| Year |
Citation |
Score |
| 2021 |
Hassold TJ, Hunt PA. Missed connections: Recombination and human aneuploidy. Prenatal Diagnosis. PMID 33484483 DOI: 10.1002/pd.5910 |
0.588 |
|
| 2020 |
Hassold T, Maylor-Hagen H, Wood A, Gruhn J, Hoffmann E, Broman KW, Hunt P. Failure to recombine is a common feature of human oogenesis. American Journal of Human Genetics. PMID 33306948 DOI: 10.1016/j.ajhg.2020.11.010 |
0.813 |
|
| 2019 |
Chernus JM, Allen EG, Zeng Z, Hoffman ER, Hassold TJ, Feingold E, Sherman SL. A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Plos Genetics. 15: e1008414. PMID 31830031 DOI: 10.1371/Journal.Pgen.1008414 |
0.311 |
|
| 2017 |
Horan TS, Marre A, Hassold T, Lawson C, Hunt PA. Correction: Germline and reproductive tract effects intensify in male mice with successive generations of estrogenic exposure. Plos Genetics. 13: e1006980. PMID 28854188 DOI: 10.1371/journal.pgen.1006980 |
0.751 |
|
| 2017 |
Horan TS, Marre A, Hassold T, Lawson C, Hunt PA. Germline and reproductive tract effects intensify in male mice with successive generations of estrogenic exposure. Plos Genetics. 13: e1006885. PMID 28727826 DOI: 10.1371/Journal.Pgen.1006885 |
0.759 |
|
| 2017 |
Wang S, Hassold T, Hunt P, White MA, Zickler D, Kleckner N, Zhang L. Inefficient Crossover Maturation Underlies Elevated Aneuploidy in Human Female Meiosis. Cell. PMID 28262352 DOI: 10.1016/J.Cell.2017.02.002 |
0.671 |
|
| 2016 |
Hardy K, Hardy PJ, Jacobs PA, Lewallen K, Hassold TJ. Temporal changes in chromosome abnormalities in human spontaneous abortions: Results of 40 years of analysis. American Journal of Medical Genetics. Part A. PMID 27287007 DOI: 10.1002/ajmg.a.37795 |
0.38 |
|
| 2016 |
Gruhn JR, Al-Asmar N, Fasnacht R, Maylor-Hagen H, Peinado V, Rubio C, Broman KW, Hunt PA, Hassold T. Correlations between Synaptic Initiation and Meiotic Recombination: A Study of Humans and Mice. American Journal of Human Genetics. 98: 102-15. PMID 26749305 DOI: 10.1016/J.Ajhg.2015.11.019 |
0.778 |
|
| 2015 |
Vrooman LA, Oatley JM, Griswold JE, Hassold TJ, Hunt PA. Estrogenic exposure alters the spermatogonial stem cells in the developing testis, permanently reducing crossover levels in the adult. Plos Genetics. 11: e1004949. PMID 25615633 DOI: 10.1371/Journal.Pgen.1004949 |
0.59 |
|
| 2014 |
Rowsey R, Gruhn J, Broman KW, Hunt PA, Hassold T. Examining variation in recombination levels in the human female: a test of the production-line hypothesis. American Journal of Human Genetics. 95: 108-12. PMID 24995869 DOI: 10.1097/Ogx.0000000000000135 |
0.781 |
|
| 2014 |
Baier B, Hunt P, Broman KW, Hassold T. Variation in genome-wide levels of meiotic recombination is established at the onset of prophase in mammalian males. Plos Genetics. 10: e1004125. PMID 24497841 DOI: 10.1371/Journal.Pgen.1004125 |
0.596 |
|
| 2014 |
Vrooman LA, Nagaoka SI, Hassold TJ, Hunt PA. Evidence for paternal age-related alterations in meiotic chromosome dynamics in the mouse. Genetics. 196: 385-96. PMID 24318536 DOI: 10.1534/Genetics.113.158782 |
0.579 |
|
| 2013 |
Gruhn JR, Rubio C, Broman KW, Hunt PA, Hassold T. Cytological studies of human meiosis: sex-specific differences in recombination originate at, or prior to, establishment of double-strand breaks. Plos One. 8: e85075. PMID 24376867 DOI: 10.1371/Journal.Pone.0085075 |
0.792 |
|
| 2013 |
Rowsey R, Kashevarova A, Murdoch B, Dickenson C, Woodruff T, Cheng E, Hunt P, Hassold T. Germline mosaicism does not explain the maternal age effect on trisomy. American Journal of Medical Genetics. Part A. 161: 2495-503. PMID 23950106 DOI: 10.1002/Ajmg.A.36120 |
0.664 |
|
| 2013 |
Murdoch B, Owen N, Stevense M, Smith H, Nagaoka S, Hassold T, McKay M, Xu H, Fu J, Revenkova E, Jessberger R, Hunt P. Altered cohesin gene dosage affects Mammalian meiotic chromosome structure and behavior. Plos Genetics. 9: e1003241. PMID 23408896 DOI: 10.1371/Journal.Pgen.1003241 |
0.651 |
|
| 2013 |
Johnson ME, Rowsey RA, Shirley S, Vandevoort C, Bailey J, Hassold T. A specific family of interspersed repeats (SINEs) facilitates meiotic synapsis in mammals. Molecular Cytogenetics. 6: 1. PMID 23276256 DOI: 10.1186/1755-8166-6-1 |
0.419 |
|
