| Year |
Citation |
Score |
| 2007 |
Mohrenweiser H. Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes. Mutation Research. 616: 221-6. PMID 17161851 DOI: 10.1016/j.mrfmmm.2006.11.008 |
0.356 |
|
| 2007 |
Jones IM, Thomas CB, Xi T, Mohrenweiser HW, Nelson DO. Exploration of methods to identify polymorphisms associated with variation in DNA repair capacity phenotypes. Mutation Research. 616: 213-20. PMID 17145065 DOI: 10.1016/j.mrfmmm.2006.11.005 |
0.364 |
|
| 2006 |
Hinz JM, Nham PB, Yamada NA, Tebbs RS, Salazar EP, Hinz AK, Mohrenweiser HW, Jones IM, Thompson LH. Four human FANCG polymorphic variants show normal biological function in hamster CHO cells. Mutation Research. 602: 34-42. PMID 17010390 DOI: 10.1016/j.mrfmmm.2006.07.008 |
0.313 |
|
| 2003 |
Blackshear PJ, Phillips RS, Vazquez-Matias J, Mohrenweiser H. Polymorphisms in the genes encoding members of the tristetraprolin family of human tandem CCCH zinc finger proteins. Progress in Nucleic Acid Research and Molecular Biology. 75: 43-68. PMID 14604009 DOI: 10.1016/S0079-6603(03)75002-8 |
0.434 |
|
| 2002 |
Mohrenweiser HW, Xi T, Vázquez-Matías J, Jones IM. Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 11: 1054-64. PMID 12376507 |
0.304 |
|
| 2002 |
King LM, Ma J, Srettabunjong S, Graves J, Bradbury JA, Li L, Spiecker M, Liao JK, Mohrenweiser H, Zeldin DC. Cloning of CYP2J2 gene and identification of functional polymorphisms. Molecular Pharmacology. 61: 840-52. PMID 11901223 DOI: 10.1124/Mol.61.4.840 |
0.408 |
|
| 2002 |
Qiao Y, Spitz MR, Shen H, Guo Z, Shete S, Hedayati M, Grossman L, Mohrenweiser H, Wei Q. Modulation of repair of ultraviolet damage in the host-cell reactivation assay by polymorphic XPC and XPD/ERCC2 genotypes. Carcinogenesis. 23: 295-9. PMID 11872635 DOI: 10.1093/Carcin/23.2.295 |
0.346 |
|
| 2000 |
Smith JS, Tachibana I, Lee HK, Qian J, Pohl U, Mohrenweiser HW, Borell TJ, Hosek SM, Soderberg CL, von Deimling A, Perry A, Scheithauer BW, Louis DN, Jenkins RB. Mapping of the chromosome 19 q-arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers. Genes, Chromosomes & Cancer. 29: 16-25. PMID 10918389 DOI: 10.1002/1098-2264(2000)9999:9999<::Aid-Gcc1007>3.3.Co;2-9 |
0.35 |
|
| 2000 |
Coleman MA, Eisen JA, Mohrenweiser HW. Cloning and characterization of HARP/SMARCAL1: a prokaryotic HepA-related SNF2 helicase protein from human and mouse. Genomics. 65: 274-82. PMID 10857751 DOI: 10.1006/Geno.2000.6174 |
0.408 |
|
| 2000 |
Smith JS, Tachibana I, Pohl U, Lee HK, Thanarajasingam U, Portier BP, Ueki K, Ramaswamy S, Billings SJ, Mohrenweiser HW, Louis DN, Jenkins RB. A transcript map of the chromosome 19q-arm glioma tumor suppressor region. Genomics. 64: 44-50. PMID 10708517 DOI: 10.1006/Geno.1999.6101 |
0.343 |
|
| 2000 |
Pohl U, Smith JS, Tachibana I, Ueki K, Lee HK, Ramaswamy S, Wu Q, Mohrenweiser HW, Jenkins RB, Louis DN. EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins. Genomics. 63: 255-62. PMID 10673336 DOI: 10.1006/Geno.1999.6087 |
0.381 |
|
| 1998 |
Her C, Wood TC, Eichler EE, Mohrenweiser HW, Ramagli LS, Siciliano MJ, Weinshilboum RM. Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene. Genomics. 53: 284-95. PMID 9799594 DOI: 10.1006/geno.1998.5518 |
0.514 |
|
| 1998 |
Eichler EE, Hoffman SM, Adamson AA, Gordon LA, McCready P, Lamerdin JE, Mohrenweiser HW. Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12. Genome Research. 8: 791-808. PMID 9724325 |
0.481 |
|
| 1998 |
