Comparative genomic hybridization (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Comparative genomic hybridization" in English language version.

Last modified: 20:17:25, 29 August 2026 (UTC)

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2521nih.gov

5^th place

2016doi.org

2^nd place

77semanticscholar.org

15^th place

8^th place

32adsabs.harvard.edu

14^th place

9^th place

11nbn-resolving.de

1,834^th place

8,390^th place

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Kallioniemi A, Kallioniemi OP, Sudar DA, Rutovitz D, Gray JW, Waldman F, Pinkel D (1992). "Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors". Science. 258 (5083): 818–821. Bibcode:1992Sci...258..818K. doi:10.1126/science.1359641. PMID 1359641.
Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M (21 March 2006). "High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays". Proc Natl Acad Sci U S A. 103 (12): 4534–4539. Bibcode:2006PNAS..103.4534U. doi:10.1073/pnas.0511340103. PMC 1450206. PMID 16537408.

doi.org (Global: 2^nd place; English: 2^nd place)

Kallioniemi A, Kallioniemi OP, Sudar DA, Rutovitz D, Gray JW, Waldman F, Pinkel D (1992). "Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors". Science. 258 (5083): 818–821. Bibcode:1992Sci...258..818K. doi:10.1126/science.1359641. PMID 1359641.
du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T (1993). "Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization". Human Genetics. 90 (6): 590–610. doi:10.1007/bf00202476. PMID 8444465. S2CID 21440368.
Inazawa J, Inoue J, Imoto I (2004). "Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes". Cancer Science. 95 (7): 559–563. doi:10.1111/j.1349-7006.2004.tb02486.x. PMC 11158872. PMID 15245590. S2CID 33315320.
Pinkel D, Albertson DG (2005). "Array comparative genomic hybridization and its applications in cancer". Nat Genet. 37 (6s): 11–17. doi:10.1038/ng1569. PMID 15920524.
Ren H, Francis W, Boys A, Chueh AC, Wong N, La P, Wong LH, Ryan J, Slater HR, Choo KH (May 2005). "BAC-based PCR fragment microarray: high-resolution detection of chromosomal deletion and duplication breakpoints". Human Mutation. 25 (5): 476–82. doi:10.1002/humu.20164. PMID 15832308. S2CID 28030180.
Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M (21 March 2006). "High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays". Proc Natl Acad Sci U S A. 103 (12): 4534–4539. Bibcode:2006PNAS..103.4534U. doi:10.1073/pnas.0511340103. PMC 1450206. PMID 16537408.
Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, Smith J, Vetrie D, Gorman P, Tomlinson IP, Carter NP (2003). "DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones". Genes Chromosomes Cancer. 36 (4): 361–374. doi:10.1002/gcc.10155. PMID 12619160. S2CID 6929961.
Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, Jeffrey SS, Botstein D, Brown PO (1999). "Genome-wide analysis of DNA copy number changes using cDNA microarrays". Nat Genet. 23 (1): 41–46. doi:10.1038/12640. PMID 10471496. S2CID 997032.
Carvalho B, Ouwerkerk E, Meijer GA, Ylstra B (2004). "High resolution microarray comparative genomic hybridization analysis using spotted oligonucleotides". J Clin Pathol. 57 (6): 644–646. doi:10.1136/jcp.2003.013029. PMC 1770328. PMID 15166273.
Forozan F, Karhu R, Kononen J, Kallioniemi A, Kallioniemi OP (1997). "Genome screening by comparative genomic hybridization". Trends Genet. 13 (10): 405–409. doi:10.1016/s0168-9525(97)01244-4. PMID 9351342.
Levy B, Dunn TM, Kern JH, Hirschhorn K, Kardon NB (2002). "Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (Cri du Chat)". Am J Med Genet. 108 (3): 192–197. doi:10.1002/ajmg.10261. PMID 11891684.
Aprelikova O, Chen K, El Touny LH, Brignatz-Guittard C, Han J, Qiu T, Yang HH, Lee MP, Zhu M, Green JE (Apr 2016). "The epigenetic modifier JMJD6 is amplified in mammary tumors and cooperates with c-Myc to enhance cellular transformation, tumor progression, and metastasis". Clin Epigenetics. 8 (38): 38. doi:10.1186/s13148-016-0205-6. PMC 4831179. PMID 27081402.
Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EH, van Rijk A, Smeets D, van Ravenswaaij-Arts CM, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, Geurts, van Kessel A, Schoenmakers EF, Veltman JA (2003). "Array-based comparative genomic hybridization for the genome-wide detection of submicroscopic chromosomal abnormalities". Am J Hum Genet. 73 (6): 1261–1270. doi:10.1086/379977. PMC 1180392. PMID 14628292.
Fiorentino F (2012). "Array comparative genomic hybridization: its role in preimplantation genetic diagnosis". Current Opinion in Obstetrics and Gynecology. 24 (4): 203–209. doi:10.1097/gco.0b013e328355854d. PMID 22729095. S2CID 6484211.
Lee CN, Lin SY, Lin CH, Shih JC, Lin TH, Su YN (2012). "Clinical utility of array comparative genomic hybridization for prenatal diagnosis: a cohort study of 3171 pregnancies". BJOG: An International Journal of Obstetrics & Gynaecology. 119 (5): 614–625. doi:10.1111/j.1471-0528.2012.03279.x. PMID 22313859.
Shaw CJ, Stankiewicz P, Bien-Willner G, Bello SC, Shaw CA, Carrera M, Perez Jurado L, Estivill X, Lupski JR (2004). "Small marker chromosomes in two patients with segmental aneusomy for proximal 17p". Hum Genet. 115 (1): 1–7. doi:10.1007/s00439-004-1119-5. PMID 15098121. S2CID 1093845.