| 2012 |
Hunt PA, Lawson C, Gieske M, Murdoch B, Smith H, Marre A, Hassold T, VandeVoort CA. Bisphenol A alters early oogenesis and follicle formation in the fetal ovary of the rhesus monkey. Proceedings of the National Academy of Sciences of the United States of America. 109: 17525-30. PMID 23012422 DOI: 10.1073/Pnas.1207854109 |
0.606 |
|
| 2012 |
Nagaoka SI, Hassold TJ, Hunt PA. Human aneuploidy: mechanisms and new insights into an age-old problem. Nature Reviews. Genetics. 13: 493-504. PMID 22705668 DOI: 10.1038/nrg3245 |
0.546 |
|
| 2012 |
Al-Asmar N, Peinado V, Vera M, Remohà J, Pellicer A, Simón C, Hassold T, Rubio C. Chromosomal abnormalities in embryos from couples with a previous aneuploid miscarriage. Fertility and Sterility. 98: 145-50. PMID 22521156 DOI: 10.1016/J.Fertnstert.2012.03.035 |
0.457 |
|
| 2011 |
Lawson C, Gieske M, Murdoch B, Ye P, Li Y, Hassold T, Hunt PA. Gene expression in the fetal mouse ovary is altered by exposure to low doses of bisphenol A. Biology of Reproduction. 84: 79-86. PMID 20739668 DOI: 10.1095/Biolreprod.110.084814 |
0.586 |
|
| 2011 |
Hassold T. The Origin of Aneuploidy in Humans: Does Prophase Set the Stage? Biology of Reproduction. 85: 166-166. DOI: 10.1093/Biolreprod/85.S1.166 |
0.312 |
|
| 2011 |
Gruhn JR, Broman KW, Hunt PA, Hassold TJ. The embryo/blastomere: Meiotic recombination in human oocytes Stem Cells in Reproductive Medicine: Basic Science and Therapeutic Potential. 63-75. DOI: 10.1017/CBO9781139540742.007 |
0.804 |
|
| 2010 |
Billings T, Sargent EE, Szatkiewicz JP, Leahy N, Kwak IY, Bektassova N, Walker M, Hassold T, Graber JH, Broman KW, Petkov PM. Patterns of recombination activity on mouse chromosome 11 revealed by high resolution mapping. Plos One. 5: e15340. PMID 21170346 DOI: 10.1371/Journal.Pone.0015340 |
0.505 |
|
| 2010 |
Murdoch B, Owen N, Shirley S, Crumb S, Broman KW, Hassold T. Multiple loci contribute to genome-wide recombination levels in male mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 550-5. PMID 21113599 DOI: 10.1007/S00335-010-9303-5 |
0.449 |
|
| 2010 |
Hunt P, Hassold T. Female meiosis: coming unglued with age. Current Biology : Cb. 20: R699-702. PMID 20833308 DOI: 10.1016/J.Cub.2010.08.011 |
0.642 |
|
| 2010 |
Zheng P, Griswold MD, Hassold TJ, Hunt PA, Small CL, Ye P. Predicting meiotic pathways in human fetal oogenesis. Biology of Reproduction. 82: 543-51. PMID 19846598 DOI: 10.1095/Biolreprod.109.079590 |
0.479 |
|
| 2010 |
Hassold T. 2009 William Allan Award Introduction: Huntington F. Willard American Journal of Human Genetics. 86: 316-317. DOI: 10.1016/J.Ajhg.2010.01.003 |
0.357 |
|
| 2009 |
Hassold T, Hunt P. Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew. Current Opinion in Pediatrics. 21: 703-8. PMID 19881348 DOI: 10.1097/MOP.0b013e328332c6ab |
0.522 |
|
| 2009 |
Cheng EY, Hunt PA, Naluai-Cecchini TA, Fligner CL, Fujimoto VY, Pasternack TL, Schwartz JM, Steinauer JE, Woodruff TJ, Cherry SM, Hansen TA, Vallente RU, Broman KW, Hassold TJ. Meiotic recombination in human oocytes. Plos Genetics. 5: e1000661. PMID 19763179 DOI: 10.1371/Journal.Pgen.1000661 |
0.634 |
|
| 2009 |
Hunt PA, Susiarjo M, Rubio C, Hassold TJ. The bisphenol A experience: a primer for the analysis of environmental effects on mammalian reproduction. Biology of Reproduction. 81: 807-13. PMID 19458313 DOI: 10.1095/biolreprod.109.077008 |
0.485 |
|
| 2009 |
Hassold T, Hansen T, Hunt P, Vandevoort C. Cytological studies of recombination in rhesus males Cytogenetic and Genome Research. 124: 132-138. PMID 19420925 DOI: 10.1159/000207519 |
0.666 |
|
| 2009 |
Houmard B, Small C, Yang L, Naluai-Cecchini T, Cheng E, Hassold T, Griswold M. Global gene expression in the human fetal testis and ovary. Biology of Reproduction. 81: 438-43. PMID 19369649 DOI: 10.1095/Biolreprod.108.075747 |
0.347 |
|
| 2009 |
Myers JP, vom Saal FS, Akingbemi BT, Arizono K, Belcher S, Colborn T, Chahoud I, Crain DA, Farabollini F, Guillette LJ, Hassold T, Ho SM, Hunt PA, Iguchi T, Jobling S, et al. Why public health agencies cannot depend on good laboratory practices as a criterion for selecting data: the case of bisphenol A. Environmental Health Perspectives. 117: 309-15. PMID 19337501 DOI: 10.1289/Ehp.0800173 |
