Isodicentric 15 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Isodicentric 15" in English language version.

refsWebsite

Global rank English rank

16nih.gov

4^th place

8doi.org

2^nd place

5web.archive.org

1^st place

1orpha.net

3,537^th place

7,177^th place

1worldcat.org

5^th place

1idic15.org

low place

1semanticscholar.org

11^th place

8^th place

1exploringautism.org

low place

1aaas.org

9,065^th place

7,557^th place

1dup15q.org

low place

1harvard.edu

18^th place

17^th place

aaas.org

"Science Translational Medicine: Making Mice with Autistic Behavior". Archived from the original on 2013-12-03. Retrieved 2012-03-22.

doi.org

Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Chen CP, Lin HY, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Fran S, Chen YY, Town DD, Pan CW, Wang W (July 2020). "Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)". Taiwanese Journal of Obstetrics & Gynecology. 59 (4): 580–585. doi:10.1016/j.tjog.2020.05.019. PMID 32653133.
Hogart, Amber; Wu, David; Lasalle, Janine M.; Schanen, N. Carolyn (2008). "The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.1". Neurobiology of Disease. 38 (2): 181–191. doi:10.1016/j.nbd.2008.08.011. PMC 2884398. PMID 18840528.
Luchsinger, Kadi; Lau, Heather; Hedlund, Julie L; Friedman, Daniel; Krushel, Kara; Devinsky, Orrin (2016). "Parental-reported pain insensitivity in Dup15q". Epilepsy & Behavior. 55: 124–7. doi:10.1016/j.yebeh.2015.10.007. PMID 26773682. S2CID 32626204.
Smith, S. E. P.; Zhou, Y.-D.; Zhang, G.; Jin, Z.; Stoppel, D. C.; Anderson, M. P. (2011). "Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice". Science Translational Medicine. 3 (103): 103ra97. doi:10.1126/scitranslmed.3002627. PMC 3356696. PMID 21974935.
Wang N.J.; Liu D.; Parokonny A.S.; Schanen N.C. (2004). "High-resolution molecular characterization of 15q11–q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage". Am. J. Hum. Genet. 75 (2): 267–281. doi:10.1086/422854. PMC 1216061. PMID 15197683.
Battaglia A (2008). "The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)". Orphanet J Rare Dis. 3: 30. doi:10.1186/1750-1172-3-30. PMC 2613132. PMID 19019226.
Frohlich J., Senturk D., Saravanapandian V., Golshani P., Reiter L.T., Sankar R., Thibert R.L., DiStefano C., Huberty S., Cook E.H., Jeste S.S. (2016). "A Quantitative Electrophysiological Biomarker of Duplication 15q11. 2-q13. 1 Syndrome". PLOS ONE. 11 (12): e0167179. Bibcode:2016PLoSO..1167179F. doi:10.1371/journal.pone.0167179. PMC 5157977. PMID 27977700.{{cite journal}}: CS1 maint: multiple names: authors list (link)

dup15q.org

"Physician Advisory - Dup15q". 8 April 2014. Archived from the original on 17 October 2017. Retrieved 17 October 2017.

exploringautism.org

"Archived copy". Archived from the original on 2010-03-05. Retrieved 2010-04-04.{{cite web}}: CS1 maint: archived copy as title (link)

harvard.edu

ui.adsabs.harvard.edu

Frohlich J., Senturk D., Saravanapandian V., Golshani P., Reiter L.T., Sankar R., Thibert R.L., DiStefano C., Huberty S., Cook E.H., Jeste S.S. (2016). "A Quantitative Electrophysiological Biomarker of Duplication 15q11. 2-q13. 1 Syndrome". PLOS ONE. 11 (12): e0167179. Bibcode:2016PLoSO..1167179F. doi:10.1371/journal.pone.0167179. PMC 5157977. PMID 27977700.{{cite journal}}: CS1 maint: multiple names: authors list (link)

idic15.org

"IDEAS - Isodicentric 15 | Welcome to IDEAS: IsoDicentric 15 Exchange Advocacy and Support | Support and Advocacy for duplication 15q syndrome: IDIC15, IDIC(15), Interstitial d..." Archived from the original on June 4, 2008.

