Kates WR - Search Results

1

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.

Chawner SJRA, Doherty JL, Anney RJL, Antshel KM, Bearden CE, Bernier R, Chung WK, Clements CC, Curran SR, Cuturilo G, Fiksinski AM, Gallagher L, Goin-Kochel RP, Gur RE, Hanson E, Jacquemont S, Kates WR, Kushan L, Maillard AM, McDonald-McGinn DM, Mihaljevic M, Miller JS, Moss H, Pejovic-Milovancevic M, Schultz RT, Green-Snyder L, Vorstman JA, Wenger TL; IMAGINE-ID Consortium; Hall J, Owen MJ, van den Bree MBM. Chawner SJRA, et al. Among authors: kates wr. Am J Psychiatry. 2021 Jan 1;178(1):77-86. doi: 10.1176/appi.ajp.2020.20010015. Am J Psychiatry. 2021. PMID: 33384013 Free PMC article.

2

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords.

Antshel KM, Kates WR, Roizen N, Fremont W, Shprintzen RJ. Antshel KM, et al. Among authors: kates wr. Child Neuropsychol. 2005 Feb;11(1):5-19. doi: 10.1080/09297040590911185. Child Neuropsychol. 2005. PMID: 15823980 Review.

3

Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).

Antshel KM, Conchelos J, Lanzetta G, Fremont W, Kates WR. Antshel KM, et al. Among authors: kates wr. Psychiatry Res. 2005 Apr 30;138(3):235-45. doi: 10.1016/j.pscychresns.2005.02.003. Psychiatry Res. 2005. PMID: 15854791

4

A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).

Kates WR, Antshel KM, Abdulsabur N, Colgan D, Funke B, Fremont W, Higgins AM, Kucherlapati R, Shprintzen RJ. Kates WR, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):274-80. doi: 10.1002/ajmg.b.30284. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16511839 Free PMC article.

5

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).

Kates WR, Miller AM, Abdulsabur N, Antshel KM, Conchelos J, Fremont W, Roizen N. Kates WR, et al. J Am Acad Child Adolesc Psychiatry. 2006 May;45(5):587-595. doi: 10.1097/01.chi.0000205704.33077.4a. J Am Acad Child Adolesc Psychiatry. 2006. PMID: 16670653

6

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

Antshel KM, Fremont W, Roizen NJ, Shprintzen R, Higgins AM, Dhamoon A, Kates WR. Antshel KM, et al. Among authors: kates wr. J Am Acad Child Adolesc Psychiatry. 2006 May;45(5):596-603. doi: 10.1097/01.chi.0000205703.25453.5a. J Am Acad Child Adolesc Psychiatry. 2006. PMID: 16670654

7

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

Antshel KM, Aneja A, Strunge L, Peebles J, Fremont WP, Stallone K, Abdulsabur N, Higgins AM, Shprintzen RJ, Kates WR. Antshel KM, et al. Among authors: kates wr. J Autism Dev Disord. 2007 Oct;37(9):1776-86. doi: 10.1007/s10803-006-0308-6. Epub 2006 Dec 19. J Autism Dev Disord. 2007. PMID: 17180713

8

Manic symptoms and behavioral dysregulation in youth with velocardiofacial syndrome (22q11.2 deletion syndrome).

Aneja A, Fremont WP, Antshel KM, Faraone SV, AbdulSabur N, Higgins AM, Shprintzen R, Kates WR. Aneja A, et al. Among authors: kates wr. J Child Adolesc Psychopharmacol. 2007 Feb;17(1):105-14. doi: 10.1089/cap.2006.0023. J Child Adolesc Psychopharmacol. 2007. PMID: 17343558

9

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome).

Kates WR, Krauss BR, Abdulsabur N, Colgan D, Antshel KM, Higgins AM, Shprintzen RJ. Kates WR, et al. Neuropsychologia. 2007 Sep 20;45(12):2863-73. doi: 10.1016/j.neuropsychologia.2007.05.007. Epub 2007 May 24. Neuropsychologia. 2007. PMID: 17618656 Free PMC article.

10

Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism.

Kates WR, Antshel KM, Fremont WP, Shprintzen RJ, Strunge LA, Burnette CP, Higgins AM. Kates WR, et al. Am J Med Genet A. 2007 Nov 15;143A(22):2642-50. doi: 10.1002/ajmg.a.32012. Am J Med Genet A. 2007. PMID: 17937445

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