Locus heterogeneity (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Locus heterogeneity" in English language version.

refsWebsite

Global rank English rank

19nih.gov

4^th place

12doi.org

2^nd place

4semanticscholar.org

11^th place

8^th place

1cancer.gov

1,684^th place

1,350^th place

1harvard.edu

18^th place

17^th place

1cshlp.org

low place

1worldcat.org

5^th place

1thelancet.com

2,393^rd place

3,174^th place

1uth.edu

low place

cancer.gov

"NCI Dictionary of Genetics Terms". National Cancer Institute. 2012-07-20. Retrieved 2019-11-27.

cshlp.org

genome.cshlp.org

Keats, Bronya J. B.; Berlin, Charles I. (1999-01-01). "Genomics and Hearing Impairment". Genome Research. 9 (1): 7–16. doi:10.1101/gr.9.1.7. ISSN 1088-9051. PMID 9927480.

doi.org

Keith BP, Robertson DL, Hentges KE (2014-12-09). "Locus heterogeneity disease genes encode proteins with high interconnectivity in the human protein interaction network". Frontiers in Genetics. 5: 434. doi:10.3389/fgene.2014.00434. PMC 4260505. PMID 25538735.
Ackermann M (August 2015). "A functional perspective on phenotypic heterogeneity in microorganisms". Nature Reviews. Microbiology. 13 (8): 497–508. doi:10.1038/nrmicro3491. PMID 26145732. S2CID 29846214.
Daiger SP, Sullivan LS, Bowne SJ (August 2013). "Genes and mutations causing retinitis pigmentosa". Clinical Genetics. 84 (2): 132–41. doi:10.1111/cge.12203. PMC 3856531. PMID 23701314.
Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, et al. (September 1990). "Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease". The Journal of Clinical Investigation. 86 (3): 993–9. doi:10.1172/JCI114802. PMC 296820. PMID 1975599.
Van Dijk FS, Sillence DO (June 2014). "Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment". American Journal of Medical Genetics. Part A. 164A (6): 1470–81. doi:10.1002/ajmg.a.36545. PMC 4314691. PMID 24715559.
Goldstein JL, Dana SE, Brunschede GY, Brown MS (March 1975). "Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor". Proceedings of the National Academy of Sciences of the United States of America. 72 (3): 1092–6. Bibcode:1975PNAS...72.1092G. doi:10.1073/pnas.72.3.1092. PMC 432472. PMID 236556.
Keats, Bronya J. B.; Berlin, Charles I. (1999-01-01). "Genomics and Hearing Impairment". Genome Research. 9 (1): 7–16. doi:10.1101/gr.9.1.7. ISSN 1088-9051. PMID 9927480.
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, et al. (September 2015). "Challenges and solutions for gene identification in the presence of familial locus heterogeneity". European Journal of Human Genetics. 23 (9): 1207–15. doi:10.1038/ejhg.2014.266. PMC 4538203. PMID 25491636.
Wang D, Huang J (May 2006). "Detecting linkage disequilibrium in the presence of locus heterogeneity". Annals of Human Genetics. 70 (Pt 3): 397–409. doi:10.1111/j.1529-8817.2005.00229.x. PMID 16674561. S2CID 25856694.
Pal DK, Greenberg DA (2002). "Evaluating genetic heterogeneity in complex disorders". Human Heredity. 53 (4): 216–26. doi:10.1159/000066195. PMID 12435885. S2CID 46285173.
Hartong DT, Berson EL, Dryja TP (November 2006). "Retinitis pigmentosa". Lancet. 368 (9549): 1795–809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430. S2CID 24950783.
Ferrari S, Di Iorio E, Barbaro V, Ponzin D, Sorrentino FS, Parmeggiani F (June 2011). "Retinitis pigmentosa: genes and disease mechanisms". Current Genomics. 12 (4): 238–49. doi:10.2174/138920211795860107. PMC 3131731. PMID 22131869.

harvard.edu

ui.adsabs.harvard.edu

Goldstein JL, Dana SE, Brunschede GY, Brown MS (March 1975). "Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor". Proceedings of the National Academy of Sciences of the United States of America. 72 (3): 1092–6. Bibcode:1975PNAS...72.1092G. doi:10.1073/pnas.72.3.1092. PMC 432472. PMID 236556.

