| Year |
Citation |
Score |
| 2023 |
Makova KD, Pickett BD, Harris RS, Hartley GA, Cechova M, Pal K, Nurk S, Yoo D, Li Q, Hebbar P, McGrath BC, Antonacci F, Aubel M, Biddanda A, Borchers M, ... ... Carrel L, et al. The Complete Sequence and Comparative Analysis of Ape Sex Chromosomes. Biorxiv : the Preprint Server For Biology. PMID 38077089 DOI: 10.1101/2023.11.30.569198 |
0.684 |
|
| 2021 |
Sauteraud R, Stahl JM, James J, Englebright M, Chen F, Zhan X, Carrel L, Liu DJ. Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases. Genome Research. PMID 34426515 DOI: 10.1101/gr.275677.121 |
0.679 |
|
| 2019 |
Cygan PH, Arnold-Croop SE, Weidman EA, Chen F, Liu DJ, Eyster ME, Carrel L. Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants Blood. 134: 1125-1125. DOI: 10.1182/Blood-2019-126026 |
0.325 |
|
| 2017 |
Carrel L, Brown CJ. When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 372. PMID 28947654 DOI: 10.1098/Rstb.2016.0355 |
0.79 |
|
| 2016 |
Cygan P, Carrel L, Eyster ME. Moderate X-chromosome inactivation skewing underlies factor VIII activity in symptomatic carriers from a family with mild haemophilia A. Haemophilia. 22. PMID 27704658 DOI: 10.1111/Hae.13083 |
0.622 |
|
| 2015 |
Simmons T, Cygan PH, Carrel L, Eyster ME. Role of Von Willebrand Factor in Female Carriers from an Extended Family with Mild Hemophilia A Blood. 126: 3537-3537. DOI: 10.1182/Blood.V126.23.3537.3537 |
0.471 |
|
| 2015 |
Cygan PH, Carrel L, Eyster ME. Correlation of X Chromosome Inactivation Skewing and Bleeding Phenotype in Obligate Carriers of Hemophilia A Blood. 126: 2285-2285. DOI: 10.1182/Blood.V126.23.2285.2285 |
0.493 |
|
| 2013 |
Horvath LM, Li N, Carrel L. Deletion of an X-Inactivation Boundary Disrupts Adjacent Gene Silencing Plos Genetics. 9. PMID 24278033 DOI: 10.1371/Journal.Pgen.1003952 |
0.659 |
|
| 2012 |
Cheung AY, Horvath LM, Carrel L, Ellis J. X-chromosome inactivation in rett syndrome human induced pluripotent stem cells. Frontiers in Psychiatry. 3: 24. PMID 22470355 DOI: 10.3389/Fpsyt.2012.00024 |
0.59 |
|
| 2011 |
Lopes AM, Arnold-Croop SE, Amorim A, Carrel L. Clustered transcripts that escape X inactivation at mouse XqD. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 572-82. PMID 21769671 DOI: 10.1007/S00335-011-9350-6 |
0.749 |
|
| 2011 |
Berletch JB, Yang F, Xu J, Carrel L, Disteche CM. Genes that escape from X inactivation. Human Genetics. 130: 237-45. PMID 21614513 DOI: 10.1007/S00439-011-1011-Z |
0.755 |
|
| 2011 |
Cheung AY, Horvath LM, Grafodatskaya D, Pasceri P, Weksberg R, Hotta A, Carrel L, Ellis J. Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation. Human Molecular Genetics. 20: 2103-15. PMID 21372149 DOI: 10.1093/Hmg/Ddr093 |
0.481 |
|
| 2010 |
Park C, Carrel L, Makova KD. Strong purifying selection at genes escaping X chromosome inactivation. Molecular Biology and Evolution. 27: 2446-50. PMID 20534706 DOI: 10.1093/Molbev/Msq143 |
0.761 |
|
| 2009 |
Prothero KE, Stahl JM, Carrel L. Dosage compensation and gene expression on the mammalian X chromosome: one plus one does not always equal two. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 17: 637-48. PMID 19802704 DOI: 10.1007/S10577-009-9063-9 |
0.432 |
|
| 2009 |
Heard E, Carrel L. Foreword: Coping with sex chromosome imbalance. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 17: 579-83. PMID 19760092 DOI: 10.1007/S10577-009-9062-X |
0.679 |
|
| 2008 |
