Nukleotido bakarreko polimorfismo (Basque Wikipedia)

Analysis of information sources in references of the Wikipedia article "Nukleotido bakarreko polimorfismo" in Basque language version.

refsWebsite

Global rank Basque rank

35nih.gov

4^th place

5^th place

19doi.org

2^nd place

6^th place

16worldcat.org

5^th place

1^st place

1nature.com

234^th place

64^th place

1pnas.org

1,293^rd place

141^st place

1acs.org

1,248^th place

377^th place

1genome.gov

9,308^th place

1,436^th place

1snpedia.com

low place

1hgvs-nomenclature.org

low place

1elsevier.com

610^th place

142^nd place

acs.org

pubs.acs.org

(Ingelesez) Griffin, Timothy J.; Smith, Lloyd M.. (2000-07-01). «Genetic Identification by Mass Spectrometric Analysis of Single-Nucleotide Polymorphisms: Ternary Encoding of Genotypes» Analytical Chemistry 72 (14): 3298–3302. doi:10.1021/ac991390e. ISSN 0003-2700. (Noiz kontsultatua: 2024-03-10).

doi.org

dx.doi.org

Sherry, S. T.. (2001-01-01). «dbSNP: the NCBI database of genetic variation» Nucleic Acids Research 29 (1): 308–311. doi:10.1093/nar/29.1.308. ISSN 1362-4962. PMID 11125122. PMC PMC29783. (Noiz kontsultatua: 2024-03-10).
Spencer, Paige S.; Barral, José M.. (2012). «Genetic code redundancy and its influence on the encoded polypeptides» Computational and Structural Biotechnology Journal 1: e201204006. doi:10.5936/csbj.201204006. ISSN 2001-0370. PMID 24688635. PMC 3962081. (Noiz kontsultatua: 2024-03-10).
Chu, Duan; Wei, Lai. (2019-04-16). «Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation» BMC cancer 19 (1): 359. doi:10.1186/s12885-019-5572-x. ISSN 1471-2407. PMID 30991970. PMC 6469204. (Noiz kontsultatua: 2024-03-10).
Kimchi-Sarfaty, Chava; Oh, Jung Mi; Kim, In-Wha; Sauna, Zuben E.; Calcagno, Anna Maria; Ambudkar, Suresh V.; Gottesman, Michael M.. (2007-01-26). «A "silent" polymorphism in the MDR1 gene changes substrate specificity» Science (New York, N.Y.) 315 (5811): 525–528. doi:10.1126/science.1135308. ISSN 1095-9203. PMID 17185560. (Noiz kontsultatua: 2024-03-10).
Al-Haggar, Mohammad; Madej-Pilarczyk, Agnieszka; Kozlowski, Lukasz; Bujnicki, Janusz M.; Yahia, Sohier; Abdel-Hadi, Dina; Shams, Amany; Ahmad, Nermin et al.. (2012-11). «A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome» European journal of human genetics: EJHG 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. ISSN 1476-5438. PMID 22549407. PMC 3476705. (Noiz kontsultatua: 2024-03-10).
Cordovado, S. K.; Hendrix, M.; Greene, C. N.; Mochal, S.; Earley, M. C.; Farrell, P. M.; Kharrazi, M.; Hannon, W. H. et al.. (2012-02). «CFTR mutation analysis and haplotype associations in CF patients» Molecular Genetics and Metabolism 105 (2): 249–254. doi:10.1016/j.ymgme.2011.10.013. ISSN 1096-7206. PMID 22137130. PMC 3551260. (Noiz kontsultatua: 2024-03-10).
Lu, Yi-Fan; Mauger, David M.; Goldstein, David B.; Urban, Thomas J.; Weeks, Kevin M.; Bradrick, Shelton S.. (2015-11-04). «IFNL3 mRNA structure is remodeled by a functional non-coding polymorphism associated with hepatitis C virus clearance» Scientific Reports 5: 16037. doi:10.1038/srep16037. ISSN 2045-2322. PMID 26531896. PMC 4631997. (Noiz kontsultatua: 2024-03-10).
