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Department/Unit:Child and Adolescent Psychiatry

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11507


An in-home intervention program for children with mental health needs

Lindsey, Michael A; Lee, Bethany R; Sullivan, Francis A
PMID: 19176425
ISSN: 1557-9700
CID: 1850762

Functional brain correlates of social and nonsocial processes in autism spectrum disorders: an activation likelihood estimation meta-analysis

Di Martino, Adriana; Ross, Kathryn; Uddin, Lucina Q; Sklar, Andrew B; Castellanos, F Xavier; Milham, Michael P
BACKGROUND: Functional neuroimaging studies of autism spectrum disorders (ASD) have examined social and nonsocial paradigms, although rarely in the same study. Here, we provide an objective, unbiased survey of functional brain abnormalities in ASD, related to both social and nonsocial processing. METHODS: We conducted two separate voxel-wise activation likelihood estimation meta-analyses of 39 functional neuroimaging studies consisting of 24 studies examining social processes (e.g., theory of mind, face perception) and 15 studies examining nonsocial processes (e.g., attention control, working memory). Voxel-wise significance threshold was p<.05, corrected by false discovery rate. RESULTS: Compared with neurotypical control (NC) subjects, ASD showed greater likelihood of hypoactivation in two medial wall regions: perigenual anterior cingulate cortex (ACC) in social tasks only and dorsal ACC in nonsocial studies. Further, right anterior insula, recently linked to social cognition, was more likely to be hypoactivated in ASD in the analyses of social studies. In nonsocial studies, group comparisons showed greater likelihood of activation for the ASD group in the rostral ACC region that is typically suppressed during attentionally demanding tasks. CONCLUSIONS: Despite substantial heterogeneity of tasks, the rapidly increasing functional imaging literature showed ASD-related patterns of hypofunction and aberrant activation that depended on the specific cognitive domain, i.e., social versus nonsocial. These results provide a basis for targeted extensions of these findings with younger subjects and a range of paradigms, including analyses of default mode network regulation in ASD
PMCID:2993772
PMID: 18996505
ISSN: 1873-2402
CID: 97447

Toward the dimensionome: parsing reward-related processing in attention-deficit/hyperactivity disorder [Comment]

Castellanos, F Xavier
PMID: 19064036
ISSN: 1873-2402
CID: 97451

A HAPLOTYPE IN THE MSRA GENE APPEARS TO CONFER DECREASED RISK OF MECONIUM ILEUS IN CF [Meeting Abstract]

Henderson, LB; Doshi, VK; Blackman, SM; Naughton, KM; Pace, RG; Drumm, ML; Knowles, MR; Cutting, GR
ISI:000270703400241
ISSN: 8755-6863
CID: 2738102

GENOME-WIDE LINKAGE FOR LUNG FUNCTION MEASURES IN CYSTIC FIBROSIS [Meeting Abstract]

Doshi, VK; Blackman, SM; Collaco, JM; Corey, M; Durie, PR
ISI:000270703400269
ISSN: 8755-6863
CID: 2738222

Relationship between apathy and cognitive abilities in depressed PD patients [Meeting Abstract]

Morrison, C.; Varanese, S.; Hirsch, S.; Howard, J.; Hamid, H.; Di Rocco, A.
ISI:000266618101136
ISSN: 0885-3185
CID: 591382

Limitations of traditional screening tools to detect depression in Parkinson's disease [Meeting Abstract]

Howard, J. F.; Varanese, S.; Penesetti, D.; Morrison, C.; Hirsch, S.; Brown, R.; DiRocco, A.
ISI:000266618100697
ISSN: 0885-3185
CID: 591402

