| Year |
Citation |
Score |
| 2023 |
Heilig R, Eckenberg R, Petit JL, Fonknechten N, Da Silva C, Cattolico L, Levy M, Barbe V, de Berardinis V, Ureta-Vidal A, Pelletier E, Vico V, Anthouard V, Rowen L, Madan A, ... ... Trask B, et al. Publisher Correction: The DNA sequence and analysis of human chromosome 14. Nature. PMID 37491470 DOI: 10.1038/s41586-023-06403-y |
0.381 |
|
| 2010 |
Hughes JF, Skaletsky H, Pyntikova T, Graves TA, van Daalen SK, Minx PJ, Fulton RS, McGrath SD, Locke DP, Friedman C, Trask BJ, Mardis ER, Warren WC, Repping S, Rozen S, et al. Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content. Nature. 463: 536-9. PMID 20072128 DOI: 10.1038/Nature08700 |
0.432 |
|
| 2009 |
Rudd MK, Endicott RM, Friedman C, Walker M, Young JM, Osoegawa K, de Jong PJ, Green ED, Trask BJ. Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event. Genome Research. 19: 33-41. PMID 18952852 DOI: 10.1101/gr.083170.108 |
0.441 |
|
| 2008 |
Young JM, Endicott RM, Parghi SS, Walker M, Kidd JM, Trask BJ. Extensive copy-number variation of the human olfactory receptor gene family. American Journal of Human Genetics. 83: 228-42. PMID 18674749 DOI: 10.1016/J.Ajhg.2008.07.005 |
0.325 |
|
| 2007 |
Linardopoulou EV, Parghi SS, Friedman C, Osborn GE, Parkhurst SM, Trask BJ. Human subtelomeric WASH genes encode a new subclass of the WASP family. Plos Genetics. 3: e237. PMID 18159949 DOI: 10.1371/Journal.Pgen.0030237 |
0.331 |
|
| 2007 |
Rudd MK, Friedman C, Parghi SS, Linardopoulou EV, Hsu L, Trask BJ. Elevated rates of sister chromatid exchange at chromosome ends. Plos Genetics. 3: e32. PMID 17319749 DOI: 10.1371/journal.pgen.0030032 |
0.302 |
|
| 2005 |
Linardopoulou EV, Williams EM, Fan Y, Friedman C, Young JM, Trask BJ. Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication. Nature. 437: 94-100. PMID 16136133 DOI: 10.1038/nature04029 |
0.417 |
|
| 2005 |
Rowen L, Williams E, Glusman G, Linardopoulou E, Friedman C, Ahearn ME, Seto J, Boysen C, Qin S, Wang K, Kaur A, Bloom S, Hood L, Trask BJ. Interchromosomal segmental duplications explain the unusual structure of PRSS3, the gene for an inhibitor-resistant trypsinogen. Molecular Biology and Evolution. 22: 1712-20. PMID 15901841 DOI: 10.1093/Molbev/Msi166 |
0.358 |
|
| 2004 |
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Månér S, Massa H, Walker M, Chi M, Navin N, Lucito R, Healy J, Hicks J, Ye K, ... ... Trask B, et al. Large-scale copy number polymorphism in the human genome. Science (New York, N.Y.). 305: 525-8. PMID 15273396 DOI: 10.1126/Science.1098918 |
0.373 |
|
| 2004 |
Gibbs RA, Weinstock GM, Metzker ML, Muzny DM, Sodergren EJ, Scherer S, Scott G, Steffen D, Worley KC, Burch PE, Okwuonu G, Hines S, Lewis L, DeRamo C, Delgado O, ... ... Trask BJ, et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 428: 493-521. PMID 15057822 DOI: 10.1038/Nature02426 |
0.335 |
|
| 2003 |
Heilig R, Eckenberg R, Petit JL, Fonknechten N, Da Silva C, Cattolico L, Levy M, Barbe V, de Berardinis V, Ureta-Vidal A, Pelletier E, Vico V, Anthouard V, Rowen L, Madan A, ... ... Trask B, et al. The DNA sequence and analysis of human chromosome 14. Nature. 421: 601-7. PMID 12508121 DOI: 10.1038/nature01348 |
0.46 |
|
| 2002 |
Fan Y, Newman T, Linardopoulou E, Trask BJ. Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions. Genome Research. 12: 1663-72. PMID 12421752 DOI: 10.1101/gr.338402 |
0.377 |
|
| 2002 |
