FOXP2 (Turkish Wikipedia)

Analysis of information sources in references of the Wikipedia article "FOXP2" in Turkish language version.

refsWebsite

Global rank Turkish rank

11nih.gov

4^th place

11^th place

9doi.org

2^nd place

4^th place

3web.archive.org

1^st place

2archive.org

6^th place

1ensembl.org

1,626^th place

3,843^rd place

1harvard.edu

18^th place

47^th place

1univ-montp2.fr

low place

1sciencemag.org

857^th place

573^rd place

1human-brain.org

low place

archive.org

MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE (Haziran 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. 76 (6). ss. 1074-80. doi:10.1086/430841. PMC 1196445 $2. PMID 15877281.
Fisher SE, Scharff C (Nisan 2009). "FOXP2 as a molecular window into speech and language". Trends in Genetics. 25 (4). ss. 166-77. doi:10.1016/j.tig.2009.03.002. PMID 19304338.

doi.org

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (Ekim 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855). ss. 519-23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. PMID 11586359.
Nudel R, Newbury DF (Eylül 2013). "FOXP2". Wiley Interdisciplinary Reviews: Cognitive Science. 4 (5). ss. 547-560. doi:10.1002/wcs.1247. PMC 3992897 $2. PMID 24765219.
Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (Şubat 1998). "Localisation of a gene implicated in a severe speech and language disorder". Nature Genetics. 18 (2). ss. 168-70. doi:10.1038/ng0298-168. PMID 9462748.
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP (Ağustos 2000). "The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder". American Journal of Human Genetics. 67 (2). ss. 357-68. doi:10.1086/303011. PMC 1287211 $2. PMID 10880297.
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE (Haziran 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. 76 (6). ss. 1074-80. doi:10.1086/430841. PMC 1196445 $2. PMID 15877281.
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE (Mart 2008). "Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits". Current Biology. 18 (5). ss. 354-62. doi:10.1016/j.cub.2008.01.060. PMC 2917768 $2. PMID 18328704.
Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C (Aralık 2007). "Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X". PLoS Biology. 5 (12). ss. e321. doi:10.1371/journal.pbio.0050321. PMC 2100148 $2. PMID 18052609.
Fisher SE, Scharff C (Nisan 2009). "FOXP2 as a molecular window into speech and language". Trends in Genetics. 25 (4). ss. 166-77. doi:10.1016/j.tig.2009.03.002. PMID 19304338.
Shu W, Lu MM, Zhang Y, Tucker PW, Zhou D, Morrisey EE (Mayıs 2007). "Foxp2 and Foxp1 cooperatively regulate lung and esophagus development". Development. 134 (10). ss. 1991-2000. doi:10.1242/dev.02846. PMID 17428829.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000128573 - Ensembl, May 2017

harvard.edu

adsabs.harvard.edu

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (Ekim 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855). ss. 519-23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. PMID 11586359.

human-brain.org

Harpaz Y. "Language gene found". human-brain.org. 25 Ekim 2014 tarihinde kaynağından arşivlendi. Erişim tarihi: 31 Ekim 2014.

nih.gov

ncbi.nlm.nih.gov

"İnsan PubMed Başvurusu:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Fare PubMed Başvurusu:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (Ekim 2001). "A forkhead-domain gene is mutated in a severe speech and language disorder". Nature. 413 (6855). ss. 519-23. Bibcode:2001Natur.413..519L. doi:10.1038/35097076. PMID 11586359.
Nudel R, Newbury DF (Eylül 2013). "FOXP2". Wiley Interdisciplinary Reviews: Cognitive Science. 4 (5). ss. 547-560. doi:10.1002/wcs.1247. PMC 3992897 $2. PMID 24765219.
Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME (Şubat 1998). "Localisation of a gene implicated in a severe speech and language disorder". Nature Genetics. 18 (2). ss. 168-70. doi:10.1038/ng0298-168. PMID 9462748.
Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP (Ağustos 2000). "The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder". American Journal of Human Genetics. 67 (2). ss. 357-68. doi:10.1086/303011. PMC 1287211 $2. PMID 10880297.
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE (Haziran 2005). "Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits". American Journal of Human Genetics. 76 (6). ss. 1074-80. doi:10.1086/430841. PMC 1196445 $2. PMID 15877281.
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE (Mart 2008). "Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits". Current Biology. 18 (5). ss. 354-62. doi:10.1016/j.cub.2008.01.060. PMC 2917768 $2. PMID 18328704.
Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C (Aralık 2007). "Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X". PLoS Biology. 5 (12). ss. e321. doi:10.1371/journal.pbio.0050321. PMC 2100148 $2. PMID 18052609.
Fisher SE, Scharff C (Nisan 2009). "FOXP2 as a molecular window into speech and language". Trends in Genetics. 25 (4). ss. 166-77. doi:10.1016/j.tig.2009.03.002. PMID 19304338.
Shu W, Lu MM, Zhang Y, Tucker PW, Zhou D, Morrisey EE (Mayıs 2007). "Foxp2 and Foxp1 cooperatively regulate lung and esophagus development". Development. 134 (10). ss. 1991-2000. doi:10.1242/dev.02846. PMID 17428829.

sciencemag.org

news.sciencemag.org

Pennisi E (31 Ekim 2013). "'Language Gene' Has a Partner". Science. 5 Ekim 2014 tarihinde kaynağından arşivlendi. Erişim tarihi: 30 Ekim 2014.

univ-montp2.fr

orthomam.univ-montp2.fr

"OrthoMaM phylogenetic marker: FOXP2 coding sequence". 23 Mart 2017 tarihinde kaynağından arşivlendi. Erişim tarihi: 18 Şubat 2010.

web.archive.org

"OrthoMaM phylogenetic marker: FOXP2 coding sequence". 23 Mart 2017 tarihinde kaynağından arşivlendi. Erişim tarihi: 18 Şubat 2010.
Pennisi E (31 Ekim 2013). "'Language Gene' Has a Partner". Science. 5 Ekim 2014 tarihinde kaynağından arşivlendi. Erişim tarihi: 30 Ekim 2014.
Harpaz Y. "Language gene found". human-brain.org. 25 Ekim 2014 tarihinde kaynağından arşivlendi. Erişim tarihi: 31 Ekim 2014.