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Year | Number of Results |
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2008 | 1 |
2009 | 1 |
2010 | 1 |
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Suicidal Crisis among Children and Young People: Associations with Adverse Childhood Experiences and Socio-Demographic Factors.
Int J Environ Res Public Health. 2023 Jan 10;20(2):1251. doi: 10.3390/ijerph20021251.
Int J Environ Res Public Health. 2023.
PMID: 36674021
Free PMC article.
A multidisciplinary team approach to screening, assessment and early intervention for young people with type 1 diabetes and disordered eating behaviour.
Simmons A, McMahon L, Crosbie V, Carlson L.
Simmons A, et al. Among authors: crosbie v.
Clin Child Psychol Psychiatry. 2021 Jul;26(3):629-642. doi: 10.1177/13591045211013872. Epub 2021 May 15.
Clin Child Psychol Psychiatry. 2021.
PMID: 33993742
Item in Clipboard
Structural variation of chromosomes in autism spectrum disorder.
Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW.
Marshall CR, et al. Among authors: crosbie v.
Am J Hum Genet. 2008 Feb;82(2):477-88. doi: 10.1016/j.ajhg.2007.12.009. Epub 2008 Jan 17.
Am J Hum Genet. 2008.
PMID: 18252227
Free PMC article.
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Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Tammimies K, Marshall CR, Walker S, Kaur G, Thiruvahindrapuram B, Lionel AC, Yuen RK, Uddin M, Roberts W, Weksberg R, Woodbury-Smith M, Zwaigenbaum L, Anagnostou E, Wang Z, Wei J, Howe JL, Gazzellone MJ, Lau L, Sung WW, Whitten K, Vardy C, Crosbie V, Tsang B, D'Abate L, Tong WW, Luscombe S, Doyle T, Carter MT, Szatmari P, Stuckless S, Merico D, Stavropoulos DJ, Scherer SW, Fernandez BA.
Tammimies K, et al. Among authors: crosbie v.
JAMA. 2015 Sep 1;314(9):895-903. doi: 10.1001/jama.2015.10078.
JAMA. 2015.
PMID: 26325558
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Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW.
Fernandez BA, et al. Among authors: crosbie v.
J Med Genet. 2010 Mar;47(3):195-203. doi: 10.1136/jmg.2009.069369. Epub 2009 Sep 15.
J Med Genet. 2010.
PMID: 19755429
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