Carolyn J. Brown (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Carolyn J. Brown" in English language version.

refsWebsite

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23nih.gov

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16doi.org

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5semanticscholar.org

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3harvard.edu

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doi.org

Brown, Carolyn J.; Ballabio, Andrea; Rupert, James L.; Lafreniere, Ronald G.; Grompe, Markus; Tonlorenzi, Rossana; Willard, Huntington F. (1991). "A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome". Nature. 349 (6304): 38–44. Bibcode:1991Natur.349...38B. doi:10.1038/349038a0. PMID 1985261. S2CID 4332325.
Brown, Carolyn J.; Lafreniere, Ronald G.; Powers, Vicki E.; Sebastio, Gianfranco; Ballabio, Andrea; Pettigrew, Anjana L.; Ledbetter, David H.; Levy, Elaine; Craig, Ian W.; Willard, Huntington F. (1991). "Localization of the X inactivation centre on the human X chromosome in Xq13". Nature. 349 (6304): 82–84. Bibcode:1991Natur.349...82B. doi:10.1038/349082a0. PMID 1985270. S2CID 4360783.
Willard, Huntington F. (2010). "2009 William Allan Award Address: Life in the Sandbox: Unfinished Business". The American Journal of Human Genetics. 86 (3): 318–327. doi:10.1016/j.ajhg.2010.01.037. PMC 2833390.
Yen, Z. C.; Meyer, I. M.; Karalic, S.; Brown, C. J. (2007). "A cross-species comparison of X-chromosome inactivation in Eutheria". Genomics. 90 (4): 453–63. doi:10.1016/j.ygeno.2007.07.002. PMID 17728098.
Chang, S. C.; Brown, C. J. (2010). "Identification of regulatory elements flanking human XIST reveals species differences". BMC Molecular Biology. 11: 20. doi:10.1186/1471-2199-11-20. PMC 2841178. PMID 20211024.
Kutsche, R.; Brown, C. J. (2000). "Determination of X-chromosome inactivation status using X-linked expressed polymorphisms identified by database searching". Genomics. 65 (1): 9–15. doi:10.1006/geno.2000.6153. PMID 10777660.
Cotton, A. M.; Lam, L.; Affleck, J. G.; Wilson, I. M.; Peñaherrera, M. S.; McFadden, D. E.; Kobor, M. S.; Lam, W. L.; Robinson, W. P.; Brown, C. J. (2011). "Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation". Human Genetics. 130 (2): 187–201. doi:10.1007/s00439-011-1007-8. PMC 3132437. PMID 21597963.
Cotton, A. M.; Ge, B.; Light, N.; Adoue, V.; Pastinen, T.; Brown, C. J. (2013). "Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome". Genome Biology. 14 (11): R122. doi:10.1186/gb-2013-14-11-r122. PMC 4053723. PMID 24176135.
Cotton, A. M.; Price, E. M.; Jones, M. J.; Balaton, B. P.; Kobor, M. S.; Brown, C. J. (2015). "Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation". Human Molecular Genetics. 24 (6): 1528–39. doi:10.1093/hmg/ddu564. PMC 4381753. PMID 25381334.
Tinker, A. V.; Brown, C. J. (1998). "Induction of XIST expression from the human active X chromosome in mouse/human somatic cell hybrids by DNA demethylation". Nucleic Acids Research. 26 (12): 2935–40. doi:10.1093/nar/26.12.2935. PMC 147638. PMID 9611238.
Dawson, A. J.; Wickstrom, D. E.; Riordan, D.; Cardwell, S.; Casey, R.; Baldry, S.; Brown, C. (2004). "A unique patient with an Ullrich-Turner syndrome variant and mosaicism for a tiny r(X) and a partial proximal duplication 1q". American Journal of Medical Genetics. Part A. 124A (3): 303–6. doi:10.1002/ajmg.a.20302. PMID 14708105. S2CID 13408738.
Gibb, E. A.; Vucic, E. A.; Enfield, K. S.; Stewart, G. L.; Lonergan, K. M.; Kennett, J. Y.; Becker-Santos, D. D.; MacAulay, C. E.; Lam, S.; Brown, C. J.; Lam, W. L. (2011). "Human cancer long non-coding RNA transcriptomes". PLOS ONE. 6 (10): e25915. Bibcode:2011PLoSO...625915G. doi:10.1371/journal.pone.0025915. PMC 3185064. PMID 21991387.
Cheung, K. J.; Johnson, N. A.; Affleck, J. G.; Severson, T.; Steidl, C.; Ben-Neriah, S.; Schein, J.; Morin, R. D.; Moore, R.; Shah, S. P.; Qian, H.; Paul, J. E.; Telenius, A.; Relander, T.; Lam, W.; Savage, K.; Connors, J. M.; Brown, C.; Marra, M. A.; Gascoyne, R. D.; Horsman, D. E. (2010). "Acquired TNFRSF14 mutations in follicular lymphoma are associated with worse prognosis". Cancer Research. 70 (22): 9166–74. doi:10.1158/0008-5472.CAN-10-2460. PMID 20884631.
Johnson, N. A.; Al-Tourah, A.; Brown, C. J.; Connors, J. M.; Gascoyne, R. D.; Horsman, D. E. (2008). "Prognostic significance of secondary cytogenetic alterations in follicular lymphomas". Genes, Chromosomes & Cancer. 47 (12): 1038–48. doi:10.1002/gcc.20606. PMID 18720523. S2CID 20432234.
Hatakeyama, C.; Anderson, C. L.; Beever, C. L.; Peñaherrera, M. S.; Brown, C. J.; Robinson, W. P. (2004). "The dynamics of X-inactivation skewing as women age". Clinical Genetics. 66 (4): 327–32. doi:10.1111/j.1399-0004.2004.00310.x. PMID 15355435. S2CID 23931974.
Beever, C. L.; Stephenson, M. D.; Peñaherrera, M. S.; Jiang, R. H.; Kalousek, D. K.; Hayden, M.; Field, L.; Brown, C. J.; Robinson, W. P. (2003). "Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies". American Journal of Human Genetics. 72 (2): 399–407. doi:10.1086/346119. PMC 379232. PMID 12497247.

