Curry–Jones syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Curry–Jones syndrome" in English language version.

refsWebsite

Global rank English rank

7nih.gov

4^th place

6doi.org

2^nd place

6worldcat.org

5^th place

1orpha.net

3,537^th place

7,177^th place

1omim.org

4,380^th place

4,305^th place

1semanticscholar.org

11^th place

8^th place

doi.org

Twigg, Stephen R. F.; Hufnagel, Robert B.; Miller, Kerry A.; Zhou, Yan; McGowan, Simon J.; Taylor, John; Craft, Jude; Taylor, Jenny C.; Santoro, Stephanie L.; Huang, Taosheng; Hopkin, Robert J. (2016-06-02). "A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome". American Journal of Human Genetics. 98 (6): 1256–1265. doi:10.1016/j.ajhg.2016.04.007. ISSN 1537-6605. PMC 4908219. PMID 27236920.
Temple, I. K.; Eccles, D. M.; Winter, R. M.; Baraitser, M.; Carr, S. B.; Shortland, D.; Jones, M. C.; Curry, C. (1995-04-01). "Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome". Clinical Dysmorphology. 4 (2): 116–129. doi:10.1097/00019605-199504000-00003. ISSN 0962-8827. PMID 7606318.
Mingarelli, R.; Mokini, V.; Castriota Scanderbeg, A.; Dallapiccola, B. (1999-01-01). "Brachycephalosyndactyly with ptosis, cataract, colobomas, and linear areas of skin depigmentation". Clinical Dysmorphology. 8 (1): 73–75. doi:10.1097/00019605-199901000-00015. ISSN 0962-8827. PMID 10327257.
Thomas, Ellen R. A.; Wakeling, Emma L.; Goodman, Frances R.; Dickinson, John C.; Hall, Christine M.; Brady, Angela F. (2006-04-01). "Mild case of Curry-Jones syndrome". Clinical Dysmorphology. 15 (2): 115–117. doi:10.1097/01.mcd.0000194406.85052.de. ISSN 1473-5717. PMID 16531740.
Grange, Dorothy K.; Clericuzio, Carol L.; Bayliss, Susan J.; Berk, David R.; Heideman, Richard L.; Higginson, Julie K.; Julian, Stephanie; Lind, Anne (2008-10-15). "Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway". American Journal of Medical Genetics. Part A. 146A (20): 2589–2597. doi:10.1002/ajmg.a.32503. ISSN 1552-4833. PMID 18798318. S2CID 12265879.
Cohen, M. M. (1988). "Craniosynostosis update 1987". American Journal of Medical Genetics. Supplement. 4: 99–148. doi:10.1002/ajmg.1320310514. ISSN 1040-3787. PMID 3144990.

nih.gov

pubmed.ncbi.nlm.nih.gov

Twigg, Stephen R. F.; Hufnagel, Robert B.; Miller, Kerry A.; Zhou, Yan; McGowan, Simon J.; Taylor, John; Craft, Jude; Taylor, Jenny C.; Santoro, Stephanie L.; Huang, Taosheng; Hopkin, Robert J. (2016-06-02). "A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome". American Journal of Human Genetics. 98 (6): 1256–1265. doi:10.1016/j.ajhg.2016.04.007. ISSN 1537-6605. PMC 4908219. PMID 27236920.
Temple, I. K.; Eccles, D. M.; Winter, R. M.; Baraitser, M.; Carr, S. B.; Shortland, D.; Jones, M. C.; Curry, C. (1995-04-01). "Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome". Clinical Dysmorphology. 4 (2): 116–129. doi:10.1097/00019605-199504000-00003. ISSN 0962-8827. PMID 7606318.
Mingarelli, R.; Mokini, V.; Castriota Scanderbeg, A.; Dallapiccola, B. (1999-01-01). "Brachycephalosyndactyly with ptosis, cataract, colobomas, and linear areas of skin depigmentation". Clinical Dysmorphology. 8 (1): 73–75. doi:10.1097/00019605-199901000-00015. ISSN 0962-8827. PMID 10327257.
Thomas, Ellen R. A.; Wakeling, Emma L.; Goodman, Frances R.; Dickinson, John C.; Hall, Christine M.; Brady, Angela F. (2006-04-01). "Mild case of Curry-Jones syndrome". Clinical Dysmorphology. 15 (2): 115–117. doi:10.1097/01.mcd.0000194406.85052.de. ISSN 1473-5717. PMID 16531740.
Grange, Dorothy K.; Clericuzio, Carol L.; Bayliss, Susan J.; Berk, David R.; Heideman, Richard L.; Higginson, Julie K.; Julian, Stephanie; Lind, Anne (2008-10-15). "Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway". American Journal of Medical Genetics. Part A. 146A (20): 2589–2597. doi:10.1002/ajmg.a.32503. ISSN 1552-4833. PMID 18798318. S2CID 12265879.
Cohen, M. M. (1988). "Craniosynostosis update 1987". American Journal of Medical Genetics. Supplement. 4: 99–148. doi:10.1002/ajmg.1320310514. ISSN 1040-3787. PMID 3144990.

