AHI1 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "AHI1" in English language version.

refsWebsite

Global rank English rank

10nih.gov

4^th place

5doi.org

2^nd place

2worldcat.org

5^th place

2ensembl.org

1,626^th place

1,007^th place

1umich.edu

459^th place

360^th place

1handle.net

102^nd place

76^th place

1semanticscholar.org

11^th place

8^th place

doi.org

Dixon-Salazar T, Silhavy JL, Marsh SE, Louie CM, Scott LC, Gururaj A, Al-Gazali L, Al-Tawari AA, Kayserili H (2004-12-01). "Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria". American Journal of Human Genetics. 75 (6): 979–987. doi:10.1086/425985. ISSN 0002-9297. PMC 1182159. PMID 15467982.
Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M (2006-06-14). "AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia". European Journal of Human Genetics. 14 (10): 1111–1119. doi:10.1038/sj.ejhg.5201675. ISSN 1018-4813. PMID 16773125.
Lotan A, Lifschytz T, Slonimsky A, Broner EC, Greenbaum L, Abedat S, Fellig Y, Cohen H, Lory O (2014). "Neural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disorders". Molecular Psychiatry. 19 (2): 243–252. doi:10.1038/mp.2013.123. PMID 24042478.
Lagier-Tourenne C, Boltshauser E, Breivik N, Gribaa M, Betard C, Barbot C, Koenig M (Apr 2004). "Homozygosity mapping of a third Joubert syndrome locus to 6q23". J Med Genet. 41 (4): 273–7. doi:10.1136/jmg.2003.014787. PMC 1735723. PMID 15060101.
Utsch B, Sayer JA, Attanasio M, Pereira RR, Eccles M, Hennies HC, Otto EA, Hildebrandt F (Mar 2006). "Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome" (PDF). Pediatr Nephrol. 21 (1): 32–5. doi:10.1007/s00467-005-2054-y. hdl:2027.42/47827. PMID 16240161. S2CID 18955859.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000135541 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000019986 – Ensembl, May 2017

handle.net

hdl.handle.net

Utsch B, Sayer JA, Attanasio M, Pereira RR, Eccles M, Hennies HC, Otto EA, Hildebrandt F (Mar 2006). "Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome" (PDF). Pediatr Nephrol. 21 (1): 32–5. doi:10.1007/s00467-005-2054-y. hdl:2027.42/47827. PMID 16240161. S2CID 18955859.

nih.gov

ncbi.nlm.nih.gov

Dixon-Salazar T, Silhavy JL, Marsh SE, Louie CM, Scott LC, Gururaj A, Al-Gazali L, Al-Tawari AA, Kayserili H (2004-12-01). "Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria". American Journal of Human Genetics. 75 (6): 979–987. doi:10.1086/425985. ISSN 0002-9297. PMC 1182159. PMID 15467982.
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Lagier-Tourenne C, Boltshauser E, Breivik N, Gribaa M, Betard C, Barbot C, Koenig M (Apr 2004). "Homozygosity mapping of a third Joubert syndrome locus to 6q23". J Med Genet. 41 (4): 273–7. doi:10.1136/jmg.2003.014787. PMC 1735723. PMID 15060101.
"Entrez Gene: AHI1 Abelson helper integration site 1".

pubmed.ncbi.nlm.nih.gov

Dixon-Salazar T, Silhavy JL, Marsh SE, Louie CM, Scott LC, Gururaj A, Al-Gazali L, Al-Tawari AA, Kayserili H (2004-12-01). "Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria". American Journal of Human Genetics. 75 (6): 979–987. doi:10.1086/425985. ISSN 0002-9297. PMC 1182159. PMID 15467982.
Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M (2006-06-14). "AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia". European Journal of Human Genetics. 14 (10): 1111–1119. doi:10.1038/sj.ejhg.5201675. ISSN 1018-4813. PMID 16773125.
Lotan A, Lifschytz T, Slonimsky A, Broner EC, Greenbaum L, Abedat S, Fellig Y, Cohen H, Lory O (2014). "Neural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disorders". Molecular Psychiatry. 19 (2): 243–252. doi:10.1038/mp.2013.123. PMID 24042478.
Lagier-Tourenne C, Boltshauser E, Breivik N, Gribaa M, Betard C, Barbot C, Koenig M (Apr 2004). "Homozygosity mapping of a third Joubert syndrome locus to 6q23". J Med Genet. 41 (4): 273–7. doi:10.1136/jmg.2003.014787. PMC 1735723. PMID 15060101.
Utsch B, Sayer JA, Attanasio M, Pereira RR, Eccles M, Hennies HC, Otto EA, Hildebrandt F (Mar 2006). "Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome" (PDF). Pediatr Nephrol. 21 (1): 32–5. doi:10.1007/s00467-005-2054-y. hdl:2027.42/47827. PMID 16240161. S2CID 18955859.

semanticscholar.org

api.semanticscholar.org

Utsch B, Sayer JA, Attanasio M, Pereira RR, Eccles M, Hennies HC, Otto EA, Hildebrandt F (Mar 2006). "Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome" (PDF). Pediatr Nephrol. 21 (1): 32–5. doi:10.1007/s00467-005-2054-y. hdl:2027.42/47827. PMID 16240161. S2CID 18955859.

umich.edu

deepblue.lib.umich.edu

Utsch B, Sayer JA, Attanasio M, Pereira RR, Eccles M, Hennies HC, Otto EA, Hildebrandt F (Mar 2006). "Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome" (PDF). Pediatr Nephrol. 21 (1): 32–5. doi:10.1007/s00467-005-2054-y. hdl:2027.42/47827. PMID 16240161. S2CID 18955859.

worldcat.org

search.worldcat.org

Dixon-Salazar T, Silhavy JL, Marsh SE, Louie CM, Scott LC, Gururaj A, Al-Gazali L, Al-Tawari AA, Kayserili H (2004-12-01). "Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria". American Journal of Human Genetics. 75 (6): 979–987. doi:10.1086/425985. ISSN 0002-9297. PMC 1182159. PMID 15467982.
Amann-Zalcenstein D, Avidan N, Kanyas K, Ebstein RP, Kohn Y, Hamdan A, Ben-Asher E, Karni O, Mujaheed M (2006-06-14). "AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia". European Journal of Human Genetics. 14 (10): 1111–1119. doi:10.1038/sj.ejhg.5201675. ISSN 1018-4813. PMID 16773125.