0.424 |
|
| 2009 |
Muhlhauser A, Susiarjo M, Rubio C, Griswold J, Gorence G, Hassold T, Hunt PA. Bisphenol A effects on the growing mouse oocyte are influenced by diet. Biology of Reproduction. 80: 1066-71. PMID 19164168 DOI: 10.1095/Biolreprod.108.074815 |
0.599 |
|
| 2009 |
Hunt PA, Hassold T. BPA: traditional toxicology testing is inadequate and concerns extend beyond aneuploidy Trends in Genetics. 25: 15-16. DOI: 10.1016/J.Tig.2008.10.006 |
0.586 |
|
| 2008 |
Anderson EL, Baltus AE, Roepers-Gajadien HL, Hassold TJ, de Rooij DG, van Pelt AM, Page DC. Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice. Proceedings of the National Academy of Sciences of the United States of America. 105: 14976-80. PMID 18799751 DOI: 10.1073/Pnas.0807297105 |
0.352 |
|
| 2008 |
Hunt PA, Hassold TJ. Human female meiosis: what makes a good egg go bad? Trends in Genetics : Tig. 24: 86-93. PMID 18192063 DOI: 10.1016/j.tig.2007.11.010 |
0.557 |
|
| 2008 |
Hassold T, Naluai-Cecchini T, Cherry S, Hansen T, Cheng E. Cytogenetic Studies of Meiotic Recombination in Human Females. Biology of Reproduction. 78: 192-192. DOI: 10.1093/Biolreprod/78.S1.192A |
0.471 |
|
| 2007 |
Hassold T, Hall H, Hunt P. The origin of human aneuploidy: where we have been, where we are going. Human Molecular Genetics. 16: R203-8. PMID 17911163 DOI: 10.1093/Hmg/Ddm243 |
0.726 |
|
| 2007 |
Hassold T, Hunt P. Rescuing distal crossovers. Nature Genetics. 39: 1187-8. PMID 17898774 DOI: 10.1038/Ng1007-1187 |
0.586 |
|
| 2007 |
Hall HE, Chan ER, Collins A, Judis L, Shirley S, Surti U, Hoffner L, Cockwell AE, Jacobs PA, Hassold TJ. The origin of trisomy 13. American Journal of Medical Genetics. Part A. 143: 2242-8. PMID 17853475 DOI: 10.1002/Ajmg.A.31913 |
0.64 |
|
| 2007 |
Hall HE, Surti U, Hoffner L, Shirley S, Feingold E, Hassold T. The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction. American Journal of Medical Genetics. Part A. 143: 2249-55. PMID 17705154 DOI: 10.1002/Ajmg.A.31918 |
0.68 |
|
| 2007 |
Cherry SM, Adelman CA, Theunissen JW, Hassold TJ, Hunt PA, Petrini JH. The Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosis. Current Biology : Cb. 17: 373-8. PMID 17291760 DOI: 10.1016/J.Cub.2006.12.048 |
0.556 |
|
| 2007 |
Susiarjo M, Hassold TJ, Freeman E, Hunt PA. Bisphenol A exposure in utero disrupts early oogenesis in the mouse. Plos Genetics. 3: e5. PMID 17222059 DOI: 10.1371/journal.pgen.0030005 |
0.567 |
|
| 2007 |
Topping D, Brown P, Hassold T. The immunocytogenetics of human male meiosis: A progress report The Genetics of Male Infertility. 115-128. DOI: 10.1007/978-1-59745-176-5_7 |
0.421 |
|
| 2006 |
Koehler KE, Schrump SE, Cherry JP, Hassold TJ, Hunt PA. Near-human aneuploidy levels in female mice with homeologous chromosomes. Current Biology : Cb. 16: R579-80. PMID 16890511 DOI: 10.1016/j.cub.2006.07.018 |
0.617 |
|
| 2006 |
Topping D, Brown P, Judis L, Schwartz S, Seftel A, Thomas A, Hassold T. Synaptic defects at meiosis I and non-obstructive azoospermia. Human Reproduction (Oxford, England). 21: 3171-7. PMID 16861745 DOI: 10.1093/Humrep/Del281 |
0.302 |
|
| 2006 |
Hall H, Hunt P, Hassold T. Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors. Current Opinion in Genetics & Development. 16: 323-9. PMID 16647844 DOI: 10.1016/J.Gde.2006.04.011 |
0.756 |
|
| 2006 |
Cheng E, Vallente R, Diperna D, Naluai-Cecchini T, Hassold T. Direct analysis of meiotic recombination in human trisomy 18 oocytes American Journal of Obstetrics and Gynecology. 195: S175. DOI: 10.1016/J.Ajog.2006.10.622 |
0.523 |
|
| 2005 |
Hodges CA, Revenkova E, Jessberger R, Hassold TJ, Hunt PA. SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction. Nature Genetics. 37: 1351-5. PMID 16258540 DOI: 10.1038/ng1672 |
0.627 |
|
| 2005 |
Lamb NE, Sherman SL, Hassold TJ. Effect of meiotic recombination on the production of aneuploid gametes in humans Cytogenetic and Genome Research. 111: 250-255. PMID 16192701 DOI: 10.1159/000086896 |
0.418 |
|
| 2005 |
Lynn A, Schrump S, Cherry J, Hassold T, Hunt P. Sex, not genotype, determines recombination levels in mice. American Journal of Human Genetics. 77: 670-5. PMID 16175513 DOI: 10.1086/491718 |