harvard.edu

ui.adsabs.harvard.edu

Brown, Carolyn J.; Ballabio, Andrea; Rupert, James L.; Lafreniere, Ronald G.; Grompe, Markus; Tonlorenzi, Rossana; Willard, Huntington F. (1991). "A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome". Nature. 349 (6304): 38–44. Bibcode:1991Natur.349...38B. doi:10.1038/349038a0. PMID 1985261. S2CID 4332325.
Brown, Carolyn J.; Lafreniere, Ronald G.; Powers, Vicki E.; Sebastio, Gianfranco; Ballabio, Andrea; Pettigrew, Anjana L.; Ledbetter, David H.; Levy, Elaine; Craig, Ian W.; Willard, Huntington F. (1991). "Localization of the X inactivation centre on the human X chromosome in Xq13". Nature. 349 (6304): 82–84. Bibcode:1991Natur.349...82B. doi:10.1038/349082a0. PMID 1985270. S2CID 4360783.
Gibb, E. A.; Vucic, E. A.; Enfield, K. S.; Stewart, G. L.; Lonergan, K. M.; Kennett, J. Y.; Becker-Santos, D. D.; MacAulay, C. E.; Lam, S.; Brown, C. J.; Lam, W. L. (2011). "Human cancer long non-coding RNA transcriptomes". PLOS ONE. 6 (10): e25915. Bibcode:2011PLoSO...625915G. doi:10.1371/journal.pone.0025915. PMC 3185064. PMID 21991387.