Fan Y, Linardopoulou E, Friedman C, Williams E, Trask BJ. Genomic structure and evolution of the ancestral chromosome fusion site in 2q13-2q14.1 and paralogous regions on other human chromosomes. Genome Research. 12: 1651-62. PMID 12421751 DOI: 10.1101/gr.337602 |
0.444 |
|
| 2002 |
Trask BJ. Human cytogenetics: 46 chromosomes, 46 years and counting. Nature Reviews. Genetics. 3: 769-78. PMID 12360235 DOI: 10.1038/nrg905 |
0.344 |
|
| 2002 |
Sultana R, Yu CE, Yu J, Munson J, Chen D, Hua W, Estes A, Cortes F, de la Barra F, Yu D, Haider ST, Trask BJ, Green ED, Raskind WH, Disteche CM, et al. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics. 80: 129-34. PMID 12160723 DOI: 10.1006/Geno.2002.6810 |
0.321 |
|
| 2002 |
Gygi MP, Ferguson MD, Mefford HC, Lund KP, O'Day C, Zhou P, Friedman C, van den Engh G, Stolowitz ML, Trask BJ. Use of fluorescent sequence-specific polyamides to discriminate human chromosomes by microscopy and flow cytometry. Nucleic Acids Research. 30: 2790-9. PMID 12087162 |
0.443 |
|
| 2002 |
Mefford HC, Trask BJ. The complex structure and dynamic evolution of human subtelomeres. Nature Reviews. Genetics. 3: 91-102. PMID 11836503 DOI: 10.1038/nrg727 |
0.389 |
|
| 2002 |
Lane RP, Roach JC, Lee IY, Boysen C, Smit A, Trask BJ, Hood L. Genomic analysis of the olfactory receptor region of the mouse and human T-cell receptor alpha/delta loci. Genome Research. 12: 81-7. PMID 11779833 DOI: 10.1101/Gr.197901 |
0.322 |
|
| 2001 |
Kouros-Mehr H, Pintchovski S, Melnyk J, Chen YJ, Friedman C, Trask B, Shizuya H. Identification of non-functional human VNO receptor genes provides evidence for vestigiality of the human VNO. Chemical Senses. 26: 1167-74. PMID 11705802 DOI: 10.1093/Chemse/26.9.1167 |
0.451 |
|
| 2001 |
Linardopoulou E, Mefford HC, Nguyen O, Friedman C, van den Engh G, Farwell DG, Coltrera M, Trask BJ. Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location. Human Molecular Genetics. 10: 2373-83. PMID 11689484 |
0.336 |
|
| 2001 |
Mefford HC, Linardopoulou E, Coil D, van den Engh G, Trask BJ. Comparative sequencing of a multicopy subtelomeric region containing olfactory receptor genes reveals multiple interactions between non-homologous chromosomes. Human Molecular Genetics. 10: 2363-72. PMID 11689483 |
0.459 |
|
| 2001 |
Lane RP, Cutforth T, Young J, Athanasiou M, Friedman C, Rowen L, Evans G, Axel R, Hood L, Trask BJ. Genomic analysis of orthologous mouse and human olfactory receptor loci. Proceedings of the National Academy of Sciences of the United States of America. 98: 7390-5. PMID 11416212 DOI: 10.1073/Pnas.131215398 |
0.349 |
|
| 2001 |
Bailey JA, Yavor AM, Massa HF, Trask BJ, Eichler EE. Segmental duplications: organization and impact within the current human genome project assembly. Genome Research. 11: 1005-17. PMID 11381028 DOI: 10.1101/Gr.187101 |
0.372 |
|
| 2001 |
Cheung VG, Nowak N, Jang W, Kirsch IR, Zhao S, Chen XN, Furey TS, Kim UJ, Kuo WL, Olivier M, Conroy J, Kasprzyk A, Massa H, Yonescu R, Sait S, ... ... Trask BJ, et al. Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature. 409: 953-8. PMID 11237021 DOI: 10.1038/35057192 |
0.444 |
|
| 2001 |
McPherson JD, Marra M, Hillier L, Waterston RH, Chinwalla A, Wallis J, Sekhon M, Wylie K, Mardis ER, Wilson RK, Fulton R, Kucaba TA, Wagner-McPherson C, Barbazuk WB, Gregory SG, ... ... Trask B, et al. A physical map of the human genome. Nature. 409: 934-41. PMID 11237014 DOI: 10.1038/35057157 |
0.431 |
|
| 2001 |
Olivier M, Aggarwal A, Allen J, Almendras AA, Bajorek ES, Beasley EM, Brady SD, Bushard JM, Bustos VI, Chu A, Chung TR, De Witte A, Denys ME, Dominguez R, Fang NY, ... ... Trask BJ, et al. A high-resolution radiation hybrid map of the human genome draft sequence. Science (New York, N.Y.). 291: 1298-302. PMID 11181994 DOI: 10.1126/Science.1057437 |