0.672 |
|
| 2005 |
Brown PW, Judis L, Chan ER, Schwartz S, Seftel A, Thomas A, Hassold TJ. Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human male. American Journal of Human Genetics. 77: 556-66. PMID 16175502 DOI: 10.1086/468188 |
0.406 |
|
| 2004 |
Cherry SM, Hunt PA, Hassold TJ. Cisplatin disrupts mammalian spermatogenesis, but does not affect recombination or chromosome segregation. Mutation Research. 564: 115-28. PMID 15507376 DOI: 10.1016/j.mrgentox.2004.08.010 |
0.562 |
|
| 2004 |
Lynn A, Ashley T, Hassold T. Variation in human meiotic recombination. Annual Review of Genomics and Human Genetics. 5: 317-49. PMID 15485352 DOI: 10.1146/Annurev.Genom.4.070802.110217 |
0.397 |
|
| 2004 |
Hassold T, Judis L, Chan ER, Schwartz S, Seftel A, Lynn A. Cytological studies of meiotic recombination in human males Cytogenetic and Genome Research. 107: 249-255. PMID 15467369 DOI: 10.1159/000080602 |
0.48 |
|
| 2004 |
Koehler KE, Millie EA, Cherry JP, Schrump SE, Hassold TJ. Meiotic exchange and segregation in female mice heterozygous for paracentric inversions. Genetics. 166: 1199-214. PMID 15082541 DOI: 10.1534/genetics.166.3.1199 |
0.365 |
|
| 2004 |
Judis L, Chan ER, Schwartz S, Seftel A, Hassold T. Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex. Fertility and Sterility. 81: 205-9. PMID 14711569 DOI: 10.1016/J.Fertnstert.2003.05.021 |
0.356 |
|
| 2004 |
Hassold T, Pettay D, May K, Robinson A. Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy Human Genetics. 85: 648-650. PMID 1977687 DOI: 10.1007/Bf00193591 |
0.464 |
|
| 2004 |
Hassold T, Pettay D, Robinson A, Uchida I. Molecular studies of parental origin and mosaicism in 45,X conceptuses Human Genetics. 89: 647-652. PMID 1511983 DOI: 10.1007/Bf00221956 |
0.367 |
|
| 2003 |
Koehler KE, Voigt RC, Thomas S, Lamb B, Urban C, Hassold T, Hunt PA. When disaster strikes: rethinking caging materials. Lab Animal. 32: 24-7. PMID 19753748 DOI: 10.1038/Laban0403-24 |
0.471 |
|
| 2003 |
Thomas NS, Hassold TJ. Aberrant recombination and the origin of Klinefelter syndrome Human Reproduction Update. 9: 309-317. PMID 12926525 DOI: 10.1093/humupd/dmg028 |
0.416 |
|
| 2003 |
Hunt PA, Koehler KE, Susiarjo M, Hodges CA, Ilagan A, Voigt RC, Thomas S, Thomas BF, Hassold TJ. Bisphenol a exposure causes meiotic aneuploidy in the female mouse. Current Biology : Cb. 13: 546-53. PMID 12676084 DOI: 10.1016/S0960-9822(03)00189-1 |
0.55 |
|
| 2002 |
Koehler KE, Millie EA, Cherry JP, Burgoyne PS, Evans EP, Hunt PA, Hassold TJ. Sex-specific differences in meiotic chromosome segregation revealed by dicentric bridge resolution in mice. Genetics. 162: 1367-79. PMID 12454080 |
0.624 |
|
| 2002 |
Koehler KE, Cherry JP, Lynn A, Hunt PA, Hassold TJ. Genetic control of mammalian meiotic recombination. I. Variation in exchange frequencies among males from inbred mouse strains. Genetics. 162: 297-306. PMID 12242241 |
0.527 |
|
| 2002 |
Bean CJ, Hassold TJ, Judis L, Hunt PA. Fertilization in vitro increases non-disjunction during early cleavage divisions in a mouse model system. Human Reproduction (Oxford, England). 17: 2362-7. PMID 12202426 |
0.598 |
|
| 2002 |
Hunt PA, Hassold TJ. Sex matters in meiosis. Science (New York, N.Y.). 296: 2181-3. PMID 12077403 DOI: 10.1126/science.1071907 |
0.529 |
|
| 2002 |
Lynn A, Koehler KE, Judis L, Chan ER, Cherry JP, Schwartz S, Seftel A, Hunt PA, Hassold TJ. Covariation of synaptonemal complex length and mammalian meiotic exchange rates. Science (New York, N.Y.). 296: 2222-5. PMID 12052900 DOI: 10.1126/science.1071220 |
0.517 |
|
| 2001 |
Bean CJ, Hunt PA, Millie EA, Hassold TJ. Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone. Human Molecular Genetics. 10: 963-72. PMID 11309370 |
0.622 |
|
| 2001 |
Hassold T, Hunt P. To err (meiotically) is human: The genesis of human aneuploidy Nature Reviews Genetics. 2: 280-291. PMID 11283700 DOI: 10.1038/35066065 |
0.567 |
|
| 2001 |
Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA. Maternal sex chromosome non-disjunction: Evidence for X chromosome-specific risk factors Human Molecular Genetics. 10: 243-250. PMID 11159943 |