nih.gov

pubmed.ncbi.nlm.nih.gov

Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Chen CP, Lin HY, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Fran S, Chen YY, Town DD, Pan CW, Wang W (July 2020). "Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)". Taiwanese Journal of Obstetrics & Gynecology. 59 (4): 580–585. doi:10.1016/j.tjog.2020.05.019. PMID 32653133.
Hogart, Amber; Wu, David; Lasalle, Janine M.; Schanen, N. Carolyn (2008). "The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.1". Neurobiology of Disease. 38 (2): 181–191. doi:10.1016/j.nbd.2008.08.011. PMC 2884398. PMID 18840528.
Luchsinger, Kadi; Lau, Heather; Hedlund, Julie L; Friedman, Daniel; Krushel, Kara; Devinsky, Orrin (2016). "Parental-reported pain insensitivity in Dup15q". Epilepsy & Behavior. 55: 124–7. doi:10.1016/j.yebeh.2015.10.007. PMID 26773682. S2CID 32626204.
Cook E.H. Jr; Lindgren V.; Leventhal B.L.; Courchesne R.; Lincoln A.; Shulman C.; Lord C.; Courchesne E. (1997). "Autism or atypical autism in maternally but not paternally derived proximal 15q duplication". Am. J. Hum. Genet. 60 (4): 928–934. PMC 1712464. PMID 9106540.
Smith, S. E. P.; Zhou, Y.-D.; Zhang, G.; Jin, Z.; Stoppel, D. C.; Anderson, M. P. (2011). "Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice". Science Translational Medicine. 3 (103): 103ra97. doi:10.1126/scitranslmed.3002627. PMC 3356696. PMID 21974935.
Wang N.J.; Liu D.; Parokonny A.S.; Schanen N.C. (2004). "High-resolution molecular characterization of 15q11–q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage". Am. J. Hum. Genet. 75 (2): 267–281. doi:10.1086/422854. PMC 1216061. PMID 15197683.
Battaglia A (2008). "The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)". Orphanet J Rare Dis. 3: 30. doi:10.1186/1750-1172-3-30. PMC 2613132. PMID 19019226.
Frohlich J., Senturk D., Saravanapandian V., Golshani P., Reiter L.T., Sankar R., Thibert R.L., DiStefano C., Huberty S., Cook E.H., Jeste S.S. (2016). "A Quantitative Electrophysiological Biomarker of Duplication 15q11. 2-q13. 1 Syndrome". PLOS ONE. 11 (12): e0167179. Bibcode:2016PLoSO..1167179F. doi:10.1371/journal.pone.0167179. PMC 5157977. PMID 27977700.{{cite journal}}: CS1 maint: multiple names: authors list (link)

ncbi.nlm.nih.gov

Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Hogart, Amber; Wu, David; Lasalle, Janine M.; Schanen, N. Carolyn (2008). "The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.1". Neurobiology of Disease. 38 (2): 181–191. doi:10.1016/j.nbd.2008.08.011. PMC 2884398. PMID 18840528.
Cook E.H. Jr; Lindgren V.; Leventhal B.L.; Courchesne R.; Lincoln A.; Shulman C.; Lord C.; Courchesne E. (1997). "Autism or atypical autism in maternally but not paternally derived proximal 15q duplication". Am. J. Hum. Genet. 60 (4): 928–934. PMC 1712464. PMID 9106540.
Smith, S. E. P.; Zhou, Y.-D.; Zhang, G.; Jin, Z.; Stoppel, D. C.; Anderson, M. P. (2011). "Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice". Science Translational Medicine. 3 (103): 103ra97. doi:10.1126/scitranslmed.3002627. PMC 3356696. PMID 21974935.
Wang N.J.; Liu D.; Parokonny A.S.; Schanen N.C. (2004). "High-resolution molecular characterization of 15q11–q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage". Am. J. Hum. Genet. 75 (2): 267–281. doi:10.1086/422854. PMC 1216061. PMID 15197683.
Battaglia A (2008). "The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)". Orphanet J Rare Dis. 3: 30. doi:10.1186/1750-1172-3-30. PMC 2613132. PMID 19019226.
Frohlich J., Senturk D., Saravanapandian V., Golshani P., Reiter L.T., Sankar R., Thibert R.L., DiStefano C., Huberty S., Cook E.H., Jeste S.S. (2016). "A Quantitative Electrophysiological Biomarker of Duplication 15q11. 2-q13. 1 Syndrome". PLOS ONE. 11 (12): e0167179. Bibcode:2016PLoSO..1167179F. doi:10.1371/journal.pone.0167179. PMC 5157977. PMID 27977700.{{cite journal}}: CS1 maint: multiple names: authors list (link)

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Duplication/inversion 15q11". www.orpha.net. Archived from the original on 30 April 2018. Retrieved 22 May 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)

semanticscholar.org

api.semanticscholar.org

Luchsinger, Kadi; Lau, Heather; Hedlund, Julie L; Friedman, Daniel; Krushel, Kara; Devinsky, Orrin (2016). "Parental-reported pain insensitivity in Dup15q". Epilepsy & Behavior. 55: 124–7. doi:10.1016/j.yebeh.2015.10.007. PMID 26773682. S2CID 32626204.

web.archive.org

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Duplication/inversion 15q11". www.orpha.net. Archived from the original on 30 April 2018. Retrieved 22 May 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
"IDEAS - Isodicentric 15 | Welcome to IDEAS: IsoDicentric 15 Exchange Advocacy and Support | Support and Advocacy for duplication 15q syndrome: IDIC15, IDIC(15), Interstitial d..." Archived from the original on June 4, 2008.
"Archived copy". Archived from the original on 2010-03-05. Retrieved 2010-04-04.{{cite web}}: CS1 maint: archived copy as title (link)
"Science Translational Medicine: Making Mice with Autistic Behavior". Archived from the original on 2013-12-03. Retrieved 2012-03-22.
"Physician Advisory - Dup15q". 8 April 2014. Archived from the original on 17 October 2017. Retrieved 17 October 2017.

worldcat.org

Gardner, R. J. M. (2012). Chromosome abnormalities and genetic counseling. Grant R. Sutherland, Lisa G. Shaffer (4th ed.). Oxford: Oxford University Press. p. 306. ISBN 978-0-19-974915-7. OCLC 769344040.