2007 Update on allogeneic islet transplantation from the Collaborative Islet Transplant Registry (CITR)

Shapiro, A M J; Lakey, J; Ryan, E; Baker, S; Bourne, W; Dinyari, P; McCready, T; Trasbourg, C; LaBranche, K; Menon, V; Sarmon, D; Reswell, B; Wright, J; Alejandro, R; Ricordi, C; Baidal, D; Blanco-Jivanjee, Y; Cereijo, J; Cure, P; Froud, T; Hafiz, M; Khan, A; Perez, M I; Rothenberg, L; Silva-Ramos, M; Hering, B J; Ansite, J; Bland, B; Duderstadt, K; Gibson, C; Hodges, K; Jevne, R; Larson, V; Radosevich, D; Spindler, D; Zylla, D; Parkey, J; Kramer, C; Nettles, A; Pattou, F; Ezzouaoui, R; Gmyr, V; Kerr-Conte, J; Raverdy, V; Vantyghem, M C; Naji, A; Markmann, E M; McLaughlin, D; Palanjian, M; Deng, S; Goss, J A; Durkop, C; Schock, P; Zgabay, T; Goodpastor, S; Inman, S; Mote, A; Cagliero, E; Dea, A; Omer, A K; Turgeon, H; Weir, G; Kandeel, F; Chen, L; Hacker, J; Ikle, D; Longmate, J; Mullen, Y; Santiago, J; Shiang, K D; Lesiecki, L; Omori, K; LaRose, A; Garfinkel, M; Boone, P; Roberts, M; Skarbek, R; Connors, M; Shah, M; Zhao, P; Lockwood, M; Thomas, S; Murphy, P; Rusk, K; Oberholzer, J; Benedetti, E; Bui, J; Hatipoglu, B; Owens, C; West, D; Avila, J; Hansen, M; Kaplan, B; Martellotto, J; Nash, K; Romagnoli, T; Sadat, K; Salehi, P; Smith, C; Larsen, C; Holbrook, E; Sanders, E; Sears, M; Joseph, J; Hanson, M; Radke, N; Desai, N; Kemp, D; Olack, B; O'Brien, L; Robertson, H; Kaufman, D; Pellar, S; Olszewski, B; Stuart, E; Al-Saden, P; Reinhart, N; Levy, M; Grimes, D; Otken, L; Naziruddin, B; Rossini, A; Hartigan, C; Thompson, M; Wiseman, A; Britz, B; Gill, R; Sours, E; Valentine, A; Wallace, A; Weiner, L; Westbrook, K; Bishop, J; George, S; Stock, P; Posselt, A; Bluestone, J; McElroy, J; Garwood, C; Szot, G; Ramos, D; Rojas, T; Worden, M; Gaber, A O; Bogard, D; Culbreath, B; Fraga, D; Lo, A; McGee-Wilson, D; Greenbaum, C; McCulloch-Olson, M; Reeve, M; Brayman, K; Korsun, A; Langman, L; Carveth, B; Simmons, W; Ketchum, R; Hanschew, M; Marks, W; Baker, T; Levy, G; Cattral, M; Adcock, L; Donat, D; Sheedy, J; Wright, E; Gores, P; Sauzier, G; Williams, D; McGraw, M; Herold, K; Hardy, M A; Comninel, S; Guo, Q; Bader, S; Kelly, J; Liu, Z; Ruiz, E -P; Witkowski, P; Barton, F B; Wease, S; Stablein, D; Damodharan, Y; Mandzuk, C; Heitman, A; Cravens, J; Calaway, B; Long, J; Wagner, C; Danoff, R
As of October 1, 2007, 25 North American medical institutions and one European islet transplant center reported detailed information to the Registry on 315 allograft recipients, of which 285 were islet alone (IA) and 30 were islet after kidney (IAK). Of the 114 IA recipients expected at 4 years after their last infusion, 12% were insulin independent, 16% were insulin dependent with detectable C-peptide, 40% had no detectable C-peptide, and 32% had missing C-peptide data or were lost to follow-up. Of the IA recipients, 72% achieved insulin independence at least once over 3 years and multiple infusions. Factors associated with achievement of insulin independence included islet size >1.0 expressed as IEQs per islet number [hazard ratio (HR) = 1.5, p = 0.06], additional infusions given (HR = 1.5, p = 0.01), lower pretransplant HbA 1c (HR = 1.2 each %-age unit, p = 0.02), donor given insulin (HR = 2, p = 0.003), daclizumab given at any infusion (HR = 1.9, p = 0.06), and shorter cold storage time (HR = 1.04, p = 0.03), mutually adjusted in a multivariate model. Severe hypoglycemia prevalence was reduced from 78-83% preinfusion to less than 5% throughout the first year post-last infusion, and to 18% adjusted for missing data at 3 years post-last infusion. In Year 1 post-first infusion for IA recipients, 53% experienced a Grade 3-5 or serious adverse event (AE) and 35% experienced a severe AE related to either an infusion procedure or immunosuppression. In Year 1 post-first infusion, 33% of IA subjects and 35% of IAK subjects had an AE related to the infusion procedure, while 35% of IA subjects and only 27% of IAK subjects had an AE related to the immunosuppression therapy. Five deaths were reported, of which two were classified as probably related to the infusion procedure or immunosuppression, and 10 cases of neoplasm, of which two were classified as probably related to the procedure or immunosuppression. Islet transplantation continues to show short-term benefits of insulin independence, normal or near normal HbA1C levels, and sustained marked decrease in hypoglycemic episodes.
EMBASE:355556120
ISSN: 0963-6897
CID: 4302972

Partitioning of Functional Data for Understanding Heterogeneity in Psychiatric Conditions

Petkova, E; Tarpey, T
PMCID:2844078
PMID: 20336166
ISSN: 1938-7989
CID: 156322

Smoothing parameter selection for a class of semiparametric linear models

Reiss, PT; Ogden RT
Spline-based approaches to non-parametric and semiparametric regression, as well as to regression of scalar outcomes on functional predictors, entail choosing a parameter controlling the extent to which roughness of the fitted function is penalized. We demonstrate that the equations determining two popular methods for smoothing parameter selection, generalized cross-validation and restricted maximum likelihood, share a similar form that allows us to prove several results which are common to both, and to derive a condition under which they yield identical values. These ideas are illustrated by application of functional principal component regression, a method for regressing scalars on functions, to two chemometric data sets. $$:
ISI:000264374200008
ISSN: 1369-7412
CID: 99262