nbn-resolving.de (Global: 1,834^th place; English: 8,390^th place)

du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T (1993). "Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization". Human Genetics. 90 (6): 590–610. doi:10.1007/bf00202476. PMID 8444465. S2CID 21440368.

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Kallioniemi A, Kallioniemi OP, Sudar DA, Rutovitz D, Gray JW, Waldman F, Pinkel D (1992). "Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors". Science. 258 (5083): 818–821. Bibcode:1992Sci...258..818K. doi:10.1126/science.1359641. PMID 1359641.
du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T (1993). "Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization". Human Genetics. 90 (6): 590–610. doi:10.1007/bf00202476. PMID 8444465. S2CID 21440368.
Inazawa J, Inoue J, Imoto I (2004). "Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes". Cancer Science. 95 (7): 559–563. doi:10.1111/j.1349-7006.2004.tb02486.x. PMC 11158872. PMID 15245590. S2CID 33315320.
Pinkel D, Albertson DG (2005). "Array comparative genomic hybridization and its applications in cancer". Nat Genet. 37 (6s): 11–17. doi:10.1038/ng1569. PMID 15920524.
Ren H, Francis W, Boys A, Chueh AC, Wong N, La P, Wong LH, Ryan J, Slater HR, Choo KH (May 2005). "BAC-based PCR fragment microarray: high-resolution detection of chromosomal deletion and duplication breakpoints". Human Mutation. 25 (5): 476–82. doi:10.1002/humu.20164. PMID 15832308. S2CID 28030180.
Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M (21 March 2006). "High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays". Proc Natl Acad Sci U S A. 103 (12): 4534–4539. Bibcode:2006PNAS..103.4534U. doi:10.1073/pnas.0511340103. PMC 1450206. PMID 16537408.
Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, Smith J, Vetrie D, Gorman P, Tomlinson IP, Carter NP (2003). "DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones". Genes Chromosomes Cancer. 36 (4): 361–374. doi:10.1002/gcc.10155. PMID 12619160. S2CID 6929961.
Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, Jeffrey SS, Botstein D, Brown PO (1999). "Genome-wide analysis of DNA copy number changes using cDNA microarrays". Nat Genet. 23 (1): 41–46. doi:10.1038/12640. PMID 10471496. S2CID 997032.
Carvalho B, Ouwerkerk E, Meijer GA, Ylstra B (2004). "High resolution microarray comparative genomic hybridization analysis using spotted oligonucleotides". J Clin Pathol. 57 (6): 644–646. doi:10.1136/jcp.2003.013029. PMC 1770328. PMID 15166273.
Forozan F, Karhu R, Kononen J, Kallioniemi A, Kallioniemi OP (1997). "Genome screening by comparative genomic hybridization". Trends Genet. 13 (10): 405–409. doi:10.1016/s0168-9525(97)01244-4. PMID 9351342.
Levy B, Dunn TM, Kern JH, Hirschhorn K, Kardon NB (2002). "Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (Cri du Chat)". Am J Med Genet. 108 (3): 192–197. doi:10.1002/ajmg.10261. PMID 11891684.
Aprelikova O, Chen K, El Touny LH, Brignatz-Guittard C, Han J, Qiu T, Yang HH, Lee MP, Zhu M, Green JE (Apr 2016). "The epigenetic modifier JMJD6 is amplified in mammary tumors and cooperates with c-Myc to enhance cellular transformation, tumor progression, and metastasis". Clin Epigenetics. 8 (38): 38. doi:10.1186/s13148-016-0205-6. PMC 4831179. PMID 27081402.
Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EH, van Rijk A, Smeets D, van Ravenswaaij-Arts CM, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, Geurts, van Kessel A, Schoenmakers EF, Veltman JA (2003). "Array-based comparative genomic hybridization for the genome-wide detection of submicroscopic chromosomal abnormalities". Am J Hum Genet. 73 (6): 1261–1270. doi:10.1086/379977. PMC 1180392. PMID 14628292.
Fiorentino F (2012). "Array comparative genomic hybridization: its role in preimplantation genetic diagnosis". Current Opinion in Obstetrics and Gynecology. 24 (4): 203–209. doi:10.1097/gco.0b013e328355854d. PMID 22729095. S2CID 6484211.
Lee CN, Lin SY, Lin CH, Shih JC, Lin TH, Su YN (2012). "Clinical utility of array comparative genomic hybridization for prenatal diagnosis: a cohort study of 3171 pregnancies". BJOG: An International Journal of Obstetrics & Gynaecology. 119 (5): 614–625. doi:10.1111/j.1471-0528.2012.03279.x. PMID 22313859.
Shaw CJ, Stankiewicz P, Bien-Willner G, Bello SC, Shaw CA, Carrera M, Perez Jurado L, Estivill X, Lupski JR (2004). "Small marker chromosomes in two patients with segmental aneusomy for proximal 17p". Hum Genet. 115 (1): 1–7. doi:10.1007/s00439-004-1119-5. PMID 15098121. S2CID 1093845.