0.428 |
|
| 2000 |
Thomas NS, Collins AR, Hassold TJ, Jacobs PA. A reinvestigation of non-disjunction resulting in 47, XXY males of paternal origin. European Journal of Human Genetics : Ejhg. 8: 805-8. PMID 11039584 DOI: 10.1038/sj.ejhg.5200531 |
0.328 |
|
| 2000 |
Hassold T, Sherman S, Hunt P. Counting cross-overs: Characterizing meiotic recombination in mammals Human Molecular Genetics. 9: 2409-2419. PMID 11005796 DOI: 10.1093/Hmg/9.16.2409 |
0.563 |
|
| 2000 |
LePage DF, Church DM, Millie E, Hassold TJ, Conlon RA. Rapid generation of nested chromosomal deletions on mouse chromosome 2. Proceedings of the National Academy of Sciences of the United States of America. 97: 10471-6. PMID 10984539 DOI: 10.1073/Pnas.97.19.10471 |
0.357 |
|
| 2000 |
Robinson WP, Christian SL, Kuchinka BD, Peñaherrera MS, Das S, Schuffenhauer S, Malcolm S, Schinzel AA, Hassold TJ, Ledbetter DH. Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15 Clinical Genetics. 57: 349-358. PMID 10852369 DOI: 10.1034/J.1399-0004.2000.570505.X |
0.412 |
|
| 2000 |
Hassold T, Sherman S. Down syndrome: Genetic recombination and the origin of the extra chromosome 21 Clinical Genetics. 57: 95-100. PMID 10735628 DOI: 10.1034/J.1399-0004.2000.570201.X |
0.488 |
|
| 1999 |
Mroz K, Hassold TJ, Hunt PA. Meiotic aneuploidy in the XXY mouse: Evidence that a compromised testicular environment increases the incidence of meiotic errors Human Reproduction. 14: 1151-1156. PMID 10325252 DOI: 10.1093/humrep/14.5.1151 |
0.594 |
|
| 1999 |
Redline RW, Zaragoza M, Hassold T. Prevalence of developmental and inflammatory lesions in nonmolar first- trimester spontaneous abortions Human Pathology. 30: 93-100. PMID 9923934 DOI: 10.1016/S0046-8177(99)90307-6 |
0.321 |
|
| 1998 |
Koehler KE, Hassold TJ. Human aneuploidy: Lessons from achiasmate segregation in Drosophila melanogaster Annals of Human Genetics. 62: 467-479. PMID 10363125 DOI: 10.1017/S0003480098007179 |
0.452 |
|
| 1998 |
Hixon M, Millie E, Judis LA, Sherman S, Allran K, Taft L, Hassold T. FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy. Human Genetics. 103: 654-7. PMID 9921898 DOI: 10.1007/S004390050886 |
0.43 |
|
| 1998 |
Shaffer LG, McCaskill C, Adkins K, Hassold TJ. Systematic search for uniparental disomy in early fetal losses: the results and a review of the literature. American Journal of Medical Genetics. 79: 366-72. PMID 9779803 DOI: 10.1002/(SICI)1096-8628(19981012)79:5<366::AID-AJMG7>3.0.CO;2-H |
0.348 |
|
| 1998 |
Redline RW, Hassold T, Zaragoza M. Determinants of villous trophoblastic hyperplasia in spontaneous abortions Modern Pathology. 11: 762-768. PMID 9720505 |
0.329 |
|
| 1998 |
Savage AR, Petersen MB, Pettay D, Taft L, Allran K, Freeman SB, Karadima G, Avramopoulos D, Torfs C, Mikkelsen M, Hassold TJ, Sherman SL. Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans. Human Molecular Genetics. 7: 1221-7. PMID 9668162 |
0.341 |
|
| 1998 |
Shen JJ, Sherman SL, Hassold TJ. Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome Chromosoma. 107: 166-172. PMID 9639654 DOI: 10.1007/s004120050293 |
0.391 |
|
| 1998 |
Redline RW, Hassold T, Zaragoza MV. Prevalence of the partial molar phenotype in triploidy of maternal and paternal origin Human Pathology. 29: 505-511. PMID 9596275 DOI: 10.1016/S0046-8177(98)90067-3 |
0.309 |
|
| 1998 |
Robinson WP, Kuchinka BD, Bernasconi F, Petersen MB, Schulze A, Brondum-Nielsen K, Christian SL, Ledbetter DH, Schinzel AA, Horsthemke B, Schuffenhauer S, Michaelis RC, Langlois S, Hassold TJ. Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination. Human Molecular Genetics. 7: 1011-9. PMID 9580665 DOI: 10.1093/Hmg/7.6.1011 |
0.38 |
|
| 1997 |
O'Keefe CL, Griffin DK, Bean CJ, Matera AG, Hassold TJ. Alphoid variant-specific FISH probes can distinguish autosomal meiosis I from meiosis II non-disjunction in human sperm. Human Genetics. 101: 61-6. PMID 9385371 DOI: 10.1007/S004390050587 |
0.384 |
|
| 1997 |
Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, ... Hassold T, et al. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21 Human Molecular Genetics. 6: 1391-1399. PMID 9285774 DOI: 10.1093/Hmg/6.9.1391 |
0.439 |
|
| 1997 |
