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Items: 1 to 20 of 111

1.

Factors Associated with Parental Treatment Attitudes and Information-Seeking Behaviors for Childhood ADHD.

Taylor LE, Antshel KM.

J Atten Disord. 2019 Jan 9:1087054718821734. doi: 10.1177/1087054718821734. [Epub ahead of print]

PMID:
30623746
2.

Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome.

Kikinis Z, Makris N, Sydnor VJ, Bouix S, Pasternak O, Coman IL, Antshel KM, Fremont W, Kubicki MR, Shenton ME, Kates WR, Rathi Y.

Neuroimage Clin. 2018 Nov 27. pii: S2213-1582(18)30364-4. doi: 10.1016/j.nicl.2018.101611. [Epub ahead of print]

3.

The Adult ADHD Quality Measures Initiative.

Faraone SV, Silverstein MJ, Antshel K, Biederman J, Goodman DW, Mason O, Nierenberg AA, Rostain A, Stein MA, Adler LA.

J Atten Disord. 2018 Dec 4:1087054718804354. doi: 10.1177/1087054718804354. [Epub ahead of print]

PMID:
30511593
4.

Childhood Executive Functioning Predicts Young Adult Outcomes in 22q11.2 Deletion Syndrome.

Albert AB, Abu-Ramadan T, Kates WR, Fremont W, Antshel KM.

J Int Neuropsychol Soc. 2018 Oct;24(9):905-916. doi: 10.1017/S1355617718000784.

5.

Trajectories of psychiatric diagnoses and medication usage in youth with 22q11.2 deletion syndrome: a 9-year longitudinal study.

Kates WR, Mariano MA, Antshel KM, Chandra S, Gamble H, Giordano M, MacMaster E, Mattar M, St Fleur D, Faraone SV, Fremont WP.

Psychol Med. 2018 Sep 18:1-9. doi: 10.1017/S0033291718002696. [Epub ahead of print]

PMID:
30226117
6.

Retraction Notice to: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.

Demaerel W, Hestand MS, Vergaelen E, Swillen A, López-Sánchez M, Pérez-Jurado LA, McDonald-McGinn DM, Zackai E, Emanuel BS, Morrow BE, Breckpot J, Devriendt K, Vermeesch JR; International 22q11.2 Brain and Behavior Consortium.

Am J Hum Genet. 2018 Sep 6;103(3):457. doi: 10.1016/j.ajhg.2018.08.011. No abstract available.

7.

Specific differences in temporal binding aspects of the attentional blink in Chromosome 22q11.2 Deletion Syndrome.

Kopec J, Russo N, Antshel KM, Fremont W, Kates WR.

Cortex. 2018 Nov;108:67-79. doi: 10.1016/j.cortex.2018.07.014. Epub 2018 Jul 31.

PMID:
30130634
8.

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.

Sun D, Ching CRK, Lin A, Forsyth JK, Kushan L, Vajdi A, Jalbrzikowski M, Hansen L, Villalon-Reina JE, Qu X, Jonas RK, van Amelsvoort T, Bakker G, Kates WR, Antshel KM, Fremont W, Campbell LE, McCabe KL, Daly E, Gudbrandsen M, Murphy CM, Murphy D, Craig M, Vorstman J, Fiksinski A, Koops S, Ruparel K, Roalf DR, Gur RE, Schmitt JE, Simon TJ, Goodrich-Hunsaker NJ, Durdle CA, Bassett AS, Chow EWC, Butcher NJ, Vila-Rodriguez F, Doherty J, Cunningham A, van den Bree MBM, Linden DEJ, Moss H, Owen MJ, Murphy KC, McDonald-McGinn DM, Emanuel B, van Erp TGM, Turner JA, Thompson PM, Bearden CE.

Mol Psychiatry. 2018 Jun 13. doi: 10.1038/s41380-018-0078-5. [Epub ahead of print]

9.

Young Adult Outcomes for Children With 22q11 Deletion Syndrome and Comorbid ADHD.

Taylor LE, Kates WR, Fremont W, Antshel KM.

J Pediatr Psychol. 2018 Jul 1;43(6):636-644. doi: 10.1093/jpepsy/jsy002.

PMID:
29378061
10.

Frontal dysconnectivity in 22q11.2 deletion syndrome: an atlas-based functional connectivity analysis.