0.324 |
|
| 2000 |
Siegel AF, van den Engh G, Hood L, Trask B, Roach JC. Modeling the feasibility of whole genome shotgun sequencing using a pairwise end strategy. Genomics. 68: 237-46. PMID 10995565 DOI: 10.1006/Geno.2000.6303 |
0.4 |
|
| 2000 |
Singer MJ, Mesner LD, Friedman CL, Trask BJ, Hamlin JL. Amplification of the human dihydrofolate reductase gene via double minutes is initiated by chromosome breaks. Proceedings of the National Academy of Sciences of the United States of America. 97: 7921-6. PMID 10859355 DOI: 10.1073/pnas.130194897 |
0.433 |
|
| 2000 |
Sachs RK, Hlatky LR, Trask BJ. Radiation-produced chromosome aberrations: colourful clues. Trends in Genetics : Tig. 16: 143-6. PMID 10729825 DOI: 10.1016/S0168-9525(99)01960-5 |
0.303 |
|
| 2000 |
Deng Y, Madan A, Banta AB, Friedman C, Trask BJ, Hood L, Li L. Characterization, chromosomal localization, and the complete 30-kb DNA sequence of the human Jagged2 (JAG2) gene. Genomics. 63: 133-8. PMID 10662552 DOI: 10.1006/Geno.1999.6045 |
0.447 |
|
| 1999 |
Vissinga CS, Yeo TC, Woessner J, Massa HF, Wilson RK, Trask BJ, Concannon P. Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome. Cytogenetics and Cell Genetics. 87: 80-4. PMID 10640816 DOI: 10.1159/000015396 |
0.402 |
|
| 1999 |
Roach JC, Siegel AF, van den Engh G, Trask B, Hood L. Gaps in the Human Genome Project. Nature. 401: 843-5. PMID 10553897 DOI: 10.1038/44684 |
0.332 |
|
| 1999 |
DeSilva U, Massa H, Trask BJ, Green ED. Comparative mapping of the region of human chromosome 7 deleted in williams syndrome. Genome Research. 9: 428-36. PMID 10330122 DOI: 10.1101/Gr.9.5.428 |
0.457 |
|
| 1999 |
Siegel AF, Trask B, Roach JC, Mahairas GG, Hood L, van den Engh G. Analysis of sequence-tagged-connector strategies for DNA sequencing. Genome Research. 9: 297-307. PMID 10077536 DOI: 10.1101/Gr.9.3.297 |
0.365 |
|
| 1999 |
Brand-Arpon V, Rouquier S, Massa H, de Jong PJ, Ferraz C, Ioannou PA, Demaille JG, Trask BJ, Giorgi D. A genomic region encompassing a cluster of olfactory receptor genes and a myosin light chain kinase (MYLK) gene is duplicated on human chromosome regions 3q13-q21 and 3p13. Genomics. 56: 98-110. PMID 10036190 DOI: 10.1006/geno.1998.5690 |
0.356 |
|
| 1999 |
Katz SG, Schneider SS, Bartuski A, Trask BJ, Massa H, Overhauser J, Lalande M, Lansdorp PM, Silverman GA. An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA. Human Molecular Genetics. 8: 87-92. PMID 9887335 DOI: 10.1093/Hmg/8.1.87 |
0.402 |
|
| 1998 |
Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes. Human Genetics. 103: 590-9. PMID 9860302 DOI: 10.1007/S004390050874 |
0.336 |
|
| 1998 |
Bartuski AJ, Kamachi Y, Schick C, Massa H, Trask BJ, Silverman GA. A murine ortholog of the human serpin SCCA2 maps to chromosome 1 and inhibits chymotrypsin-like serine proteinases. Genomics. 54: 297-306. PMID 9828132 DOI: 10.1006/geno.1998.5586 |
0.357 |
|
| 1998 |
Trask BJ, Massa H, Brand-Arpon V, Chan K, Friedman C, Nguyen OT, Eichler E, van den Engh G, Rouquier S, Shizuya H, Giorgi D. Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome. Human Molecular Genetics. 7: 2007-20. PMID 9817916 DOI: 10.1093/Hmg/7.13.2007 |
0.459 |
|
| 1998 |
Rouquier S, Friedman C, Delettre C, van den Engh G, Blancher A, Crouau-Roy B, Trask BJ, Giorgi D. A gene recently inactivated in human defines a new olfactory receptor family in mammals. Human Molecular Genetics. 7: 1337-45. PMID 9700185 DOI: 10.1093/hmg/7.9.1337 |