nih.gov

pubmed.ncbi.nlm.nih.gov

Brown, Carolyn J.; Ballabio, Andrea; Rupert, James L.; Lafreniere, Ronald G.; Grompe, Markus; Tonlorenzi, Rossana; Willard, Huntington F. (1991). "A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome". Nature. 349 (6304): 38–44. Bibcode:1991Natur.349...38B. doi:10.1038/349038a0. PMID 1985261. S2CID 4332325.
Brown, Carolyn J.; Lafreniere, Ronald G.; Powers, Vicki E.; Sebastio, Gianfranco; Ballabio, Andrea; Pettigrew, Anjana L.; Ledbetter, David H.; Levy, Elaine; Craig, Ian W.; Willard, Huntington F. (1991). "Localization of the X inactivation centre on the human X chromosome in Xq13". Nature. 349 (6304): 82–84. Bibcode:1991Natur.349...82B. doi:10.1038/349082a0. PMID 1985270. S2CID 4360783.
Yen, Z. C.; Meyer, I. M.; Karalic, S.; Brown, C. J. (2007). "A cross-species comparison of X-chromosome inactivation in Eutheria". Genomics. 90 (4): 453–63. doi:10.1016/j.ygeno.2007.07.002. PMID 17728098.
Chang, S. C.; Brown, C. J. (2010). "Identification of regulatory elements flanking human XIST reveals species differences". BMC Molecular Biology. 11: 20. doi:10.1186/1471-2199-11-20. PMC 2841178. PMID 20211024.
Kutsche, R.; Brown, C. J. (2000). "Determination of X-chromosome inactivation status using X-linked expressed polymorphisms identified by database searching". Genomics. 65 (1): 9–15. doi:10.1006/geno.2000.6153. PMID 10777660.
Cotton, A. M.; Lam, L.; Affleck, J. G.; Wilson, I. M.; Peñaherrera, M. S.; McFadden, D. E.; Kobor, M. S.; Lam, W. L.; Robinson, W. P.; Brown, C. J. (2011). "Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation". Human Genetics. 130 (2): 187–201. doi:10.1007/s00439-011-1007-8. PMC 3132437. PMID 21597963.
Cotton, A. M.; Ge, B.; Light, N.; Adoue, V.; Pastinen, T.; Brown, C. J. (2013). "Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome". Genome Biology. 14 (11): R122. doi:10.1186/gb-2013-14-11-r122. PMC 4053723. PMID 24176135.
Cotton, A. M.; Price, E. M.; Jones, M. J.; Balaton, B. P.; Kobor, M. S.; Brown, C. J. (2015). "Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation". Human Molecular Genetics. 24 (6): 1528–39. doi:10.1093/hmg/ddu564. PMC 4381753. PMID 25381334.
Tinker, A. V.; Brown, C. J. (1998). "Induction of XIST expression from the human active X chromosome in mouse/human somatic cell hybrids by DNA demethylation". Nucleic Acids Research. 26 (12): 2935–40. doi:10.1093/nar/26.12.2935. PMC 147638. PMID 9611238.
Dawson, A. J.; Wickstrom, D. E.; Riordan, D.; Cardwell, S.; Casey, R.; Baldry, S.; Brown, C. (2004). "A unique patient with an Ullrich-Turner syndrome variant and mosaicism for a tiny r(X) and a partial proximal duplication 1q". American Journal of Medical Genetics. Part A. 124A (3): 303–6. doi:10.1002/ajmg.a.20302. PMID 14708105. S2CID 13408738.
Gibb, E. A.; Vucic, E. A.; Enfield, K. S.; Stewart, G. L.; Lonergan, K. M.; Kennett, J. Y.; Becker-Santos, D. D.; MacAulay, C. E.; Lam, S.; Brown, C. J.; Lam, W. L. (2011). "Human cancer long non-coding RNA transcriptomes". PLOS ONE. 6 (10): e25915. Bibcode:2011PLoSO...625915G. doi:10.1371/journal.pone.0025915. PMC 3185064. PMID 21991387.
Cheung, K. J.; Johnson, N. A.; Affleck, J. G.; Severson, T.; Steidl, C.; Ben-Neriah, S.; Schein, J.; Morin, R. D.; Moore, R.; Shah, S. P.; Qian, H.; Paul, J. E.; Telenius, A.; Relander, T.; Lam, W.; Savage, K.; Connors, J. M.; Brown, C.; Marra, M. A.; Gascoyne, R. D.; Horsman, D. E. (2010). "Acquired TNFRSF14 mutations in follicular lymphoma are associated with worse prognosis". Cancer Research. 70 (22): 9166–74. doi:10.1158/0008-5472.CAN-10-2460. PMID 20884631.
Johnson, N. A.; Al-Tourah, A.; Brown, C. J.; Connors, J. M.; Gascoyne, R. D.; Horsman, D. E. (2008). "Prognostic significance of secondary cytogenetic alterations in follicular lymphomas". Genes, Chromosomes & Cancer. 47 (12): 1038–48. doi:10.1002/gcc.20606. PMID 18720523. S2CID 20432234.
Hatakeyama, C.; Anderson, C. L.; Beever, C. L.; Peñaherrera, M. S.; Brown, C. J.; Robinson, W. P. (2004). "The dynamics of X-inactivation skewing as women age". Clinical Genetics. 66 (4): 327–32. doi:10.1111/j.1399-0004.2004.00310.x. PMID 15355435. S2CID 23931974.
Beever, C. L.; Stephenson, M. D.; Peñaherrera, M. S.; Jiang, R. H.; Kalousek, D. K.; Hayden, M.; Field, L.; Brown, C. J.; Robinson, W. P. (2003). "Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies". American Journal of Human Genetics. 72 (2): 399–407. doi:10.1086/346119. PMC 379232. PMID 12497247.