Li N, Carrel L. Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus. Proceedings of the National Academy of Sciences of the United States of America. 105: 17055-60. PMID 18971342 DOI: 10.1073/Pnas.0807765105 |
0.781 |
|
| 2006 |
Carrel L, Park C, Tyekucheva S, Dunn J, Chiaromonte F, Makova KD. Genomic environment predicts expression patterns on the human inactive X chromosome. Plos Genetics. 2: e151. PMID 17009873 DOI: 10.1371/Journal.Pgen.0020151 |
0.67 |
|
| 2006 |
Carrel L. Molecular biology. "X"-rated chromosomal rendezvous. Science (New York, N.Y.). 311: 1107-9. PMID 16497921 DOI: 10.1126/Science.1124662 |
0.683 |
|
| 2005 |
Carrel L, Willard HF. X-inactivation profile reveals extensive variability in X-linked gene expression in females Nature. 434: 400-404. PMID 15772666 DOI: 10.1038/Nature03479 |
0.841 |
|
| 2005 |
Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, ... ... Carrel L, et al. The DNA sequence of the human X chromosome. Nature. 434: 325-37. PMID 15772651 DOI: 10.1038/Nature03440 |
0.786 |
|
| 2004 |
Carrel L. Evolutionary biology: chromosome chain makes a link. Nature. 432: 817-8. PMID 15602542 DOI: 10.1038/432817A |
0.686 |
|
| 2002 |
Hidaka K, Caffrey JJ, Hua L, Zhang T, Falck JR, Nickel GC, Carrel L, Barnes LD, Shears SB. An adjacent pair of human NUDT genes on chromosome X are preferentially expressed in testis and encode two new isoforms of diphosphoinositol polyphosphate phosphohydrolase. The Journal of Biological Chemistry. 277: 32730-8. PMID 12105228 DOI: 10.1074/Jbc.M205476200 |
0.615 |
|
| 2002 |
Hall LL, Byron M, Sakai K, Carrel L, Willard HF, Lawrence JB. An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells Proceedings of the National Academy of Sciences of the United States of America. 99: 8677-8682. PMID 12072569 DOI: 10.1073/Pnas.132468999 |
0.592 |
|
| 2001 |
Willard HF, Carrel L. Making sense (and antisense) of the X inactivation center Proceedings of the National Academy of Sciences of the United States of America. 98: 10025-10027. PMID 11526224 DOI: 10.1073/Pnas.191380198 |
0.745 |
|
| 2001 |
Tiller GE, Hannig VL, Dozier D, Carrel L, Trevarthen KC, Wilcox WR, Mundlos S, Haines JL, Gedeon AK, Gecz J. A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda. American Journal of Human Genetics. 68: 1398-407. PMID 11326333 DOI: 10.1086/320594 |
0.595 |
|
| 2000 |
Wolff DJ, Schwartz S, Carrel L. Molecular determination of X inactivation pattern correlates with phenotype in women with a structurally abnormal X chromosome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 2: 136-41. PMID 11397327 DOI: 10.1097/00125817-200003000-00004 |
0.688 |
|
| 2000 |
Bailey JA, Carrel L, Chakravarti A, Eichler EE. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis. Proceedings of the National Academy of Sciences of the United States of America. 97: 6634-9. PMID 10841562 DOI: 10.1073/Pnas.97.12.6634 |
0.746 |
|
| 1999 |
Carrel L, Cottle AA, Goglin KC, Willard HF. A first-generation X-inactivation profile of the human X chromosome Proceedings of the National Academy of Sciences of the United States of America. 96: 14440-14444. PMID 10588724 DOI: 10.1073/Pnas.96.25.14440 |
0.77 |
|
| 1999 |
Carrel L, Willard HF. Heterogeneous gene expression from the inactive X chromosome: An X- linked gene that escapes X inactivation in some human cell lines but is inactivated in others Proceedings of the National Academy of Sciences of the United States of America. 96: 7364-7369. PMID 10377420 DOI: 10.1073/Pnas.96.13.7364 |