Altshuler, D.; Pollara, V. J.; Cowles, C. R.; Van Etten, W. J.; Baldwin, J.; Linton, L.; Lander, E. S.. (2000-09-28). «An SNP map of the human genome generated by reduced representation shotgun sequencing» Nature 407 (6803): 513–516. doi:10.1038/35035083. ISSN 0028-0836. PMID 11029002. (Noiz kontsultatua: 2024-03-10).
(Ingelesez) Telenti, Amalio; Pierce, Levi C. T.; Biggs, William H.; di Iulio, Julia; Wong, Emily H. M.; Fabani, Martin M.; Kirkness, Ewen F.; Moustafa, Ahmed et al.. (2016-10-18). «Deep sequencing of 10,000 human genomes» Proceedings of the National Academy of Sciences 113 (42): 11901–11906. doi:10.1073/pnas.1613365113. ISSN 0027-8424. PMID 27702888. PMC PMC5081584. (Noiz kontsultatua: 2024-03-10).
(Ingelesez) Griffin, Timothy J.; Smith, Lloyd M.. (2000-07-01). «Genetic Identification by Mass Spectrometric Analysis of Single-Nucleotide Polymorphisms: Ternary Encoding of Genotypes» Analytical Chemistry 72 (14): 3298–3302. doi:10.1021/ac991390e. ISSN 0003-2700. (Noiz kontsultatua: 2024-03-10).
Tahira, Tomoko; Kukita, Yoji; Higasa, Koichiro; Okazaki, Yuko; Yoshinaga, Aki; Hayashi, Kenshi. (2009). «Estimation of SNP allele frequencies by SSCP analysis of pooled DNA» Methods in Molecular Biology (Clifton, N.J.) 578: 193–207. doi:10.1007/978-1-60327-411-1_12. ISSN 1940-6029. PMID 19768595. (Noiz kontsultatua: 2024-03-10).
Ogino, Shuji; Gulley, Margaret L.; den Dunnen, Johan T.; Wilson, Robert B.. (2007-2). «Standard Mutation Nomenclature in Molecular Diagnostics» The Journal of molecular diagnostics : JMD 9 (1): 1–6. doi:10.2353/jmoldx.2007.060081. ISSN 1525-1578. PMID 17251329. PMC 1867422. (Noiz kontsultatua: 2024-03-10).
(Ingelesez) Giegling, Ina; Hartmann, Annette M.; Möller, Hans-Jürgen; Rujescu, Dan. (2006-11). «Anger- and aggression-related traits are associated with polymorphisms in the 5-HT-2A gene» Journal of Affective Disorders 96 (1-2): 75–81. doi:10.1016/j.jad.2006.05.016. (Noiz kontsultatua: 2024-03-10).
Kujovich, Jody Lynn. (2011-01). «Factor V Leiden thrombophilia» Genetics in Medicine 13 (1): 1–16. doi:10.1097/gim.0b013e3181faa0f2. ISSN 1098-3600. (Noiz kontsultatua: 2024-03-10).
Morita, Akihiko; Nakayama, Tomohiro; Doba, Nobutaka; Hinohara, Shigeaki; Mizutani, Tomohiko; Soma, Masayoshi. (2007-06). «Genotyping of triallelic SNPs using TaqMan PCR» Molecular and Cellular Probes 21 (3): 171–176. doi:10.1016/j.mcp.2006.10.005. ISSN 0890-8508. PMID 17161935. (Noiz kontsultatua: 2024-03-10).
Prodi, D. A.; Drayna, D.; Forabosco, P.; Palmas, M. A.; Maestrale, G. B.; Piras, D.; Pirastu, M.; Angius, A.. (2004-10). «Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene» Chemical Senses 29 (8): 697–702. doi:10.1093/chemse/bjh074. ISSN 0379-864X. PMID 15466815. (Noiz kontsultatua: 2024-03-10).
Wolpin, Brian M.; Rizzato, Cosmeri; Kraft, Peter; Kooperberg, Charles; Petersen, Gloria M.; Wang, Zhaoming; Arslan, Alan A.; Beane-Freeman, Laura et al.. (2014-09). «Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer» Nature Genetics 46 (9): 994–1000. doi:10.1038/ng.3052. ISSN 1546-1718. PMID 25086665. PMC 4191666. (Noiz kontsultatua: 2024-03-10).