ncbi.nlm.nih.gov

Willard, Huntington F. (2010). "2009 William Allan Award Address: Life in the Sandbox: Unfinished Business". The American Journal of Human Genetics. 86 (3): 318–327. doi:10.1016/j.ajhg.2010.01.037. PMC 2833390.
Chang, S. C.; Brown, C. J. (2010). "Identification of regulatory elements flanking human XIST reveals species differences". BMC Molecular Biology. 11: 20. doi:10.1186/1471-2199-11-20. PMC 2841178. PMID 20211024.
Cotton, A. M.; Lam, L.; Affleck, J. G.; Wilson, I. M.; Peñaherrera, M. S.; McFadden, D. E.; Kobor, M. S.; Lam, W. L.; Robinson, W. P.; Brown, C. J. (2011). "Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation". Human Genetics. 130 (2): 187–201. doi:10.1007/s00439-011-1007-8. PMC 3132437. PMID 21597963.
Cotton, A. M.; Ge, B.; Light, N.; Adoue, V.; Pastinen, T.; Brown, C. J. (2013). "Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome". Genome Biology. 14 (11): R122. doi:10.1186/gb-2013-14-11-r122. PMC 4053723. PMID 24176135.
Cotton, A. M.; Price, E. M.; Jones, M. J.; Balaton, B. P.; Kobor, M. S.; Brown, C. J. (2015). "Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation". Human Molecular Genetics. 24 (6): 1528–39. doi:10.1093/hmg/ddu564. PMC 4381753. PMID 25381334.
Tinker, A. V.; Brown, C. J. (1998). "Induction of XIST expression from the human active X chromosome in mouse/human somatic cell hybrids by DNA demethylation". Nucleic Acids Research. 26 (12): 2935–40. doi:10.1093/nar/26.12.2935. PMC 147638. PMID 9611238.
Gibb, E. A.; Vucic, E. A.; Enfield, K. S.; Stewart, G. L.; Lonergan, K. M.; Kennett, J. Y.; Becker-Santos, D. D.; MacAulay, C. E.; Lam, S.; Brown, C. J.; Lam, W. L. (2011). "Human cancer long non-coding RNA transcriptomes". PLOS ONE. 6 (10): e25915. Bibcode:2011PLoSO...625915G. doi:10.1371/journal.pone.0025915. PMC 3185064. PMID 21991387.
Beever, C. L.; Stephenson, M. D.; Peñaherrera, M. S.; Jiang, R. H.; Kalousek, D. K.; Hayden, M.; Field, L.; Brown, C. J.; Robinson, W. P. (2003). "Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies". American Journal of Human Genetics. 72 (2): 399–407. doi:10.1086/346119. PMC 379232. PMID 12497247.

semanticscholar.org

api.semanticscholar.org

Brown, Carolyn J.; Ballabio, Andrea; Rupert, James L.; Lafreniere, Ronald G.; Grompe, Markus; Tonlorenzi, Rossana; Willard, Huntington F. (1991). "A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome". Nature. 349 (6304): 38–44. Bibcode:1991Natur.349...38B. doi:10.1038/349038a0. PMID 1985261. S2CID 4332325.
Brown, Carolyn J.; Lafreniere, Ronald G.; Powers, Vicki E.; Sebastio, Gianfranco; Ballabio, Andrea; Pettigrew, Anjana L.; Ledbetter, David H.; Levy, Elaine; Craig, Ian W.; Willard, Huntington F. (1991). "Localization of the X inactivation centre on the human X chromosome in Xq13". Nature. 349 (6304): 82–84. Bibcode:1991Natur.349...82B. doi:10.1038/349082a0. PMID 1985270. S2CID 4360783.
Dawson, A. J.; Wickstrom, D. E.; Riordan, D.; Cardwell, S.; Casey, R.; Baldry, S.; Brown, C. (2004). "A unique patient with an Ullrich-Turner syndrome variant and mosaicism for a tiny r(X) and a partial proximal duplication 1q". American Journal of Medical Genetics. Part A. 124A (3): 303–6. doi:10.1002/ajmg.a.20302. PMID 14708105. S2CID 13408738.
Johnson, N. A.; Al-Tourah, A.; Brown, C. J.; Connors, J. M.; Gascoyne, R. D.; Horsman, D. E. (2008). "Prognostic significance of secondary cytogenetic alterations in follicular lymphomas". Genes, Chromosomes & Cancer. 47 (12): 1038–48. doi:10.1002/gcc.20606. PMID 18720523. S2CID 20432234.
Hatakeyama, C.; Anderson, C. L.; Beever, C. L.; Peñaherrera, M. S.; Brown, C. J.; Robinson, W. P. (2004). "The dynamics of X-inactivation skewing as women age". Clinical Genetics. 66 (4): 327–32. doi:10.1111/j.1399-0004.2004.00310.x. PMID 15355435. S2CID 23931974.