nih.gov

pubmed.ncbi.nlm.nih.gov

Keith BP, Robertson DL, Hentges KE (2014-12-09). "Locus heterogeneity disease genes encode proteins with high interconnectivity in the human protein interaction network". Frontiers in Genetics. 5: 434. doi:10.3389/fgene.2014.00434. PMC 4260505. PMID 25538735.
Ackermann M (August 2015). "A functional perspective on phenotypic heterogeneity in microorganisms". Nature Reviews. Microbiology. 13 (8): 497–508. doi:10.1038/nrmicro3491. PMID 26145732. S2CID 29846214.
Daiger SP, Sullivan LS, Bowne SJ (August 2013). "Genes and mutations causing retinitis pigmentosa". Clinical Genetics. 84 (2): 132–41. doi:10.1111/cge.12203. PMC 3856531. PMID 23701314.
Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, et al. (September 1990). "Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease". The Journal of Clinical Investigation. 86 (3): 993–9. doi:10.1172/JCI114802. PMC 296820. PMID 1975599.
Van Dijk FS, Sillence DO (June 2014). "Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment". American Journal of Medical Genetics. Part A. 164A (6): 1470–81. doi:10.1002/ajmg.a.36545. PMC 4314691. PMID 24715559.
Goldstein JL, Dana SE, Brunschede GY, Brown MS (March 1975). "Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor". Proceedings of the National Academy of Sciences of the United States of America. 72 (3): 1092–6. Bibcode:1975PNAS...72.1092G. doi:10.1073/pnas.72.3.1092. PMC 432472. PMID 236556.
Keats, Bronya J. B.; Berlin, Charles I. (1999-01-01). "Genomics and Hearing Impairment". Genome Research. 9 (1): 7–16. doi:10.1101/gr.9.1.7. ISSN 1088-9051. PMID 9927480.
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, et al. (September 2015). "Challenges and solutions for gene identification in the presence of familial locus heterogeneity". European Journal of Human Genetics. 23 (9): 1207–15. doi:10.1038/ejhg.2014.266. PMC 4538203. PMID 25491636.
Wang D, Huang J (May 2006). "Detecting linkage disequilibrium in the presence of locus heterogeneity". Annals of Human Genetics. 70 (Pt 3): 397–409. doi:10.1111/j.1529-8817.2005.00229.x. PMID 16674561. S2CID 25856694.
Pal DK, Greenberg DA (2002). "Evaluating genetic heterogeneity in complex disorders". Human Heredity. 53 (4): 216–26. doi:10.1159/000066195. PMID 12435885. S2CID 46285173.
Hartong DT, Berson EL, Dryja TP (November 2006). "Retinitis pigmentosa". Lancet. 368 (9549): 1795–809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430. S2CID 24950783.
Ferrari S, Di Iorio E, Barbaro V, Ponzin D, Sorrentino FS, Parmeggiani F (June 2011). "Retinitis pigmentosa: genes and disease mechanisms". Current Genomics. 12 (4): 238–49. doi:10.2174/138920211795860107. PMC 3131731. PMID 22131869.

ncbi.nlm.nih.gov

Keith BP, Robertson DL, Hentges KE (2014-12-09). "Locus heterogeneity disease genes encode proteins with high interconnectivity in the human protein interaction network". Frontiers in Genetics. 5: 434. doi:10.3389/fgene.2014.00434. PMC 4260505. PMID 25538735.
Daiger SP, Sullivan LS, Bowne SJ (August 2013). "Genes and mutations causing retinitis pigmentosa". Clinical Genetics. 84 (2): 132–41. doi:10.1111/cge.12203. PMC 3856531. PMID 23701314.
Solomon SD, Jarcho JA, McKenna W, Geisterfer-Lowrance A, Germain R, Salerni R, et al. (September 1990). "Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease". The Journal of Clinical Investigation. 86 (3): 993–9. doi:10.1172/JCI114802. PMC 296820. PMID 1975599.
Van Dijk FS, Sillence DO (June 2014). "Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment". American Journal of Medical Genetics. Part A. 164A (6): 1470–81. doi:10.1002/ajmg.a.36545. PMC 4314691. PMID 24715559.
Goldstein JL, Dana SE, Brunschede GY, Brown MS (March 1975). "Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor". Proceedings of the National Academy of Sciences of the United States of America. 72 (3): 1092–6. Bibcode:1975PNAS...72.1092G. doi:10.1073/pnas.72.3.1092. PMC 432472. PMID 236556.
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, et al. (September 2015). "Challenges and solutions for gene identification in the presence of familial locus heterogeneity". European Journal of Human Genetics. 23 (9): 1207–15. doi:10.1038/ejhg.2014.266. PMC 4538203. PMID 25491636.
Ferrari S, Di Iorio E, Barbaro V, Ponzin D, Sorrentino FS, Parmeggiani F (June 2011). "Retinitis pigmentosa: genes and disease mechanisms". Current Genomics. 12 (4): 238–49. doi:10.2174/138920211795860107. PMC 3131731. PMID 22131869.

semanticscholar.org

api.semanticscholar.org

Ackermann M (August 2015). "A functional perspective on phenotypic heterogeneity in microorganisms". Nature Reviews. Microbiology. 13 (8): 497–508. doi:10.1038/nrmicro3491. PMID 26145732. S2CID 29846214.
Wang D, Huang J (May 2006). "Detecting linkage disequilibrium in the presence of locus heterogeneity". Annals of Human Genetics. 70 (Pt 3): 397–409. doi:10.1111/j.1529-8817.2005.00229.x. PMID 16674561. S2CID 25856694.
Pal DK, Greenberg DA (2002). "Evaluating genetic heterogeneity in complex disorders". Human Heredity. 53 (4): 216–26. doi:10.1159/000066195. PMID 12435885. S2CID 46285173.
Hartong DT, Berson EL, Dryja TP (November 2006). "Retinitis pigmentosa". Lancet. 368 (9549): 1795–809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430. S2CID 24950783.

thelancet.com

Hartong DT, Berson EL, Dryja TP (November 2006). "Retinitis pigmentosa". Lancet. 368 (9549): 1795–809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430. S2CID 24950783.

uth.edu

sph.uth.edu

"RetNet: Summaries". sph.uth.edu. Retrieved 2019-11-27.

worldcat.org

search.worldcat.org

Keats, Bronya J. B.; Berlin, Charles I. (1999-01-01). "Genomics and Hearing Impairment". Genome Research. 9 (1): 7–16. doi:10.1101/gr.9.1.7. ISSN 1088-9051. PMID 9927480.