doi.org

Sherry, S. T.. (2001-01-01). «dbSNP: the NCBI database of genetic variation» Nucleic Acids Research 29 (1): 308–311. doi:10.1093/nar/29.1.308. ISSN 1362-4962. PMID 11125122. PMC PMC29783. (Noiz kontsultatua: 2024-03-10).
Kujovich, Jody Lynn. (2011-01). «Factor V Leiden thrombophilia» Genetics in Medicine 13 (1): 1–16. doi:10.1097/gim.0b013e3181faa0f2. ISSN 1098-3600. (Noiz kontsultatua: 2024-03-10).

elsevier.com

linkinghub.elsevier.com

(Ingelesez) Giegling, Ina; Hartmann, Annette M.; Möller, Hans-Jürgen; Rujescu, Dan. (2006-11). «Anger- and aggression-related traits are associated with polymorphisms in the 5-HT-2A gene» Journal of Affective Disorders 96 (1-2): 75–81. doi:10.1016/j.jad.2006.05.016. (Noiz kontsultatua: 2024-03-10).

genome.gov

(Gaztelaniaz) «HapMap (mapa de haplotipos) | NHGRI» www.genome.gov (Noiz kontsultatua: 2024-03-10).

hgvs-nomenclature.org

«General - HGVS Nomenclature» hgvs-nomenclature.org (Noiz kontsultatua: 2024-03-10).

nature.com

(Ingelesez) «Polygenic Inheritance and Gene Mapping | Learn Science at Scitable» www.nature.com (Noiz kontsultatua: 2024-03-10).