ncbi.nlm.nih.gov

Inazawa J, Inoue J, Imoto I (2004). "Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes". Cancer Science. 95 (7): 559–563. doi:10.1111/j.1349-7006.2004.tb02486.x. PMC 11158872. PMID 15245590. S2CID 33315320.
Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M (21 March 2006). "High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays". Proc Natl Acad Sci U S A. 103 (12): 4534–4539. Bibcode:2006PNAS..103.4534U. doi:10.1073/pnas.0511340103. PMC 1450206. PMID 16537408.
Carvalho B, Ouwerkerk E, Meijer GA, Ylstra B (2004). "High resolution microarray comparative genomic hybridization analysis using spotted oligonucleotides". J Clin Pathol. 57 (6): 644–646. doi:10.1136/jcp.2003.013029. PMC 1770328. PMID 15166273.
Aprelikova O, Chen K, El Touny LH, Brignatz-Guittard C, Han J, Qiu T, Yang HH, Lee MP, Zhu M, Green JE (Apr 2016). "The epigenetic modifier JMJD6 is amplified in mammary tumors and cooperates with c-Myc to enhance cellular transformation, tumor progression, and metastasis". Clin Epigenetics. 8 (38): 38. doi:10.1186/s13148-016-0205-6. PMC 4831179. PMID 27081402.
Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EH, van Rijk A, Smeets D, van Ravenswaaij-Arts CM, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, Geurts, van Kessel A, Schoenmakers EF, Veltman JA (2003). "Array-based comparative genomic hybridization for the genome-wide detection of submicroscopic chromosomal abnormalities". Am J Hum Genet. 73 (6): 1261–1270. doi:10.1086/379977. PMC 1180392. PMID 14628292.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T (1993). "Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization". Human Genetics. 90 (6): 590–610. doi:10.1007/bf00202476. PMID 8444465. S2CID 21440368.
Inazawa J, Inoue J, Imoto I (2004). "Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes". Cancer Science. 95 (7): 559–563. doi:10.1111/j.1349-7006.2004.tb02486.x. PMC 11158872. PMID 15245590. S2CID 33315320.
Ren H, Francis W, Boys A, Chueh AC, Wong N, La P, Wong LH, Ryan J, Slater HR, Choo KH (May 2005). "BAC-based PCR fragment microarray: high-resolution detection of chromosomal deletion and duplication breakpoints". Human Mutation. 25 (5): 476–82. doi:10.1002/humu.20164. PMID 15832308. S2CID 28030180.
Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, Smith J, Vetrie D, Gorman P, Tomlinson IP, Carter NP (2003). "DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones". Genes Chromosomes Cancer. 36 (4): 361–374. doi:10.1002/gcc.10155. PMID 12619160. S2CID 6929961.
Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, Jeffrey SS, Botstein D, Brown PO (1999). "Genome-wide analysis of DNA copy number changes using cDNA microarrays". Nat Genet. 23 (1): 41–46. doi:10.1038/12640. PMID 10471496. S2CID 997032.
Fiorentino F (2012). "Array comparative genomic hybridization: its role in preimplantation genetic diagnosis". Current Opinion in Obstetrics and Gynecology. 24 (4): 203–209. doi:10.1097/gco.0b013e328355854d. PMID 22729095. S2CID 6484211.
Shaw CJ, Stankiewicz P, Bien-Willner G, Bello SC, Shaw CA, Carrera M, Perez Jurado L, Estivill X, Lupski JR (2004). "Small marker chromosomes in two patients with segmental aneusomy for proximal 17p". Hum Genet. 115 (1): 1–7. doi:10.1007/s00439-004-1119-5. PMID 15098121. S2CID 1093845.

Comparative genomic hybridization (English Wikipedia)

adsabs.harvard.edu (Global: 14th place; English: 9th place)

ui.adsabs.harvard.edu

doi.org (Global: 2nd place; English: 2nd place)

nbn-resolving.de (Global: 1,834th place; English: 8,390th place)

nih.gov (Global: 5th place; English: 5th place)