Zaragoza MV, Keep D, Genest DR, Hassold T, Redline RW. Early complete hydatidiform moles contain inner cell mass derivatives. American Journal of Medical Genetics. 70: 273-7. PMID 9188665 DOI: 10.1002/(Sici)1096-8628(19970613)70:3<273::Aid-Ajmg11>3.0.Co;2-I |
0.301 |
|
| 1996 |
Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, Gu Y, Shen J, Saker D, May KM, Avramopoulos D, Petersen MB, Hallberg A, Mikkelsen M, Hassold TJ, et al. Susceptible chiasmate configurations of chromosome 21 predispose to non- disjunction in both maternal meiosis I and meiosis II Nature Genetics. 14: 400-405. PMID 8944019 DOI: 10.1038/ng1296-400 |
0.344 |
|
| 1996 |
Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M, Millie E, Saker D, Shen J, Zaragoza M. Human aneuploidy: incidence, origin, and etiology. Environmental and Molecular Mutagenesis. 28: 167-75. PMID 8908177 DOI: 10.1002/(Sici)1098-2280(1996)28:3<167::Aid-Em2>3.0.Co;2-B |
0.489 |
|
| 1996 |
Bishop JB, Dellarco VL, Hassold T, Ferguson LR, Wyrobek AJ, Friedman JM. Aneuploidy in germ cells: etiologies and risk factors. Environmental and Molecular Mutagenesis. 28: 159-66. PMID 8908176 DOI: 10.1002/(Sici)1098-2280(1996)28:3<159::Aid-Em1>3.0.Co;2-9 |
0.423 |
|
| 1996 |
Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ. Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. American Journal of Human Genetics. 59: 1108-13. PMID 8900240 |
0.398 |
|
| 1996 |
Koehler KE, Hawley RS, Sherman S, Hassold T. Recombination and nondisjunction in humans and flies. Human Molecular Genetics. 5: 1495-504. PMID 8875256 DOI: 10.1093/Hmg/5.Supplement_1.1495 |
0.436 |
|
| 1996 |
Keep D, Zaragoza MV, Hassold T, Redline RW. Very early complete hydatidiform mole Human Pathology. 27: 708-713. PMID 8698316 DOI: 10.1016/S0046-8177(96)90402-5 |
0.324 |
|
| 1996 |
Abruzzo MA, Griffin DK, Millie EA, Sheean LA, Hassold TJ. The effect of Y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm Human Genetics. 97: 819-823. PMID 8641703 DOI: 10.1007/s004390050143 |
0.403 |
|
| 1995 |
Abruzzo MA, Hassold TJ. Etiology of nondisjunction in humans Environmental and Molecular Mutagenesis. 25: 38-47. PMID 7789361 DOI: 10.1002/em.2850250608 |
0.447 |
|
| 1995 |
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. American Journal of Human Genetics. 57: 867-74. PMID 7573048 |
0.397 |
|
| 1995 |
Jacobs PA, Hassold TJ. 4 The Origin of Numerical Chromosome Abnormalities Advances in Genetics. 33: 101-133. PMID 7484451 DOI: 10.1016/S0065-2660(08)60332-6 |
0.345 |
|
| 1994 |
James RS, Temple IK, Patch C, Thompson EM, Hassold T, Jacobs PA. A systematic search for uniparental disomy in carriers of chromosome translocations. European Journal of Human Genetics : Ejhg. 2: 83-95. PMID 8044660 |
0.345 |
|
| 1994 |
Macdonald M, Hassold T, Harvey J, Wang LH, Morton NE, Jacobs P. The origin of 47, XXY and 47, XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination Human Molecular Genetics. 3: 1365-1371. PMID 7987316 DOI: 10.1093/Hmg/3.8.1365 |
0.492 |
|
| 1994 |
Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns Human Genetics. 94: 411-417. PMID 7927339 DOI: 10.1007/Bf00201603 |
0.471 |
|
| 1994 |
Sherman SL, Petersen MB, Freeman SB, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold TJ. Non-disjunction of chromosome 21 in maternal meiosis I: Evidence for a maternal age-dependent mechanism involving reduced recombination Human Molecular Genetics. 3: 1529-1535. PMID 7833907 DOI: 10.1093/hmg/3.9.1529 |
0.332 |
|
| 1993 |
Hassold T, Hunt PA, Sherman S. Trisomy in humans: incidence, origin and etiology Current Opinion in Genetics and Development. 3: 398-403. PMID 8353412 DOI: 10.1016/0959-437X(93)90111-2 |
0.582 |
|
| 1993 |
Williams BJ, Ballenger CA, Malter HE, Bishop F, Tucker M, Zwingman TA, Hassold TJ. Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes. Human Molecular Genetics. 2: 1929-36. PMID 8281157 DOI: 10.1093/hmg/2.11.1929 |
0.407 |
|
| 1993 |
Patersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, Avramopoulos D, Mikkelsen M. Paternal nondisjunction in trisomy 21: Excess of male patients Human Molecular Genetics. 2: 1691-1695. PMID 8268923 DOI: 10.1093/hmg/2.10.1691 |
0.352 |