0.748 |
|
| 1999 |
Mroz K, Carrel L, Hunt PA. Germ cell development in the XXY mouse: evidence that X chromosome reactivation is independent of sexual differentiation. Developmental Biology. 207: 229-38. PMID 10049577 DOI: 10.1006/Dbio.1998.9160 |
0.659 |
|
| 1998 |
Greenfield A, Carrel L, Pennisi D, Philippe C, Quaderi N, Siggers P, Steiner K, Tam PP, Monaco AP, Willard HF, Koopman P. The UTX gene escapes X inactivation in mice and humans. Human Molecular Genetics. 7: 737-42. PMID 9499428 DOI: 10.1093/Hmg/7.4.737 |
0.787 |
|
| 1998 |
Dal Zotto L, Quaderi NA, Elliott R, Lingerfelter PA, Carrel L, Valsecchi V, Montini E, Yen CH, Chapman V, Kalcheva I, Arrigo G, Zuffardi O, Thomas S, Willard HF, Ballabio A, et al. The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Human Molecular Genetics. 7: 489-99. PMID 9467009 DOI: 10.1093/Hmg/7.3.489 |
0.652 |
|
| 1997 |
Brown CJ, Carrel L, Willard HF. Expression of genes from the human active and inactive X chromosomes American Journal of Human Genetics. 60: 1333-1343. PMID 9199554 DOI: 10.1086/515488 |
0.79 |
|
| 1996 |
Carrel L, Hunt PA, Willard HF. Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene Human Molecular Genetics. 5: 1361-1366. PMID 8872478 DOI: 10.1093/Hmg/5.9.1361 |
0.719 |
|
| 1996 |
Carrel L, Clemson CM, Dunn JM, Miller AP, Hunt PA, Lawrence JB, Willard HF. X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Human Molecular Genetics. 5: 391-401. PMID 8852665 DOI: 10.1093/Hmg/5.3.391 |
0.803 |
|
| 1996 |
Carrel L, Willard HF. An assay for X inactivation based on differential methylation at the fragile X locus, FMR1 American Journal of Medical Genetics. 64: 27-30. PMID 8826444 DOI: 10.1002/(Sici)1096-8628(19960712)64:1<27::Aid-Ajmg3>3.0.Co;2-O |
0.744 |
|
| 1996 |
Coleman MP, Ambrose HJ, Carrel L, Németh AH, Willard HF, Davies KE. A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. Genomics. 31: 135-8. PMID 8808293 DOI: 10.1006/Geno.1996.0022 |
0.692 |
|
| 1995 |
Sultana R, Adler DA, Edelhoff S, Carrel L, Lee KH, Chapman VC, Willard HF, Disteche CM. The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. Human Molecular Genetics. 4: 257-63. PMID 7757076 DOI: 10.1093/Hmg/4.2.257 |
0.746 |
|
| 1995 |
Brown CJ, Miller AP, Carrel L, Rupert JL, Davies KE, Willard HF. The DXS423E gene in Xp11.21 escapes X chromosome inactivation. Human Molecular Genetics. 4: 251-5. PMID 7757075 DOI: 10.1093/Hmg/4.2.251 |
0.813 |
|
| 1994 |
Lafrenière RG, Carrel L, Willard HF. A novel transmembrane transporter encoded by the XPCT gene in xq13.2 Human Molecular Genetics. 3: 1133-1139. PMID 7981683 DOI: 10.1093/Hmg/3.7.1133 |
0.761 |
|
| 1993 |
Greig GM, Sharp CB, Carrel L, Willard HF. Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies. Human Molecular Genetics. 2: 1611-8. PMID 8268913 DOI: 10.1093/Hmg/2.10.1611 |
0.684 |
|
| 1993 |
Willard HF, Brown CJ, Carrel L, Hendrich B, Miller AP. Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. Cold Spring Harbor Symposia On Quantitative Biology. 58: 315-22. PMID 7956044 DOI: 10.1101/Sqb.1993.058.01.037 |
0.74 |
|
| 1991 |
Lafrenière RG, Brown CJ, Powers VE, Carrel L, Davies KE, Barker DF, Willard HF. Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. Genomics. 11: 352-63. PMID 1685139 DOI: 10.1016/0888-7543(91)90143-3 |
0.621 |
|
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