nih.gov

ncbi.nlm.nih.gov

Sherry, S. T.. (2001-01-01). «dbSNP: the NCBI database of genetic variation» Nucleic Acids Research 29 (1): 308–311. doi:10.1093/nar/29.1.308. ISSN 1362-4962. PMID 11125122. PMC PMC29783. (Noiz kontsultatua: 2024-03-10).
Spencer, Paige S.; Barral, José M.. (2012). «Genetic code redundancy and its influence on the encoded polypeptides» Computational and Structural Biotechnology Journal 1: e201204006. doi:10.5936/csbj.201204006. ISSN 2001-0370. PMID 24688635. PMC 3962081. (Noiz kontsultatua: 2024-03-10).
Chu, Duan; Wei, Lai. (2019-04-16). «Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation» BMC cancer 19 (1): 359. doi:10.1186/s12885-019-5572-x. ISSN 1471-2407. PMID 30991970. PMC 6469204. (Noiz kontsultatua: 2024-03-10).
Kimchi-Sarfaty, Chava; Oh, Jung Mi; Kim, In-Wha; Sauna, Zuben E.; Calcagno, Anna Maria; Ambudkar, Suresh V.; Gottesman, Michael M.. (2007-01-26). «A "silent" polymorphism in the MDR1 gene changes substrate specificity» Science (New York, N.Y.) 315 (5811): 525–528. doi:10.1126/science.1135308. ISSN 1095-9203. PMID 17185560. (Noiz kontsultatua: 2024-03-10).
Al-Haggar, Mohammad; Madej-Pilarczyk, Agnieszka; Kozlowski, Lukasz; Bujnicki, Janusz M.; Yahia, Sohier; Abdel-Hadi, Dina; Shams, Amany; Ahmad, Nermin et al.. (2012-11). «A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome» European journal of human genetics: EJHG 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. ISSN 1476-5438. PMID 22549407. PMC 3476705. (Noiz kontsultatua: 2024-03-10).
Cordovado, S. K.; Hendrix, M.; Greene, C. N.; Mochal, S.; Earley, M. C.; Farrell, P. M.; Kharrazi, M.; Hannon, W. H. et al.. (2012-02). «CFTR mutation analysis and haplotype associations in CF patients» Molecular Genetics and Metabolism 105 (2): 249–254. doi:10.1016/j.ymgme.2011.10.013. ISSN 1096-7206. PMID 22137130. PMC 3551260. (Noiz kontsultatua: 2024-03-10).
Lu, Yi-Fan; Mauger, David M.; Goldstein, David B.; Urban, Thomas J.; Weeks, Kevin M.; Bradrick, Shelton S.. (2015-11-04). «IFNL3 mRNA structure is remodeled by a functional non-coding polymorphism associated with hepatitis C virus clearance» Scientific Reports 5: 16037. doi:10.1038/srep16037. ISSN 2045-2322. PMID 26531896. PMC 4631997. (Noiz kontsultatua: 2024-03-10).
Altshuler, D.; Pollara, V. J.; Cowles, C. R.; Van Etten, W. J.; Baldwin, J.; Linton, L.; Lander, E. S.. (2000-09-28). «An SNP map of the human genome generated by reduced representation shotgun sequencing» Nature 407 (6803): 513–516. doi:10.1038/35035083. ISSN 0028-0836. PMID 11029002. (Noiz kontsultatua: 2024-03-10).
(Ingelesez) Telenti, Amalio; Pierce, Levi C. T.; Biggs, William H.; di Iulio, Julia; Wong, Emily H. M.; Fabani, Martin M.; Kirkness, Ewen F.; Moustafa, Ahmed et al.. (2016-10-18). «Deep sequencing of 10,000 human genomes» Proceedings of the National Academy of Sciences 113 (42): 11901–11906. doi:10.1073/pnas.1613365113. ISSN 0027-8424. PMID 27702888. PMC PMC5081584. (Noiz kontsultatua: 2024-03-10).
Tahira, Tomoko; Kukita, Yoji; Higasa, Koichiro; Okazaki, Yuko; Yoshinaga, Aki; Hayashi, Kenshi. (2009). «Estimation of SNP allele frequencies by SSCP analysis of pooled DNA» Methods in Molecular Biology (Clifton, N.J.) 578: 193–207. doi:10.1007/978-1-60327-411-1_12. ISSN 1940-6029. PMID 19768595. (Noiz kontsultatua: 2024-03-10).
«Home - SNP - NCBI» www.ncbi.nlm.nih.gov (Noiz kontsultatua: 2024-03-10).
(Ingelesez) «Clustered RefSNPs (rs) and Other Data Computed in House» SNP FAQ Archive [Internet] (National Center for Biotechnology Information (US)) 2014-02-18 (Noiz kontsultatua: 2024-03-10).
Ogino, Shuji; Gulley, Margaret L.; den Dunnen, Johan T.; Wilson, Robert B.. (2007-2). «Standard Mutation Nomenclature in Molecular Diagnostics» The Journal of molecular diagnostics : JMD 9 (1): 1–6. doi:10.2353/jmoldx.2007.060081. ISSN 1525-1578. PMID 17251329. PMC 1867422. (Noiz kontsultatua: 2024-03-10).
Morita, Akihiko; Nakayama, Tomohiro; Doba, Nobutaka; Hinohara, Shigeaki; Mizutani, Tomohiko; Soma, Masayoshi. (2007-06). «Genotyping of triallelic SNPs using TaqMan PCR» Molecular and Cellular Probes 21 (3): 171–176. doi:10.1016/j.mcp.2006.10.005. ISSN 0890-8508. PMID 17161935. (Noiz kontsultatua: 2024-03-10).
Prodi, D. A.; Drayna, D.; Forabosco, P.; Palmas, M. A.; Maestrale, G. B.; Piras, D.; Pirastu, M.; Angius, A.. (2004-10). «Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene» Chemical Senses 29 (8): 697–702. doi:10.1093/chemse/bjh074. ISSN 0379-864X. PMID 15466815. (Noiz kontsultatua: 2024-03-10).
Wolpin, Brian M.; Rizzato, Cosmeri; Kraft, Peter; Kooperberg, Charles; Petersen, Gloria M.; Wang, Zhaoming; Arslan, Alan A.; Beane-Freeman, Laura et al.. (2014-09). «Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer» Nature Genetics 46 (9): 994–1000. doi:10.1038/ng.3052. ISSN 1546-1718. PMID 25086665. PMC 4191666. (Noiz kontsultatua: 2024-03-10).