Mattiaccio LM, Coman IL, Thompson CA, Fremont WP, Antshel KM, Kates WR.

Behav Brain Funct. 2018 Jan 20;14(1):2. doi: 10.1186/s12993-018-0134-y.

11.

High intelligence and the risk of ADHD and other psychopathology.

Rommelse N, Antshel K, Smeets S, Greven C, Hoogeveen L, Faraone SV, Hartman CA.

Br J Psychiatry. 2017 Dec;211(6):359-364. doi: 10.1192/bjp.bp.116.184382. Epub 2017 Oct 19.

PMID:
29051177
12.

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.

Demaerel W, Hestand MS, Vergaelen E, Swillen A, López-Sánchez M, Pérez-Jurado LA, McDonald-McGinn DM, Zackai E, Emanuel BS, Morrow BE, Breckpot J, Devriendt K, Vermeesch JR; International 22q11.2 Brain and Behavior Consortium.

Am J Hum Genet. 2017 Oct 5;101(4):616-622. doi: 10.1016/j.ajhg.2017.09.002. Epub 2017 Sep 28. Retraction in: Am J Hum Genet. 2018 Sep 6;103(3):457.

13.

Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study.

Tylee DS, Kikinis Z, Quinn TP, Antshel KM, Fremont W, Tahir MA, Zhu A, Gong X, Glatt SJ, Coman IL, Shenton ME, Kates WR, Makris N.

Neuroimage Clin. 2017 May 11;15:832-842. doi: 10.1016/j.nicl.2017.04.029. eCollection 2017.

14.

Childhood Predictors of Young Adult Social Functioning in 22q11.2 Deletion Syndrome.

Wagner KE, Kates WR, Fremont W, Antshel KM.

J Autism Dev Disord. 2017 Aug;47(8):2480-2501. doi: 10.1007/s10803-017-3165-6.

15.

Inattention and Hyperactivity-Impulsivity: Their Detrimental Effect on Romantic Relationship Maintenance.

VanderDrift LE, Antshel KM, Olszewski AK.

J Atten Disord. 2017 May 1:1087054717707043. doi: 10.1177/1087054717707043. [Epub ahead of print]

PMID:
28490222
16.

Systematic Review and Meta-analysis of Intelligence Quotient in Early-Treated Individuals with Classical Galactosemia.

Welling L, Waisbren SE, Antshel KM, Colhoun HO, Gautschi M, Grünewald S, Holman R, van der Lee JH, Treacy EP, Bosch AM.

JIMD Rep. 2017;37:115-123. doi: 10.1007/8904_2017_22. Epub 2017 Apr 9.

17.

Childhood predictors of written expression in late adolescents with 22q11.2 deletion syndrome: a longitudinal study.

Hamsho N, Antshel KM, Eckert TL, Kates WR.

J Intellect Disabil Res. 2017 May;61(5):501-511. doi: 10.1111/jir.12370. Epub 2017 Mar 8.

18.

The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study.

Olszewski AK, Kikinis Z, Gonzalez CS, Coman IL, Makris N, Gong X, Rathi Y, Zhu A, Antshel KM, Fremont W, Kubicki MR, Bouix S, Shenton ME, Kates WR.

Behav Brain Funct. 2017 Feb 16;13(1):4. doi: 10.1186/s12993-017-0122-7.

19.

Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study.

Weisman O, Guri Y, Gur RE, McDonald-McGinn DM, Calkins ME, Tang SX, Emanuel B, Zackai EH, Eliez S, Schneider M, Schaer M, Kates WR, Antshel KM, Fremont W, Shashi V, Hooper SR, Armando M, Vicari S, Pontillo M, Kushan L, Jalbrzikowski M, Bearden CE, Cubells JF, Ousley OY, Walker EF, Simon TJ, Stoddard J, Niendam TA, van den Bree MBM, Gothelf D; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Schizophr Bull. 2017 Sep 1;43(5):1079-1089. doi: 10.1093/schbul/sbx005.

20.

Developmental psychopathology in the post-genomics era - substantial challenges but reasons for hope.

Halperin JM.

J Child Psychol Psychiatry. 2017 Mar;58(3):219-221. doi: 10.1111/jcpp.12708.

PMID:
28194760

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