|
| 1992 |
Krasikov N, Takaesu N, Hassold T, Knops JF, Finley WH, Scarbrough P. Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype. American Journal of Medical Genetics. 43: 554-60. PMID 1605248 DOI: 10.1002/Ajmg.1320430310 |
0.372 |
|
| 1992 |
Lorber BJ, Grantham M, Peters J, Willard HF, Hassold TJ. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. American Journal of Human Genetics. 51: 1265-76. PMID 1463010 |
0.326 |
|
| 1992 |
Lorber BJ, Freeman SB, Hassold T, Ragab AH, Vega RA, Cockwell AE, Jacobs PA, Radford M, Doyle J, Dubé ID. Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia. Genes, Chromosomes & Cancer. 4: 222-7. PMID 1382563 DOI: 10.1002/Gcc.2870040306 |
0.361 |
|
| 1992 |
Takaesu N, Newfeld S, Hassold T. Characterization of three VNTR systems at D21S112 Genomics. 14: 816-817. PMID 1339394 DOI: 10.1016/S0888-7543(05)80197-1 |
0.357 |
|
| 1991 |
Hassold TJ, Pettay D, Freeman SB, Grantham M, Takaesu N. Molecular studies of non-disjunction in trisomy 16. Journal of Medical Genetics. 28: 159-62. PMID 2051452 |
0.391 |
|
| 1991 |
Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region American Journal of Human Genetics. 49: 253-260. PMID 1867189 |
0.357 |
|
| 1991 |
Sherman SL, Takaesu N, Freeman SB, Grantham M, Phillips C, Blackston RD, Jacobs PA, Cockwell AE, Freeman V, Uchida I, Mikkelsen M, Kurnit DM, Buraczynska M, Keats BJB, Hassold TJ. Trisomy 21: Association between reduced recombination and nondisjunction American Journal of Human Genetics. 49: 608-620. PMID 1831960 |
0.346 |
|
| 1991 |
Temple IK, Cockwell A, Hassold T, Pettay D, Jacobs P. Maternal uniparental disomy for chromosome 14. Journal of Medical Genetics. 28: 511-4. PMID 1681108 |
0.416 |
|
| 1990 |
May KM, Jacobs PA, Lee M, Ratcliffe S, Robinson A, Nielsen J, Hassold TJ. The parental origin of the extra X chromosome in 47,XXX females. American Journal of Human Genetics. 46: 754-61. PMID 2316522 |
0.334 |
|
| 1990 |
Harvey J, Jacobs PA, Hassold T, Pettay D. The parental origin of 47,XXY males Birth Defects: Original Article Series. 26: 289-296. PMID 2090327 |
0.327 |
|
| 1990 |
Hassold T, Arnovitz K, Jacobs PA, May K, Robinson D. The parental origin of the missing or additional chromosome in 45,X and 47,XXX females Birth Defects: Original Article Series. 26: 297-304. PMID 1982521 |
0.32 |
|
| 1990 |
Takaesu N, Jacobs PA, Cockwell A, Blackston RD, Freeman S, Nuccio J, Kurnit DM, Uchida I, Freeman V, Hassold T. Nondisjunction of chromosome 21. American Journal of Medical Genetics. Supplement. 7: 175-81. PMID 1981476 DOI: 10.1002/Ajmg.1320370735 |
0.438 |
|
| 1990 |
Morton NE, Keats BJ, Jacobs PA, Hassold T, Pettay D, Harvey J, Andrews V. A centromere map of the X chromosome from trisomies of maternal origin Annals of Human Genetics. 54: 39-47. PMID 1969722 DOI: 10.1111/J.1469-1809.1990.Tb00359.X |
0.406 |
|
| 1989 |
Buraczynska M, Stewart GD, Sherman S, Freeman V, Grantham M, Uchida I, Hassold T, Kurnit DM. Studying nondisjunction of chromosome 21 with cytogenetic markers on the short arm and DNA markers encompassing the long arm Progress in Clinical and Biological Research. 311: 101-113. PMID 2570424 |
0.3 |
|
| 1989 |
Jacobs P, Hassold T, Harvey J, May K. The origin of sex chromosome aneuploidy Progress in Clinical and Biological Research. 311: 135-151. PMID 2528150 |
0.401 |
|
| 1988 |
Hassold T, Jacobs PA, Pettay D. Cytogenetic studies of couples with repeated spontaneous abortions of known karyotype Genetic Epidemiology. 5: 65-74. PMID 3402725 |
0.313 |
|
| 1988 |
Jacobs PA, Bacino C, Hassold T, Morton NE, Keston M, Lee M. A cytogenetic study of 47,XXY males of known origin and their parents Annals of Human Genetics. 52: 319-325. PMID 3268043 DOI: 10.1111/J.1469-1809.1988.Tb01111.X |
0.423 |
|
| 1988 |
Morton NE, Jacobs PA, Hassold T, Wu D. Maternal age in trisomy Annals of Human Genetics. 52: 227-235. PMID 2977936 DOI: 10.1111/J.1469-1809.1988.Tb01100.X |
0.363 |
|
| 1988 |
Jacobs PA, Hassold TJ, Whittington E, Butler G, Collyer S, Keston M, Lee M. Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes. Annals of Human Genetics. 52: 93-109. PMID 2907853 |
0.386 |
|
| 1988 |