Ghanshani S, Coleman M, Gustavsson P, Wu AC, Gargus JJ, Gutman GA, Dahl N, Mohrenweiser H, Chandy KG. Human calcium-activated potassium channel gene KCNN4 maps to chromosome 19q13.2 in the region deleted in diamond-blackfan anemia. Genomics. 51: 160-1. PMID 9693050 DOI: 10.1006/Geno.1998.5333 |
0.4 |
|
| 1998 |
Kalman K, Nguyen A, Tseng-Crank J, Dukes ID, Chandy G, Hustad CM, Copeland NG, Jenkins NA, Mohrenweiser H, Brandriff B, Cahalan M, Gutman GA, Chandy KG. Genomic organization, chromosomal localization, tissue distribution, and biophysical characterization of a novel mammalian Shaker-related voltage-gated potassium channel, Kv1.7. The Journal of Biological Chemistry. 273: 5851-7. PMID 9488722 DOI: 10.1074/Jbc.273.10.5851 |
0.321 |
|
| 1998 |
Mohrenweiser HW, Tsujimoto S, Gordon L, Olsen AS. Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19. Genomics. 47: 153-62. PMID 9479487 DOI: 10.1006/geno.1997.5097 |
0.31 |
|
| 1998 |
Shen MR, Zdzienicka MZ, Mohrenweiser H, Thompson LH, Thelen MP. Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair. Nucleic Acids Research. 26: 1032-7. PMID 9461464 DOI: 10.1093/Nar/26.4.1032 |
0.381 |
|
| 1997 |
Ueki K, Ramaswamy S, Billings SJ, Mohrenweiser HW, Louis DN. ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3. Neurogenetics. 1: 31-6. PMID 10735272 DOI: 10.1007/S100480050005 |
0.331 |
|
| 1997 |
Ueki K, Ramaswamy S, Billings SJ, Mohrenweiser HW, Louis DN. Chromosomal localization to 19q13.3, partial genomic structure and 5' cDNA sequence of the human symplekin gene. Somatic Cell and Molecular Genetics. 23: 229-31. PMID 9330635 DOI: 10.1007/Bf02721375 |
0.426 |
|
| 1997 |
Wagtmann N, Rojo S, Eichler E, Mohrenweiser H, Long EO. A new human gene complex encoding the killer cell inhibitory receptors and related monocyte/macrophage receptors. Current Biology : Cb. 7: 615-8. PMID 9259559 DOI: 10.1016/S0960-9822(06)00263-6 |
0.431 |
|
| 1997 |
Eichler EE, Budarf ML, Rocchi M, Deaven LL, Doggett NA, Baldini A, Nelson DL, Mohrenweiser HW. Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Human Molecular Genetics. 6: 991-1002. PMID 9215666 DOI: 10.1093/hmg/6.7.991 |
0.531 |
|
| 1997 |
Nystuen A, Costeff H, Elpeleg ON, Apter N, Bonné-Tamir B, Mohrenweiser H, Haider N, Stone EM, Sheffield VC. Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene. Human Molecular Genetics. 6: 563-9. PMID 9097959 DOI: 10.1093/Hmg/6.4.563 |
0.421 |
|
| 1996 |
Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Mohrenweiser H, Litt M, Hofker MH, Haan J, Ferrari MD, Frants RR. A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group. European Journal of Human Genetics : Ejhg. 4: 321-8. PMID 9043864 DOI: 10.1159/000472226 |
0.501 |
|
| 1996 |
Rosenberg JE, Lisle DK, Burwick JA, Ueki K, von Deimling A, Mohrenweiser HW, Louis DN. Refined deletion mapping of the chromosome 19q glioma tumor suppressor gene to the D19S412-STD interval. Oncogene. 13: 2483-5. PMID 8957092 |
0.344 |
|
| 1996 |
Mohrenweiser H, Olsen A, Archibald A, Beattie C, Burmeister M, Lamerdin J, Lennon G, Stewart E, Stubbs L, Weber JL, Johnson K. Report an abstracts of the third international workshop on human chromosome 19 mapping 1996. Cytogenetics and Cell Genetics. 74: 161-86. PMID 8941368 DOI: 10.1159/000134408 |
0.37 |
|
| 1996 |
Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell. 87: 543-52. PMID 8898206 DOI: 10.1016/S0092-8674(00)81373-2 |
0.31 |
|
| 1996 |