ncbi.nlm.nih.gov

Twigg, Stephen R. F.; Hufnagel, Robert B.; Miller, Kerry A.; Zhou, Yan; McGowan, Simon J.; Taylor, John; Craft, Jude; Taylor, Jenny C.; Santoro, Stephanie L.; Huang, Taosheng; Hopkin, Robert J. (2016-06-02). "A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome". American Journal of Human Genetics. 98 (6): 1256–1265. doi:10.1016/j.ajhg.2016.04.007. ISSN 1537-6605. PMC 4908219. PMID 27236920.

omim.org

"OMIM Entry - # 601707 - Curry-Jones Syndrome; CRJS". www.omim.org. Retrieved 2022-06-29.

orpha.net

"Orphanet: Curry Jones syndrome". www.orpha.net. Retrieved 2022-06-29.

semanticscholar.org

api.semanticscholar.org

Grange, Dorothy K.; Clericuzio, Carol L.; Bayliss, Susan J.; Berk, David R.; Heideman, Richard L.; Higginson, Julie K.; Julian, Stephanie; Lind, Anne (2008-10-15). "Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway". American Journal of Medical Genetics. Part A. 146A (20): 2589–2597. doi:10.1002/ajmg.a.32503. ISSN 1552-4833. PMID 18798318. S2CID 12265879.

worldcat.org

Twigg, Stephen R. F.; Hufnagel, Robert B.; Miller, Kerry A.; Zhou, Yan; McGowan, Simon J.; Taylor, John; Craft, Jude; Taylor, Jenny C.; Santoro, Stephanie L.; Huang, Taosheng; Hopkin, Robert J. (2016-06-02). "A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome". American Journal of Human Genetics. 98 (6): 1256–1265. doi:10.1016/j.ajhg.2016.04.007. ISSN 1537-6605. PMC 4908219. PMID 27236920.
Temple, I. K.; Eccles, D. M.; Winter, R. M.; Baraitser, M.; Carr, S. B.; Shortland, D.; Jones, M. C.; Curry, C. (1995-04-01). "Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome". Clinical Dysmorphology. 4 (2): 116–129. doi:10.1097/00019605-199504000-00003. ISSN 0962-8827. PMID 7606318.
Mingarelli, R.; Mokini, V.; Castriota Scanderbeg, A.; Dallapiccola, B. (1999-01-01). "Brachycephalosyndactyly with ptosis, cataract, colobomas, and linear areas of skin depigmentation". Clinical Dysmorphology. 8 (1): 73–75. doi:10.1097/00019605-199901000-00015. ISSN 0962-8827. PMID 10327257.
Thomas, Ellen R. A.; Wakeling, Emma L.; Goodman, Frances R.; Dickinson, John C.; Hall, Christine M.; Brady, Angela F. (2006-04-01). "Mild case of Curry-Jones syndrome". Clinical Dysmorphology. 15 (2): 115–117. doi:10.1097/01.mcd.0000194406.85052.de. ISSN 1473-5717. PMID 16531740.
Grange, Dorothy K.; Clericuzio, Carol L.; Bayliss, Susan J.; Berk, David R.; Heideman, Richard L.; Higginson, Julie K.; Julian, Stephanie; Lind, Anne (2008-10-15). "Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway". American Journal of Medical Genetics. Part A. 146A (20): 2589–2597. doi:10.1002/ajmg.a.32503. ISSN 1552-4833. PMID 18798318. S2CID 12265879.
Cohen, M. M. (1988). "Craniosynostosis update 1987". American Journal of Medical Genetics. Supplement. 4: 99–148. doi:10.1002/ajmg.1320310514. ISSN 1040-3787. PMID 3144990.