pubmed.ncbi.nlm.nih.gov

Spencer, Paige S.; Barral, José M.. (2012). «Genetic code redundancy and its influence on the encoded polypeptides» Computational and Structural Biotechnology Journal 1: e201204006. doi:10.5936/csbj.201204006. ISSN 2001-0370. PMID 24688635. PMC 3962081. (Noiz kontsultatua: 2024-03-10).
Chu, Duan; Wei, Lai. (2019-04-16). «Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation» BMC cancer 19 (1): 359. doi:10.1186/s12885-019-5572-x. ISSN 1471-2407. PMID 30991970. PMC 6469204. (Noiz kontsultatua: 2024-03-10).
Kimchi-Sarfaty, Chava; Oh, Jung Mi; Kim, In-Wha; Sauna, Zuben E.; Calcagno, Anna Maria; Ambudkar, Suresh V.; Gottesman, Michael M.. (2007-01-26). «A "silent" polymorphism in the MDR1 gene changes substrate specificity» Science (New York, N.Y.) 315 (5811): 525–528. doi:10.1126/science.1135308. ISSN 1095-9203. PMID 17185560. (Noiz kontsultatua: 2024-03-10).
Al-Haggar, Mohammad; Madej-Pilarczyk, Agnieszka; Kozlowski, Lukasz; Bujnicki, Janusz M.; Yahia, Sohier; Abdel-Hadi, Dina; Shams, Amany; Ahmad, Nermin et al.. (2012-11). «A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome» European journal of human genetics: EJHG 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. ISSN 1476-5438. PMID 22549407. PMC 3476705. (Noiz kontsultatua: 2024-03-10).
Cordovado, S. K.; Hendrix, M.; Greene, C. N.; Mochal, S.; Earley, M. C.; Farrell, P. M.; Kharrazi, M.; Hannon, W. H. et al.. (2012-02). «CFTR mutation analysis and haplotype associations in CF patients» Molecular Genetics and Metabolism 105 (2): 249–254. doi:10.1016/j.ymgme.2011.10.013. ISSN 1096-7206. PMID 22137130. PMC 3551260. (Noiz kontsultatua: 2024-03-10).
Altshuler, D.; Pollara, V. J.; Cowles, C. R.; Van Etten, W. J.; Baldwin, J.; Linton, L.; Lander, E. S.. (2000-09-28). «An SNP map of the human genome generated by reduced representation shotgun sequencing» Nature 407 (6803): 513–516. doi:10.1038/35035083. ISSN 0028-0836. PMID 11029002. (Noiz kontsultatua: 2024-03-10).
Tahira, Tomoko; Kukita, Yoji; Higasa, Koichiro; Okazaki, Yuko; Yoshinaga, Aki; Hayashi, Kenshi. (2009). «Estimation of SNP allele frequencies by SSCP analysis of pooled DNA» Methods in Molecular Biology (Clifton, N.J.) 578: 193–207. doi:10.1007/978-1-60327-411-1_12. ISSN 1940-6029. PMID 19768595. (Noiz kontsultatua: 2024-03-10).
Morita, Akihiko; Nakayama, Tomohiro; Doba, Nobutaka; Hinohara, Shigeaki; Mizutani, Tomohiko; Soma, Masayoshi. (2007-06). «Genotyping of triallelic SNPs using TaqMan PCR» Molecular and Cellular Probes 21 (3): 171–176. doi:10.1016/j.mcp.2006.10.005. ISSN 0890-8508. PMID 17161935. (Noiz kontsultatua: 2024-03-10).
Prodi, D. A.; Drayna, D.; Forabosco, P.; Palmas, M. A.; Maestrale, G. B.; Piras, D.; Pirastu, M.; Angius, A.. (2004-10). «Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene» Chemical Senses 29 (8): 697–702. doi:10.1093/chemse/bjh074. ISSN 0379-864X. PMID 15466815. (Noiz kontsultatua: 2024-03-10).
Wolpin, Brian M.; Rizzato, Cosmeri; Kraft, Peter; Kooperberg, Charles; Petersen, Gloria M.; Wang, Zhaoming; Arslan, Alan A.; Beane-Freeman, Laura et al.. (2014-09). «Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer» Nature Genetics 46 (9): 994–1000. doi:10.1038/ng.3052. ISSN 1546-1718. PMID 25086665. PMC 4191666. (Noiz kontsultatua: 2024-03-10).