Stubbs L, Carver EA, Shannon ME, Kim J, Geisler J, Generoso EE, Stanford BG, Dunn WC, Mohrenweiser H, Zimmermann W, Watt SM, Ashworth LK. Detailed comparative map of human chromosome 19q and related regions of the mouse genome. Genomics. 35: 499-508. PMID 8812484 DOI: 10.1006/Geno.1996.0390 |
0.483 |
|
| 1996 |
Chou D, Miyashita T, Mohrenweiser HW, Ueki K, Kastury K, Druck T, von Deimling A, Huebner K, Reed JC, Louis DN. The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomas. Cancer Genetics and Cytogenetics. 88: 136-40. PMID 8640722 DOI: 10.1016/0165-4608(95)00341-X |
0.403 |
|
| 1996 |
Hoffman SM, Hromas R, Amemiya C, Mohrenweiser HW. The location of MZF-1 at the telomere of human chromosome 19q makes it vulnerable to degeneration in aging cells. Leukemia Research. 20: 281-3. PMID 8637224 DOI: 10.1016/0145-2126(95)00158-1 |
0.316 |
|
| 1996 |
Ducros A, Nagy T, Alamowitch S, Nibbio A, Joutel A, Vahedi K, Chabriat H, Iba-Zizen MT, Julien J, Davous P, Goas JY, Lyon-Caen O, Dubois B, Ducrocq X, Salsa F, ... ... Mohrenweiser H, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval American Journal of Human Genetics. 58: 171-181. PMID 8554054 |
0.33 |
|
| 1995 |
Yong WH, Ueki K, Chou D, Reeves SA, von Deimling A, Gusella JF, Mohrenweiser HW, Buckler AJ, Louis DN. Cloning of a highly conserved human protein serine-threonine phosphatase gene from the glioma candidate region on chromosome 19q13.3. Genomics. 29: 533-6. PMID 8666404 DOI: 10.1006/Geno.1995.9972 |
0.405 |
|
| 1995 |
Hoffman SM, Fernandez-Salguero P, Gonzalez FJ, Mohrenweiser HW. Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19. Journal of Molecular Evolution. 41: 894-900. PMID 8587134 DOI: 10.1007/BF00173169 |
0.369 |
|
| 1995 |
Gordon LA, Bergmann A, Christensen M, Danganan L, Lee DA, Ashworth LK, Nelson DO, Olsen AS, Mohrenweiser HW, Carrano AV. A 30-Mb metric fluorescence in situ hybridization map of human chromosome 19q. Genomics. 30: 187-94. PMID 8586418 DOI: 10.1006/geno.1995.9886 |
0.301 |
|
| 1995 |
Mohrenweiser H, Zingg B. Mosaicism: the embryo as a target for induction of mutations leading to cancer and genetic disease. Environmental and Molecular Mutagenesis. 25: 21-9. PMID 7789359 DOI: 10.1002/Em.2850250606 |
0.313 |
|
| 1995 |
Otterness DM, Mohrenweiser HW, Brandriff BF, Weinshilboum RM. Dehydroepiandrosterone sulfotransferase gene (STD): localization to human chromosome band 19q13.3. Cytogenetics and Cell Genetics. 70: 45-7. PMID 7736787 |
0.36 |
|
| 1995 |
Levitt RC, Liu Z, Nouri N, Meyers DA, Brandriff B, Mohrenweiser HM. Mapping of the gene for hormone sensitive lipase (LIPE) to chromosome 19q13.1-->q13.2. Cytogenetics and Cell Genetics. 69: 211-4. PMID 7698015 |
0.374 |
|
| 1995 |
Briggs MD, Hoffman SM, King LM, Olsen AS, Mohrenweiser H, Leroy JG, Mortier GR, Rimoin DL, Lachman RS, Gaines ES. Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nature Genetics. 10: 330-6. PMID 7670472 DOI: 10.1038/ng0795-330 |
0.328 |
|
| 1995 |
Fernandez-Salguero P, Hoffman SM, Cholerton S, Mohrenweiser H, Raunio H, Rautio A, Pelkonen O, Huang JD, Evans WE, Idle JR. A genetic polymorphism in coumarin 7-hydroxylation: sequence of the human CYP2A genes and identification of variant CYP2A6 alleles. American Journal of Human Genetics. 57: 651-60. PMID 7668294 |
0.394 |
|
| 1995 |
Yong WH, Chou D, Ueki K, Harsh GR, von Deimling A, Gusella JF, Mohrenweiser HW, Louis DN. Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112. Journal of Neuropathology and Experimental Neurology. 54: 622-6. PMID 7666049 DOI: 10.1097/00005072-199509000-00002 |