0.381 |
|
| 1998 |
Li L, Huang GM, Banta AB, Deng Y, Smith T, Dong P, Friedman C, Chen L, Trask BJ, Spies T, Rowen L, Hood L. Cloning, characterization, and the complete 56.8-kilobase DNA sequence of the human NOTCH4 gene. Genomics. 51: 45-58. PMID 9693032 DOI: 10.1006/Geno.1998.5330 |
0.301 |
|
| 1998 |
Rouquier S, Taviaux S, Trask BJ, Brand-Arpon V, van den Engh G, Demaille J, Giorgi D. Distribution of olfactory receptor genes in the human genome. Nature Genetics. 18: 243-50. PMID 9500546 DOI: 10.1038/ng0398-243 |
0.446 |
|
| 1998 |
Sharma V, Poorkaj P, Hisama F, Bonnycastle L, Yu CE, Massa H, Trask B, Clancy KP, Patterson D, Weissman SM, Schellenberg GD. An expression map from human chromosome 14q24.3. Genomics. 47: 314-8. PMID 9479506 DOI: 10.1006/Geno.1997.5106 |
0.489 |
|
| 1998 |
Trask BJ, Friedman C, Martin-Gallardo A, Rowen L, Akinbami C, Blankenship J, Collins C, Giorgi D, Iadonato S, Johnson F, Kuo WL, Massa H, Morrish T, Naylor S, Nguyen OT, et al. Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes. Human Molecular Genetics. 7: 13-26. PMID 9384599 DOI: 10.1093/Hmg/7.1.13 |
0.42 |
|
| 1997 |
Mefford H, van den Engh G, Friedman C, Trask BJ. Analysis of the variation in chromosome size among diverse human populations by bivariate flow karyotyping. Human Genetics. 100: 138-44. PMID 9225983 DOI: 10.1007/S004390050479 |
0.345 |
|
| 1997 |
Wise CA, Clines GA, Massa H, Trask BJ, Lovett M. Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family. Genome Research. 7: 10-6. PMID 9037597 DOI: 10.1101/Gr.7.1.10 |
0.407 |
|
| 1997 |
Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, et al. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus. Genomics. 39: 55-65. PMID 9027486 DOI: 10.1006/Geno.1996.4466 |
0.499 |
|
| 1996 |
Trask BJ, Mefford H, van den Engh G, Massa HF, Juyal RC, Potocki L, Finucane B, Abuelo DN, Witt DR, Magenis E, Baldini A, Greenberg F, Lupski JR, Patel PI. Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients. Human Genetics. 98: 710-8. PMID 8931707 DOI: 10.1007/S004390050291 |
0.34 |
|
| 1996 |
Yu CE, Oshima J, Hisama FM, Matthews S, Trask BJ, Schellenberg GD. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21. Genomics. 35: 431-40. PMID 8812476 DOI: 10.1006/Geno.1996.0382 |
0.317 |
|
| 1996 |
Ignatius J, Knuutila S, Scherer SW, Trask B, Kere J. Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3. Journal of Medical Genetics. 33: 507-10. PMID 8782053 DOI: 10.1136/Jmg.33.6.507 |
0.369 |
|
| 1996 |
Liao X, Ma C, Trask B, Massa H, Gilbert DJ, Staudt LM, Jenkins NA, Copeland NG. LAF4 maps to mouse chromosome 1 and human chromosome 2q11.2-q12. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 467-8. PMID 8662235 DOI: 10.1007/S003359900137 |
0.377 |
|
| 1996 |
Gorski JL, Bialecki MD, McDonald MT, Massa HF, Trask BJ, Burright EN. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig. Genomics. 35: 338-45. PMID 8661147 DOI: 10.1006/geno.1996.0365 |
0.359 |
|
| 1995 |
Bryson GL, Massa H, Trask BJ, Van Etten RL. Gene structure, sequence, and chromosomal localization of the human red cell-type low-molecular-weight acid phosphotyrosyl phosphatase gene, ACP1. Genomics. 30: 133-40. PMID 8586411 DOI: 10.1006/geno.1995.9893 |
0.413 |
|
| 1995 |
Juyal RC, Greenberg F, Mengden GA, Lupski JR, Trask BJ, van den Engh G, Lindsay EA, Christy H, Chen KS, Baldini A. Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization. American Journal of Medical Genetics. 58: 286-91. PMID 8533833 DOI: 10.1002/Ajmg.1320580317 |