pubmedcentral.nih.gov

Sherry, S. T.. (2001-01-01). «dbSNP: the NCBI database of genetic variation» Nucleic Acids Research 29 (1): 308–311. doi:10.1093/nar/29.1.308. ISSN 1362-4962. PMID 11125122. PMC PMC29783. (Noiz kontsultatua: 2024-03-10).
Spencer, Paige S.; Barral, José M.. (2012). «Genetic code redundancy and its influence on the encoded polypeptides» Computational and Structural Biotechnology Journal 1: e201204006. doi:10.5936/csbj.201204006. ISSN 2001-0370. PMID 24688635. PMC 3962081. (Noiz kontsultatua: 2024-03-10).
Chu, Duan; Wei, Lai. (2019-04-16). «Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation» BMC cancer 19 (1): 359. doi:10.1186/s12885-019-5572-x. ISSN 1471-2407. PMID 30991970. PMC 6469204. (Noiz kontsultatua: 2024-03-10).
Al-Haggar, Mohammad; Madej-Pilarczyk, Agnieszka; Kozlowski, Lukasz; Bujnicki, Janusz M.; Yahia, Sohier; Abdel-Hadi, Dina; Shams, Amany; Ahmad, Nermin et al.. (2012-11). «A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome» European journal of human genetics: EJHG 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. ISSN 1476-5438. PMID 22549407. PMC 3476705. (Noiz kontsultatua: 2024-03-10).
Cordovado, S. K.; Hendrix, M.; Greene, C. N.; Mochal, S.; Earley, M. C.; Farrell, P. M.; Kharrazi, M.; Hannon, W. H. et al.. (2012-02). «CFTR mutation analysis and haplotype associations in CF patients» Molecular Genetics and Metabolism 105 (2): 249–254. doi:10.1016/j.ymgme.2011.10.013. ISSN 1096-7206. PMID 22137130. PMC 3551260. (Noiz kontsultatua: 2024-03-10).
Lu, Yi-Fan; Mauger, David M.; Goldstein, David B.; Urban, Thomas J.; Weeks, Kevin M.; Bradrick, Shelton S.. (2015-11-04). «IFNL3 mRNA structure is remodeled by a functional non-coding polymorphism associated with hepatitis C virus clearance» Scientific Reports 5: 16037. doi:10.1038/srep16037. ISSN 2045-2322. PMID 26531896. PMC 4631997. (Noiz kontsultatua: 2024-03-10).
(Ingelesez) Telenti, Amalio; Pierce, Levi C. T.; Biggs, William H.; di Iulio, Julia; Wong, Emily H. M.; Fabani, Martin M.; Kirkness, Ewen F.; Moustafa, Ahmed et al.. (2016-10-18). «Deep sequencing of 10,000 human genomes» Proceedings of the National Academy of Sciences 113 (42): 11901–11906. doi:10.1073/pnas.1613365113. ISSN 0027-8424. PMID 27702888. PMC PMC5081584. (Noiz kontsultatua: 2024-03-10).
Ogino, Shuji; Gulley, Margaret L.; den Dunnen, Johan T.; Wilson, Robert B.. (2007-2). «Standard Mutation Nomenclature in Molecular Diagnostics» The Journal of molecular diagnostics : JMD 9 (1): 1–6. doi:10.2353/jmoldx.2007.060081. ISSN 1525-1578. PMID 17251329. PMC 1867422. (Noiz kontsultatua: 2024-03-10).
Wolpin, Brian M.; Rizzato, Cosmeri; Kraft, Peter; Kooperberg, Charles; Petersen, Gloria M.; Wang, Zhaoming; Arslan, Alan A.; Beane-Freeman, Laura et al.. (2014-09). «Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer» Nature Genetics 46 (9): 994–1000. doi:10.1038/ng.3052. ISSN 1546-1718. PMID 25086665. PMC 4191666. (Noiz kontsultatua: 2024-03-10).

