8p23.1 duplication syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "8p23.1 duplication syndrome" in English language version.

refsWebsite

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10nih.gov

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7doi.org

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2semanticscholar.org

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doi.org

Barber JC, Bunyan D, Curtis M, et al. (2010). "8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families". Mol Cytogenet. 3: 3. doi:10.1186/1755-8166-3-3. PMC 2846957. PMID 20167067.
Barber JC, Maloney V, Hollox EJ, et al. (October 2005). "Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level". Eur. J. Hum. Genet. 13 (10): 1131–6. doi:10.1038/sj.ejhg.5201475. PMID 16077733.
Barber JC, Maloney VK, Huang S, et al. (January 2008). "8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH". Eur. J. Hum. Genet. 16 (1): 18–27. doi:10.1038/sj.ejhg.5201932. PMID 17940555. S2CID 11077778.
Wat MJ, Shchelochkov OA, Holder AM, et al. (August 2009). "Chromosome 8p23.1 Deletions as a Cause of Complex Congenital Heart Defects and Diaphragmatic Hernia". Am. J. Med. Genet. A. 149A (8): 1661–77. doi:10.1002/ajmg.a.32896. PMC 2765374. PMID 19606479.
Páez MT, Yamamoto T, Hayashi K, et al. (May 2008). "Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits". Am. J. Med. Genet. A. 146A (9): 1158–65. doi:10.1002/ajmg.a.32205. PMID 18393291. S2CID 205309084.
Hollox EJ, Barber JC, Brookes AJ, Armour JA (2008). "Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1". Genome Res. 18 (11): 1686–97. doi:10.1101/gr.080945.108. PMID 18974263.
Fellermann K, Stange DE, Schaeffeler E, Schmalzl H, Wehkamp J, Bevins CL, Reinisch W, Teml A, Schwab M, Lichter P, Radlwimmer B, Stange EF (2006). "A Chromosome 8 Gene-Cluster Polymorphism with Low Human Beta-Defensin 2 Gene Copy Number Predisposes to Crohn Disease of the Colon". Am J Hum Genet. 79 (3): 439–48. doi:10.1086/505915. PMC 1559531. PMID 16909382.

nih.gov

pubmed.ncbi.nlm.nih.gov

Barber JC, Bunyan D, Curtis M, et al. (2010). "8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families". Mol Cytogenet. 3: 3. doi:10.1186/1755-8166-3-3. PMC 2846957. PMID 20167067.
Barber JC, Maloney V, Hollox EJ, et al. (October 2005). "Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level". Eur. J. Hum. Genet. 13 (10): 1131–6. doi:10.1038/sj.ejhg.5201475. PMID 16077733.
Barber JC, Maloney VK, Huang S, et al. (January 2008). "8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH". Eur. J. Hum. Genet. 16 (1): 18–27. doi:10.1038/sj.ejhg.5201932. PMID 17940555. S2CID 11077778.
Wat MJ, Shchelochkov OA, Holder AM, et al. (August 2009). "Chromosome 8p23.1 Deletions as a Cause of Complex Congenital Heart Defects and Diaphragmatic Hernia". Am. J. Med. Genet. A. 149A (8): 1661–77. doi:10.1002/ajmg.a.32896. PMC 2765374. PMID 19606479.
Páez MT, Yamamoto T, Hayashi K, et al. (May 2008). "Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits". Am. J. Med. Genet. A. 146A (9): 1158–65. doi:10.1002/ajmg.a.32205. PMID 18393291. S2CID 205309084.
Hollox EJ, Barber JC, Brookes AJ, Armour JA (2008). "Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1". Genome Res. 18 (11): 1686–97. doi:10.1101/gr.080945.108. PMID 18974263.
Fellermann K, Stange DE, Schaeffeler E, Schmalzl H, Wehkamp J, Bevins CL, Reinisch W, Teml A, Schwab M, Lichter P, Radlwimmer B, Stange EF (2006). "A Chromosome 8 Gene-Cluster Polymorphism with Low Human Beta-Defensin 2 Gene Copy Number Predisposes to Crohn Disease of the Colon". Am J Hum Genet. 79 (3): 439–48. doi:10.1086/505915. PMC 1559531. PMID 16909382.

ncbi.nlm.nih.gov

Barber JC, Bunyan D, Curtis M, et al. (2010). "8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families". Mol Cytogenet. 3: 3. doi:10.1186/1755-8166-3-3. PMC 2846957. PMID 20167067.
Wat MJ, Shchelochkov OA, Holder AM, et al. (August 2009). "Chromosome 8p23.1 Deletions as a Cause of Complex Congenital Heart Defects and Diaphragmatic Hernia". Am. J. Med. Genet. A. 149A (8): 1661–77. doi:10.1002/ajmg.a.32896. PMC 2765374. PMID 19606479.
Fellermann K, Stange DE, Schaeffeler E, Schmalzl H, Wehkamp J, Bevins CL, Reinisch W, Teml A, Schwab M, Lichter P, Radlwimmer B, Stange EF (2006). "A Chromosome 8 Gene-Cluster Polymorphism with Low Human Beta-Defensin 2 Gene Copy Number Predisposes to Crohn Disease of the Colon". Am J Hum Genet. 79 (3): 439–48. doi:10.1086/505915. PMC 1559531. PMID 16909382.

semanticscholar.org

api.semanticscholar.org

Barber JC, Maloney VK, Huang S, et al. (January 2008). "8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH". Eur. J. Hum. Genet. 16 (1): 18–27. doi:10.1038/sj.ejhg.5201932. PMID 17940555. S2CID 11077778.
Páez MT, Yamamoto T, Hayashi K, et al. (May 2008). "Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits". Am. J. Med. Genet. A. 146A (9): 1158–65. doi:10.1002/ajmg.a.32205. PMID 18393291. S2CID 205309084.