0.314 |
|
| 1995 |
Yokota H, van den Engh G, Mostert M, Trask BJ. Treatment of cells with alkaline borate buffer extends the capability of interphase FISH mapping. Genomics. 25: 485-91. PMID 7789982 DOI: 10.1016/0888-7543(95)80049-R |
0.377 |
|
| 1995 |
Wilson AC, Parrish JE, Massa HF, Nelson DL, Trask BJ, Herr W. The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney. Genomics. 25: 462-8. PMID 7789979 DOI: 10.1016/0888-7543(95)80046-O |
0.312 |
|
| 1995 |
Silverman GA, Schneider SS, Massa HF, Flint A, Lalande M, Leonard JC, Overhauser J, van den Engh G, Trask BJ. The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2. American Journal of Human Genetics. 56: 926-37. PMID 7717403 |
0.325 |
|
| 1995 |
Sachs RK, van den Engh G, Trask B, Yokota H, Hearst JE. A random-walk/giant-loop model for interphase chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 92: 2710-4. PMID 7708711 DOI: 10.1073/Pnas.92.7.2710 |
0.329 |
|
| 1995 |
Hui SM, Trask B, van den Engh G, Bartuski AJ, Smith A, Flint A, Lalande M, Silverman GA. Analysis of randomly amplified flow-sorted chromosomes using the polymerase chain reaction. Genomics. 26: 364-71. PMID 7601463 DOI: 10.1016/0888-7543(95)80221-7 |
0.381 |
|
| 1995 |
Martin-Gallardo A, Lamerdin J, Sopapan P, Friedman C, Fertitta AL, Garcia E, Carrano A, Negorev D, Macina RA, Trask BJ. Molecular analysis of a novel subtelomeric repeat with polymorphic chromosomal distribution. Cytogenetics and Cell Genetics. 71: 289-95. PMID 7587396 DOI: 10.1159/000134129 |
0.444 |
|
| 1995 |
Yokota H, van den Engh G, Hearst JE, Sachs RK, Trask BJ. Evidence for the organization of chromatin in megabase pair-sized loops arranged along a random walk path in the human G0/G1 interphase nucleus. The Journal of Cell Biology. 130: 1239-49. PMID 7559748 DOI: 10.1083/Jcb.130.6.1239 |
0.419 |
|
| 1995 |
Rouquier S, Trask BJ, Taviaux S, van den Engh G, Diriong S, Lennon GG, Giorgi D. Direct selection of cDNAs using whole chromosomes. Nucleic Acids Research. 23: 4415-20. PMID 7501464 DOI: 10.1093/nar/23.21.4415 |
0.399 |
|
| 1994 |
Green ED, Idol JR, Mohr-Tidwell RM, Braden VV, Peluso DC, Fulton RS, Massa HF, Magness CL, Wilson AM, Kimura J, Weissenbach J, Trask BJ. Integration of physical, genetic and cytogenetic maps of human chromosome 7: Isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers Human Molecular Genetics. 3: 489-501. PMID 8012362 |
0.347 |
|
| 1994 |
Scherer SW, Poorkaj P, Massa H, Soder S, Allen T, Nunes M, Geshuri D, Wong E, Belloni E, Little S, Zhou L, Becker D, Kere J, Ignatius J, Niikawa N, ... ... Trask B, et al. Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly Human Molecular Genetics. 3: 1345-1354. PMID 7987313 DOI: 10.1093/Hmg/3.8.1345 |
0.458 |
|
| 1994 |
Bonnycastle LL, Yu CE, Hunt CR, Trask BJ, Clancy KP, Weber JL, Patterson D, Schellenberg GD. Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2). Genomics. 23: 85-93. PMID 7829106 DOI: 10.1006/Geno.1994.1462 |
0.398 |
|
| 1993 |
Gurrieri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Schindler D, Dietz-Band J, Vergnaud G, Scherer SW. Physical mapping of the holoprosencephaly critical region on chromosome 7q36. Nature Genetics. 3: 247-51. PMID 8485580 DOI: 10.1038/Ng0393-247 |
0.358 |
|
| 1993 |
Ma C, Martin S, Trask B, Hamlin JL. Sister chromatid fusion initiates amplification of the dihydrofolate reductase gene in Chinese hamster cells. Genes & Development. 7: 605-20. PMID 8458577 DOI: 10.1101/gad.7.4.605 |
0.393 |
|
| 1993 |