0.361 |
|
| 1995 |
Mohrenweiser HW, Tsujimoto S, Tynan K, Lamerdin J, Carrano AV. Unique sequence STSs for 21 cytogenetically mapped loci on human chromosome 19. Cytogenetics and Cell Genetics. 71: 58-61. PMID 7606929 DOI: 10.1159/000134063 |
0.338 |
|
| 1995 |
Ashworth LK, Batzer MA, Brandriff B, Branscomb E, de Jong P, Garcia E, Garnes JA, Gordon LA, Lamerdin JE, Lennon G, Mohrenweiser H, Olsen AS, Slezak T, Carrano AV. An integrated metric physical map of human chromosome 19. Nature Genetics. 11: 422-7. PMID 7493023 DOI: 10.1038/Ng1295-422 |
0.421 |
|
| 1995 |
Laurell H, Grober J, Holst LS, Holm C, Mohrenweiser HW, Langin D. The hormone-sensitive lipase (LIPE) gene located on chromosome 19q13.1-->13.2 is not duplicated on 19p13.3. International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association For the Study of Obesity. 19: 590-2. PMID 7489032 |
0.372 |
|
| 1994 |
Rubio MP, Correa KM, Ueki K, Mohrenweiser HW, Gusella JF, von Deimling A, Louis DN. The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC. Cancer Research. 54: 4760-3. PMID 8062276 |
0.36 |
|
| 1994 |
Brandriff BF, Gordon LA, Fertitta A, Olsen AS, Christensen M, Ashworth LK, Nelson DO, Carrano AV, Mohrenweiser HW. Human chromosome 19p: a fluorescence in situ hybridization map with genomic distance estimates for 79 intervals spanning 20 Mb. Genomics. 23: 582-91. PMID 7851886 DOI: 10.1006/geno.1994.1546 |
0.331 |
|
| 1994 |
Mohrenweiser H. International Commission for Protection Against Environmental Mutagens and Carcinogens. Working paper no. 5. Impact of the molecular spectrum of mutational lesions on estimates of germinal gene-mutation rates. Mutation Research. 304: 119-37. PMID 7506352 DOI: 10.1016/0027-5107(94)90322-0 |
0.431 |
|
| 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 |
0.339 |
|
| 1993 |
Tynan K, Hoffman SM, Tsujimoto S, Brandriff B, Gordon L, Carrano AV, Mohrenweiser HW. Organization of the multiple polymorphic sites of the D19S11 locus within a 650-kb cosmid contig. Genomics. 17: 316-23. PMID 8406482 DOI: 10.1006/geno.1993.1327 |
0.349 |
|
| 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 |
0.311 |
|
| 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 |
0.357 |
|
| 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 |
0.402 |
|
| 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 |
0.348 |
|
| 1992 |
Thompson J, Zimmermann W, Osthus-Bugat P, Schleussner C, Eades-Perner AM, Barnert S, Von Kleist S, Willcocks T, Craig I, Tynan K, Olsen A, Mohrenweiser H. Long-range chromosomal mapping of the carcinoembryonic antigen (CEA) gene family cluster Genomics. 12: 761-772. PMID 1572649 DOI: 10.1016/0888-7543(92)90307-E |
0.407 |
|
| 1992 |
Noguiez P, Barnes DE, Mohrenweiser HW, Lindahl T. Structure of the human DNA ligase I gene. Nucleic Acids Research. 20: 3845-50. PMID 1508669 DOI: 10.1093/nar/20.15.3845 |
0.344 |
|
| 1990 |
Spritz RA, Strunk K, Surowy CS, Mohrenweiser HW. Human U1-70K ribonucleoprotein antigen gene: organization, nucleotide sequence, and mapping to locus 19q13.3. Genomics. 8: 371-9. PMID 2147422 DOI: 10.1016/0888-7543(90)90295-6 |
0.313 |
|
| 1989 |
Mohrenweiser HW, Carrano AV, Fertitta A, Perry B, Thompson LH, Tucker JD, Weber CA. Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19. Cytogenetics and Cell Genetics. 52: 11-4. PMID 2558854 DOI: 10.1159/000132829 |
0.353 |
|
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