Fremont WP - Search Results

1

Novel genome-wide associations for effort valuation and psychopathology in children and adults.

Nguyen NH, Mazza TM, Hess JL, Albert AB, Elfstrom S, Forken P, Blatt SD, Fremont WP, Faraone SV, Glatt SJ. Nguyen NH, et al. Among authors: fremont wp. Am J Med Genet B Neuropsychiatr Genet. 2024 Jun;195(4):e32964. doi: 10.1002/ajmg.b.32964. Epub 2023 Nov 12. Am J Med Genet B Neuropsychiatr Genet. 2024. PMID: 37953388

2

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: fremont wp. J Child Adolesc Psychopharmacol. 2007 Feb;17(1):105-14. doi: 10.1089/cap.2006.0023. J Child Adolesc Psychopharmacol. 2007. PMID: 17343558

3

Comparing ADHD in velocardiofacial syndrome to idiopathic ADHD: a preliminary study.

Antshel KM, Faraone SV, Fremont W, Monuteaux MC, Kates WR, Doyle A, Mick E, Biederman J. Antshel KM, et al. J Atten Disord. 2007 Jul;11(1):64-73. doi: 10.1177/1087054707299397. J Atten Disord. 2007. PMID: 17606773

4

Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study.

Antshel KM, Shprintzen R, Fremont W, Higgins AM, Faraone SV, Kates WR. Antshel KM, et al. J Am Acad Child Adolesc Psychiatry. 2010 Apr;49(4):333-44. J Am Acad Child Adolesc Psychiatry. 2010. PMID: 20410726 Free PMC article.

5

Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study.

Kates WR, Antshel KM, Faraone SV, Fremont WP, Higgins AM, Shprintzen RJ, Botti JA, Kelchner L, McCarthy C. Kates WR, et al. Among authors: fremont wp. Biol Psychiatry. 2011 May 15;69(10):945-52. doi: 10.1016/j.biopsych.2010.10.027. Epub 2010 Dec 31. Biol Psychiatry. 2011. PMID: 21195387 Free PMC article.

6

The longitudinal course of attention deficit/hyperactivity disorder in velo-cardio-facial syndrome.

Antshel KM, Hendricks K, Shprintzen R, Fremont W, Higgins AM, Faraone SV, Kates WR. Antshel KM, et al. J Pediatr. 2013 Jul;163(1):187-93.e1. doi: 10.1016/j.jpeds.2012.12.026. Epub 2013 Jan 18. J Pediatr. 2013. PMID: 23337092 Free PMC article.

7

Predicting reading comprehension academic achievement in late adolescents with velo-cardio-facial (22q11.2 deletion) syndrome (VCFS): a longitudinal study.

Antshel K, Hier B, Fremont W, Faraone SV, Kates W. Antshel K, et al. J Intellect Disabil Res. 2014 Oct;58(10):926-39. doi: 10.1111/jir.12134. Epub 2014 May 26. J Intellect Disabil Res. 2014. PMID: 24861691 Free PMC article.

8

Neurocognitive and familial moderators of psychiatric risk in velocardiofacial (22q11.2 deletion) syndrome: a longitudinal study.

Kates WR, Russo N, Wood WM, Antshel KM, Faraone SV, Fremont WP. Kates WR, et al. Among authors: fremont wp. Psychol Med. 2015 Jun;45(8):1629-39. doi: 10.1017/S0033291714002724. Epub 2014 Nov 14. Psychol Med. 2015. PMID: 25394491

9

Longitudinal trajectories of cortical thickness as a biomarker for psychosis in individuals with 22q11.2 deletion syndrome.

Ramanathan S, Mattiaccio LM, Coman IL, Botti JC, Fremont W, Faraone SV, Antshel KM, Kates WR. Ramanathan S, et al. Schizophr Res. 2017 Oct;188:35-41. doi: 10.1016/j.schres.2016.11.041. Epub 2016 Dec 15. Schizophr Res. 2017. PMID: 27988073

10

Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.

Thompson CA, Karelis J, Middleton FA, Gentile K, Coman IL, Radoeva PD, Mehta R, Fremont WP, Antshel KM, Faraone SV, Kates WR. Thompson CA, et al. Among authors: fremont wp. Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):295-314. doi: 10.1002/ajmg.b.32515. Epub 2017 Jan 31. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28139055

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