Trask B, Fertitta A, Christensen M, Youngblom J, Bergmann A, Copeland A, de Jong P, Mohrenweiser H, Olsen A, Carrano A. Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers. Genomics. 15: 133-45. PMID 8432525 DOI: 10.1006/geno.1993.1021 |
0.422 |
|
| 1993 |
Rouquier S, Giorgi D, Trask B, Bergmann A, Phillips MS, MacLennan DH, de Jong P. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene. Genomics. 17: 330-40. PMID 8406483 DOI: 10.1006/Geno.1993.1329 |
0.504 |
|
| 1993 |
Pasteris NG, Trask BJ, Sheldon S, Gorski JL. Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35. Human Molecular Genetics. 2: 953-9. PMID 8103404 |
0.371 |
|
| 1993 |
Trask BJ, Allen S, Massa H, Fertitta A, Sachs R, van den Engh G, Wu M. Studies of metaphase and interphase chromosomes using fluorescence in situ hybridization. Cold Spring Harbor Symposia On Quantitative Biology. 58: 767-75. PMID 7956093 DOI: 10.1101/Sqb.1993.058.01.084 |
0.427 |
|
| 1993 |
Malo D, Gros P, Bergmann A, Trask B, Mohrenweiser HW, Canfield VA, Levenson R. Genes encoding the H,K-ATPase alpha and Na,K-ATPase alpha 3 subunits are linked on mouse chromosome 7 and human chromosome 19. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 644-9. PMID 7904196 DOI: 10.1007/Bf00360901 |
0.33 |
|
| 1993 |
Trask B, Fertitta A, Christensen M, Allen S, Segraves M, Bergmann A, Massa H, Sachs R, Engh Gvd. Fluorescence in situ hybridization to metaphase and interphase chromosomes Cancer Genetics and Cytogenetics. 66: 141. DOI: 10.1016/0165-4608(93)90252-H |
0.407 |
|
| 1992 |
Barnes DE, Kodama K, Tynan K, Trask BJ, Christensen M, De Jong PJ, Spurr NK, Lindahl T, Mohrenweiser HW. Assignment of the gene encoding DNA ligase I to human chromosome 19q13.2-13.3. Genomics. 12: 164-6. PMID 1733856 DOI: 10.1016/0888-7543(92)90422-O |
0.412 |
|
| 1992 |
Guzzetta V, Franco B, Trask BJ, Zhang H, Saucedo-Cardenas O, Montes de Oca-Luna R, Greenberg F, Chinault AC, Lupski JR, Patel PI. Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p. Genomics. 13: 551-9. PMID 1639385 DOI: 10.1016/0888-7543(92)90124-B |
0.445 |
|
| 1992 |
Tynan K, Olsen A, Trask B, de Jong P, Thompson J, Zimmermann W, Carrano A, Mohrenweiser H. Assembly and analysis of cosmid contigs in the CEA-gene family region of human chromosome 19. Nucleic Acids Research. 20: 1629-36. PMID 1579453 DOI: 10.1093/Nar/20.7.1629 |
0.494 |
|
| 1992 |
Brandriff BF, Gordon LA, Tynan KT, Olsen AS, Mohrenweiser HW, Fertitta A, Carrano AV, Trask BJ. Order and genomic distances among members of the carcinoembryonic antigen (CEA) gene family determined by fluorescence in situ hybridization. Genomics. 12: 773-9. PMID 1572650 DOI: 10.1016/0888-7543(92)90308-F |
0.421 |
|
| 1992 |
Samson F, de Jong PJ, Trask BJ, Koza-Taylor P, Speer MC, Potter T, Roses AD, Gilbert JR. Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis. Genomics. 13: 1374-5. PMID 1505979 DOI: 10.1016/0888-7543(92)90077-6 |
0.324 |
|
| 1992 |
McCabe ER, Towbin JA, van den Engh G, Trask BJ. Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints. American Journal of Human Genetics. 51: 1277-85. PMID 1463011 |
0.349 |
|
| 1992 |
Hendricks-Taylor LR, Bachinski LL, Siciliano MJ, Fertitta A, Trask B, de Jong PJ, Ledbetter DH, Darlington GJ. The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1. Genomics. 14: 12-7. PMID 1427819 DOI: 10.1016/S0888-7543(05)80276-9 |
0.405 |
|
| 1992 |
van den Engh G, Sachs R, Trask BJ. Estimating genomic distance from DNA sequence location in cell nuclei by a random walk model. Science (New York, N.Y.). 257: 1410-2. PMID 1388286 DOI: 10.1126/Science.1388286 |
