Cited In for PMID: 11121177

Year	Number of Results
2000	1
2002	1
2003	3
2005	1
2006	1
2009	1
2010	1
2011	2
2012	2
2013	1
2015	1
2023	1
2026	0

1

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

Smith M, Filipek PA, Wu C, Bocian M, Hakim S, Modahl C, Spence MA. Smith M, et al. Am J Med Genet. 2000 Dec 4;96(6):765-70. doi: 10.1002/1096-8628(20001204)96:6<765::aid-ajmg13>3.0.co;2-l. Am J Med Genet. 2000. PMID: 11121177 Free article.

2

Regulation of MAPK Signaling Pathways by the Large HERC Ubiquitin Ligases.

Sala-Gaston J, Costa-Sastre L, Pedrazza L, Martinez-Martinez A, Ventura F, Rosa JL. Sala-Gaston J, et al. Int J Mol Sci. 2023 Mar 3;24(5):4906. doi: 10.3390/ijms24054906. Int J Mol Sci. 2023. PMID: 36902336 Free PMC article. Review.

3

De novo interstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case.

Kim HS, Han JY, Kim MJ. Kim HS, et al. Korean J Pediatr. 2015 Aug;58(8):313-6. doi: 10.3345/kjp.2015.58.8.313. Epub 2015 Aug 21. Korean J Pediatr. 2015. PMID: 26388897 Free PMC article.

4

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.

Behjati F, Firouzabadi SG, Kariminejad R, Vameghi R, Sajedi F, Shafaghati Y, Ghasemlou BE, Shojaei A, Jamali P, Bahman I, Najmabadi H. Behjati F, et al. Indian J Hum Genet. 2013 Oct;19(4):443-8. doi: 10.4103/0971-6866.124373. Indian J Hum Genet. 2013. PMID: 24497710 Free PMC article.

5

Mitochondrial and ion channel gene alterations in autism.

Smith M, Flodman PL, Gargus JJ, Simon MT, Verrell K, Haas R, Reiner GE, Naviaux R, Osann K, Spence MA, Wallace DC. Smith M, et al. Biochim Biophys Acta. 2012 Oct;1817(10):1796-802. doi: 10.1016/j.bbabio.2012.04.004. Epub 2012 Apr 17. Biochim Biophys Acta. 2012. PMID: 22538295 Free PMC article. Clinical Trial.

6

Chromosome 15q24 microdeletion syndrome.

Magoulas PL, El-Hattab AW. Magoulas PL, et al. Orphanet J Rare Dis. 2012 Jan 4;7:2. doi: 10.1186/1750-1172-7-2. Orphanet J Rare Dis. 2012. PMID: 22216833 Free PMC article. Review.

7

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain.

Kochunov P, Glahn DC, Nichols TE, Winkler AM, Hong EL, Holcomb HH, Stein JL, Thompson PM, Curran JE, Carless MA, Olvera RL, Johnson MP, Cole SA, Kochunov V, Kent J, Blangero J. Kochunov P, et al. Front Neurosci. 2011 Oct 19;5:120. doi: 10.3389/fnins.2011.00120. eCollection 2011. Front Neurosci. 2011. PMID: 22028680 Free PMC article.

8

Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21.

Cukier HN, Salyakina D, Blankstein SF, Robinson JL, Sacharow S, Ma D, Wright HH, Abramson RK, Menon R, Williams SM, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Cukier HN, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jun;156B(4):493-501. doi: 10.1002/ajmg.b.31188. Epub 2011 Apr 7. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21480499 Free PMC article.

9

A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.

McInnes LA, Nakamine A, Pilorge M, Brandt T, Jiménez González P, Fallas M, Manghi ER, Edelmann L, Glessner J, Hakonarson H, Betancur C, Buxbaum JD. McInnes LA, et al. Mol Autism. 2010 Mar 19;1(1):5. doi: 10.1186/2040-2392-1-5. Mol Autism. 2010. PMID: 20678247 Free PMC article.

10

Stomatin-like protein-1 interacts with stomatin and is targeted to late endosomes.

Mairhofer M, Steiner M, Salzer U, Prohaska R. Mairhofer M, et al. J Biol Chem. 2009 Oct 16;284(42):29218-29. doi: 10.1074/jbc.M109.014993. Epub 2009 Aug 20. J Biol Chem. 2009. PMID: 19696025 Free PMC article.

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Cited In for PMID: 11121177

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