pnas.org

(Ingelesez) Telenti, Amalio; Pierce, Levi C. T.; Biggs, William H.; di Iulio, Julia; Wong, Emily H. M.; Fabani, Martin M.; Kirkness, Ewen F.; Moustafa, Ahmed et al.. (2016-10-18). «Deep sequencing of 10,000 human genomes» Proceedings of the National Academy of Sciences 113 (42): 11901–11906. doi:10.1073/pnas.1613365113. ISSN 0027-8424. PMID 27702888. PMC PMC5081584. (Noiz kontsultatua: 2024-03-10).

snpedia.com

«SNPedia» www.snpedia.com (Noiz kontsultatua: 2024-03-10).

worldcat.org

Sherry, S. T.. (2001-01-01). «dbSNP: the NCBI database of genetic variation» Nucleic Acids Research 29 (1): 308–311. doi:10.1093/nar/29.1.308. ISSN 1362-4962. PMID 11125122. PMC PMC29783. (Noiz kontsultatua: 2024-03-10).
Spencer, Paige S.; Barral, José M.. (2012). «Genetic code redundancy and its influence on the encoded polypeptides» Computational and Structural Biotechnology Journal 1: e201204006. doi:10.5936/csbj.201204006. ISSN 2001-0370. PMID 24688635. PMC 3962081. (Noiz kontsultatua: 2024-03-10).
Chu, Duan; Wei, Lai. (2019-04-16). «Nonsynonymous, synonymous and nonsense mutations in human cancer-related genes undergo stronger purifying selections than expectation» BMC cancer 19 (1): 359. doi:10.1186/s12885-019-5572-x. ISSN 1471-2407. PMID 30991970. PMC 6469204. (Noiz kontsultatua: 2024-03-10).
Kimchi-Sarfaty, Chava; Oh, Jung Mi; Kim, In-Wha; Sauna, Zuben E.; Calcagno, Anna Maria; Ambudkar, Suresh V.; Gottesman, Michael M.. (2007-01-26). «A "silent" polymorphism in the MDR1 gene changes substrate specificity» Science (New York, N.Y.) 315 (5811): 525–528. doi:10.1126/science.1135308. ISSN 1095-9203. PMID 17185560. (Noiz kontsultatua: 2024-03-10).
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