0.427 |
|
| 1992 |
Schmitz A, Guilly MN, Trask B, van den Engh G. Immunofluorescent labeling of centromeres for flow cytometric analysis. Cytometry. 13: 478-84. PMID 1378781 DOI: 10.1002/cyto.990130505 |
0.34 |
|
| 1992 |
Trask B, Christensen M, Fertitta A, Bergmann A, Ashworth L, Branscomb E, Carrano A, Van Den Engh G. Fluorescence in situ hybridization mapping of human chromosome 19: mapping and verification of cosmid contigs formed by random restriction enzyme fingerprinting. Genomics. 14: 162-7. PMID 1330881 DOI: 10.1016/S0888-7543(05)80299-X |
0.37 |
|
| 1992 |
Patel PI, Roa BB, Welcher AA, Schoener-Scott R, Trask BJ, Pentao L, Snipes GJ, Garcia CA, Francke U, Shooter EM, Lupski JR, Suter U. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nature Genetics. 1: 159-65. PMID 1303228 DOI: 10.1038/Ng0692-159 |
0.407 |
|
| 1991 |
Trask BJ, van den Engh G, Christensen M, Massa HF, Gray JW, Van Dilla M. Characterization of somatic cell hybrids by bivariate flow karyotyping and fluorescence in situ hybridization. Somatic Cell and Molecular Genetics. 17: 117-36. PMID 2011792 DOI: 10.1007/BF01232970 |
0.393 |
|
| 1991 |
Trask BJ, Massa H, Kenwrick S, Gitschier J. Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei. American Journal of Human Genetics. 48: 1-15. PMID 1985451 |
0.403 |
|
| 1991 |
Kwiatkowski TJ, Beaudet AL, Trask BJ, Zoghbi HY. Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: analysis of dinucleotide polymorphisms on native gels. Genomics. 10: 921-6. PMID 1916824 DOI: 10.1016/0888-7543(91)90180-M |
0.412 |
|
| 1991 |
Brandriff BF, Gordon LA, Trask BJ. DNA sequence mapping by fluorescence in situ hybridization. Environmental and Molecular Mutagenesis. 18: 259-62. PMID 1748088 DOI: 10.1002/em.2850180410 |
0.321 |
|
| 1991 |
Franco B, Lai LW, Patterson D, Ledbetter DH, Trask BJ, van den Engh G, Iannaccone S, Frances S, Patel PI, Lupski JR. Molecular characterization of a patient with del(1)(q23-q25). Human Genetics. 87: 269-77. PMID 1677922 DOI: 10.1007/Bf00200903 |
0.337 |
|
| 1991 |
Lupski JR, de Oca-Luna RM, Slaugenhaupt S, Pentao L, Guzzetta V, Trask BJ, Saucedo-Cardenas O, Barker DF, Killian JM, Garcia CA, Chakravarti A, Patel PI. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell. 66: 219-32. PMID 1677316 DOI: 10.1016/0092-8674(91)90613-4 |
0.327 |
|
| 1990 |
Gray JW, Kuo WL, Liang J, Pinkel D, van den Engh G, Trask B, Tkachuk D, Waldman F, Westbrook C. Analytical approaches to detection and characterization of disease-linked chromosome aberrations. Bone Marrow Transplantation. 6: 14-9. PMID 2202466 |
0.307 |
|
| 1990 |
Trask B, van den Engh G, Nussbaum R, Schwartz C, Gray J. Quantification of the DNA content of structurally abnormal X chromosomes and X chromosome aneuploidy using high resolution bivariate flow karyotyping. Cytometry. 11: 184-95. PMID 2106419 DOI: 10.1002/Cyto.990110121 |
0.339 |
|
| 1989 |
van Dekken H, Pinkel D, Mullikin J, Trask B, van den Engh G, Gray J. Three-dimensional analysis of the organization of human chromosome domains in human and human-hamster hybrid interphase nuclei. Journal of Cell Science. 94: 299-306. PMID 2621226 |
0.413 |
|
| 1989 |
Trask BJ, Hamlin JL. Early dihydrofolate reductase gene amplification events in CHO cells usually occur on the same chromosome arm as the original locus. Genes & Development. 3: 1913-25. PMID 2620827 |
0.427 |
|
| 1989 |
