstructive Surgery, Lippincott, Williams & Wilkins, 2016, 137 (3), pp.952-961. ⟨10.1097/01.prs.0000479978.75545.ee⟩
Plastic and Reconstructive Surgery, Lippincott, Williams & Wilkins, 2016, 137, pp.952-961
Plastic and Reconstructive Surgery, 2016, 137 (3), pp.952-961. ⟨10.1097/01.prs.0000479978.75545.ee⟩
HAL
Plastic and Reconstructive Surgery, Lippincott, Williams & Wilkins, 2016, 137 (3), pp.952-961. ⟨10.1097/01.prs.0000479978.75545.ee⟩
Plastic and Reconstructive Surgery, Lippincott, Williams & Wilkins, 2016, 137, pp.952-961
Plastic and Reconstructive Surgery, 2016, 137 (3), pp.952-961. ⟨10.1097/01.prs.0000479978.75545.ee⟩
HAL
International audience; Background-Craniosynostosis is a condition that includes the premature fusion of one or multiple cranial sutures. Among various craniosynostosis forms, midline sagittal nonsyndromic craniosynostosis (sNSC) is the most prevalen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb51624e134af6d18943664279085932
https://hal.archives-ouvertes.fr/hal-02322637
https://hal.archives-ouvertes.fr/hal-02322637
Autor:
Moyra Smith, Thomas H. Wassink, Rebecca S. Frantz, Joseph Piven, Deb Childress, Laura Jenkins, Christopher W. Bartlett, Val C. Sheffield, M. Anne Spence, Veronica J. Vieland, Rhinda Goedken
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :36-44
Autism is a highly heritable neurodevelopmental syndrome with a complex genetic etiology for which no disease genes have yet been definitively identified. We ascertained three subjects with autism spectrum disorders and chromosome 2q37.3 terminal del
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::310c6cd2a6093a7827dbbe694421f090
https://doi.org/10.1002/ajmg.b.30180
https://doi.org/10.1002/ajmg.b.30180
Autor:
Veronica J. Vieland, Rhinda Goedken, Rebecca S. Frantz, Val C. Sheffield, Molly Losh, Thomas H. Wassink, Joseph Piven
Publikováno v:
Human Genetics. 117:200-206
We report a male child with autism found to have maternal uniparental disomy (UPD) of chromosome 1. The child met diagnostic criteria for the three symptom domains of autism: language impairment, deficient social communication and excessively rigid a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ca81e4b4bc302aea9dd6604e15f198
https://doi.org/10.1007/s00439-005-1257-4
https://doi.org/10.1007/s00439-005-1257-4
Publikováno v:
The American Journal of Human Genetics. 76:688-695
Results of autism linkage studies have been difficult to interpret across research groups, prompting the use of ever-increasing sample sizes to increase power. However, increasing sample size by pooling disparate collections for a single analysis may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56862cab5f93901d7b9a502c38618c4a
https://doi.org/10.1086/429345
https://doi.org/10.1086/429345
Autor:
Susan E. Folstein, Veronica J. Vieland, Thomas H. Wassink, Rhinda Goedken, Jennifer Pietila, Val C. Sheffield, Joseph Piven
Publikováno v:
Molecular Psychiatry. 9:968-972
Impaired reciprocal social interaction is one of the core features of autism. While its determinants are complex, one biomolecular pathway that clearly influences social behavior is the arginine-vasopressin (AVP) system. The behavioral effects of AVP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91305ed1d5e9a69aff382cb17f6c4701
https://doi.org/10.1038/sj.mp.4001503
https://doi.org/10.1038/sj.mp.4001503
Publikováno v:
American Journal of Medical Genetics. :95-99
This article presents a Bayesian re-analysis of a linkage study of panic disorder Crowe et al. [2001: Am J Med Genet (Neuropsychiatr Genet) 105:105-109]. In the initial analysis Crowe et al. failed to find compelling evidence for linkage based on eit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539d44a6ca463036d44dddbfabfbdde0
https://doi.org/10.1002/ajmg.b.20072
https://doi.org/10.1002/ajmg.b.20072
Autor:
Raymond R. Crowe, Steve Samuelson, Jeffrey J. Nelson, Rhinda Goedken, Russell Noyes, Ricky Wilson
Publikováno v:
American Journal of Medical Genetics. 105:105-109
We completed a genome scan of 23 multiplex families of panic disorder. Ninety family members had DSM-III-R panic disorder, and another 23 had recurrent, spontaneous panic attacks that did not satisfy these criteria. We typed 469 markers from the CHLC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba5bfa9c7c3a72e30559308776506203
https://doi.org/10.1002/1096-8628(20010108)105:1<105::aid-ajmg1072>3.0.co
https://doi.org/10.1002/1096-8628(20010108)105:1<105::aid-ajmg1072>3.0.co
Autor:
Susan E. Hodge, Veronica J. Vieland, E. Ludington, Abby J. Fyer, James A. Knowles, Raymond R. Crowe, Myrna M. Weissman, Rhinda Goedken
Publikováno v:
American Journal of Medical Genetics. 96:781-783
Large pedigrees can pose a problem for GENEHUNTER linkage analysis software. Differences in two-point and multipoint lodscores were observed when comparing GENEHUNTER to other linkage software. Careful consideration must be given when selecting linka
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c9f2a9f329b24d1153ae3aecd9d042d
https://doi.org/10.1002/1096-8628(20001204)96:6<781::aid-ajmg17>3.0.co
https://doi.org/10.1002/1096-8628(20001204)96:6<781::aid-ajmg17>3.0.co
Autor:
Thomas H. Wassink, Christopher W. Bartlett, Val C. Sheffield, Joseph Piven, Rhinda Goedken, Veronica J. Vieland, Deborah Childress
To apply phenotypic and statistical methods designed to account for heterogeneity to linkage analyses of the autism Collaborative Linkage Study of Autism (CLSA) affected sibling pair families.The CLSA contains two sets of 57 families each; Set 1 has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd08f9b9226332fd8b0e9f340cd218f2