Trask B, Pinkel D, van den Engh G. The proximity of DNA sequences in interphase cell nuclei is correlated to genomic distance and permits ordering of cosmids spanning 250 kilobase pairs. Genomics. 5: 710-7. PMID 2591960 |
0.344 |
|
| 1989 |
Schnur RE, Trask BJ, van den Engh G, Punnett HH, Kistenmacher M, Tomeo MA, Naids RE, Nussbaum RL. An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry. American Journal of Human Genetics. 45: 706-20. PMID 2573275 |
0.306 |
|
| 1989 |
van Dekken H, Pinkel D, Mullikin J, Trask B, van den Engh G, Gray J. Three dimensional reconstruction of human chromosomes in hybrid and human cell line nuclei using fluorescence in situ hybridization. Acta Histochemica. Supplementband. 37: 91-4. PMID 2505327 |
0.331 |
|
| 1989 |
Merry DE, Lesko JG, Sosnoski DM, Lewis RA, Lubinsky M, Trask B, van den Engh G, Collins FS, Nussbaum RL. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. American Journal of Human Genetics. 45: 530-40. PMID 2491012 |
0.42 |
|
| 1989 |
Trask B, van den Engh G, Mayall B, Gray JW. Chromosome heteromorphism quantified by high-resolution bivariate flow karyotyping. American Journal of Human Genetics. 45: 739-52. PMID 2479266 |
0.377 |
|
| 1988 |
Gray JW, Trask B, van den Engh G, Silva A, Lozes C, Grell S, Schonberg S, Yu LC, Golbus MS. Application of flow karyotyping in prenatal detection of chromosome aberrations. American Journal of Human Genetics. 42: 49-59. PMID 3337112 |
0.327 |
|
| 1988 |
Martin AO, Northrup H, Ledbetter DH, Trask B, van den Engh G, Le Beau MM, Beaudet AL, Gray JW, Sekhon G, Krassikoff N. Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis. American Journal of Medical Genetics. 31: 643-54. PMID 3228143 DOI: 10.1002/Ajmg.1320310320 |
0.3 |
|
| 1988 |
Trask B, van den Engh G, Pinkel D, Mullikin J, Waldman F, van Dekken H, Gray J. Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization. Human Genetics. 78: 251-9. PMID 3162226 DOI: 10.1007/BF00291672 |
0.36 |
|
| 1987 |
Patterson M, Schwartz C, Bell M, Sauer S, Hofker M, Trask B, van den Engh G, Davies KE. Physical mapping studies on the human X chromosome in the region Xq27-Xqter. Genomics. 1: 297-306. PMID 3482420 DOI: 10.1016/0888-7543(87)90028-0 |
0.335 |
|
| 1987 |
Gray JW, Dean PN, Fuscoe JC, Peters DC, Trask BJ, van den Engh GJ, Van Dilla MA. High-speed chromosome sorting. Science (New York, N.Y.). 238: 323-9. PMID 2443974 DOI: 10.1126/SCIENCE.2443974 |
0.39 |
|
| 1986 |
Gray JW, Lucas J, Peters D, Pinkel D, Trask B, van den Engh G, Van Dilla M. Flow karyotyping and sorting of human chromosomes. Cold Spring Harbor Symposia On Quantitative Biology. 51: 141-9. PMID 3472710 DOI: 10.1101/SQB.1986.051.01.017 |
0.323 |
|
| 1986 |
van den Engh GJ, Trask BJ, Gray JW. The binding kinetics and interaction of DNA fluorochromes used in the analysis of nuclei and chromosomes by flow cytometry. Histochemistry. 84: 501-8. PMID 2424868 DOI: 10.1007/BF00482983 |
0.301 |
|
| 1985 |
van den Engh GJ, Trask BJ, Gray JW, Langlois RG, Yu LC. Preparation and bivariate analysis of suspensions of human chromosomes. Cytometry. 6: 92-100. PMID 2579781 DOI: 10.1002/cyto.990060203 |
0.354 |
|
| 1984 |
Trask B, van den Engh G, Gray J, Vanderlaan M, Turner B. Immunofluorescent detection of histone 2B on metaphase chromosomes using flow cytometry. Chromosoma. 90: 295-302. PMID 6391869 DOI: 10.1007/BF00287038 |
0.322 |
|
| 1984 |
van den Engh G, Trask B, Cram S, Bartholdi M. Preparation of chromosome suspensions for flow cytometry. Cytometry. 5: 108-17. PMID 6201326 DOI: 10.1002/cyto.990050203 |
0.339 |
|
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