Hassold T, Benham F, Leppert M. Cytogenetic and molecular analysis of sex-chromosome monosomy. American Journal of Human Genetics. 42: 534-41. PMID 2894760 |
0.336 |
|
| 1988 |
Stewart GD, Hassold TJ, Berg A, Watkins P, Tanzi R, Kurnit DM. Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21. American Journal of Human Genetics. 42: 227-36. PMID 2893544 |
0.312 |
|
| 1987 |
Warburton D, Kline J, Stein Z, Hutzler M, Chin A, Hassold T. Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions. American Journal of Human Genetics. 41: 465-83. PMID 3631080 |
0.304 |
|
| 1987 |
Jacobs PA, Hassold TJ, Henry A, Pettay D, Takaesu N. Trisomy 13 ascertained in a survey of spontaneous abortions. Journal of Medical Genetics. 24: 721-4. PMID 3430552 |
0.338 |
|
| 1987 |
Hassold T, Jacobs PA, Leppert M, Sheldon M. Cytogenetic and molecular studies of trisomy 13. Journal of Medical Genetics. 24: 725-32. PMID 2892938 |
0.303 |
|
| 1986 |
Hassold TJ. Chromosome abnormalities in human reproductive wastage Trends in Genetics. 2: 105-110. DOI: 10.1016/0168-9525(86)90194-0 |
0.408 |
|
| 1985 |
Hassold T, Chiu D. Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomy Human Genetics. 70: 11-17. PMID 3997148 DOI: 10.1007/Bf00389450 |
0.462 |
|
| 1985 |
Hassold T, Kumlin E, Takaesu N, Leppert M. Use of restriction fragment length polymorphisms to study the origin of human aneuploidy Annals of the New York Academy of Sciences. 179-189. PMID 2990309 DOI: 10.1111/J.1749-6632.1985.Tb21492.X |
0.455 |
|
| 1984 |
Hassold T, MacLean C. Temporal changes in chromosome abnormality rate in human spontaneous abortions: Evidence for an association between sex-chromosome monosomy and trisomy 16 Cytogenetics and Cell Genetics. 38: 200-205. PMID 6541559 |
0.401 |
|
| 1984 |
Hassold T, Warburton D, Kline J, Stein Z. The relationship of maternal age and trisomy among trisomic spontaneous abortions. American Journal of Human Genetics. 36: 1349-56. PMID 6517056 |
0.307 |
|
| 1984 |
Hassold TJ, Jacobs PA. Trisomy in man Annual Review of Genetics. 18: 69-97. PMID 6241455 |
0.395 |
|
| 1984 |
Hassold T, Chiu D, Yamane JA. Parental origin of autosomal trisomies Annals of Human Genetics. 48: 129-144. PMID 6234852 DOI: 10.1111/J.1469-1809.1984.Tb01008.X |
0.429 |
|
| 1983 |
Hassold T, Sandison A. The effect of chromosome constitution on growth in culture of human spontaneous abortions Human Genetics. 63: 166-170. PMID 6840759 DOI: 10.1007/Bf00291538 |
0.411 |
|
| 1983 |
Hassold T, Quillen SD, Yamane JA. Sex ratio in spontaneous abortions Annals of Human Genetics. 47: 39-47. PMID 6838169 DOI: 10.1111/J.1469-1809.1983.Tb00968.X |
0.485 |
|
| 1982 |
Hassold T. Mosaic trisomies in human spontaneous abortions Human Genetics. 61: 31-35. PMID 7129422 DOI: 10.1007/BF00291327 |
0.373 |
|
| 1982 |
Morton NE, Hassold TJ, Funkhouser J, McKenna PW, Lew R. Cytogenetic surveillance of spontaneous abortions Cytogenetic and Genome Research. 33: 232-239. PMID 7128213 DOI: 10.1159/000131759 |
0.33 |
|
| 1980 |
Hassold TJ. A cytogenetic study of repeated spontaneous abortions. American Journal of Human Genetics. 32: 723-30. PMID 7424911 |
0.382 |
|
| 1980 |
Hassold T, Chen N, Funkhouser J, Jooss T, Manuel B, Matsuura J, Matsuyama A, Wilson C, Yamane JA, Jacobs PA. A cytogenetic study of 1000 spontaneous abortions Annals of Human Genetics. 44: 151-178. PMID 7316468 DOI: 10.1111/J.1469-1809.1980.Tb00955.X |
0.471 |
|
| 1980 |
Hassold T, Jacobs P, Kline J, Stein Z, Warburton D. Effect of maternal age on autosomal trisomies Annals of Human Genetics. 44: 29-36. PMID 7198887 DOI: 10.1111/J.1469-1809.1980.Tb00943.X |
0.456 |
|
| 1979 |
Wisniewski L, Hassold T, Heffelfinger J, Higgins JV. Cytogenetic and clinical studies in five cases of inv dup(15) Human Genetics. 50: 259-270. PMID 489010 DOI: 10.1007/Bf00399391 |
0.402 |
|
| 1979 |
Hassold T, Matsuyama A. Origin of trisomies in human spontaneous abortions Human Genetics. 46: 285-294. PMID 155642 DOI: 10.1007/BF00273312 |
0.352 |
|
| 1978 |
Hassold TJ, Matsuyama A, Newlands IM, Matsuura JS, Jacobs PA, Manuel B, Tsuei J. A cytogenetic study of spontaneous abortions in Hawaii Annals of Human Genetics. 41: 443-454. PMID 655633 |
0.383 |
|
| 1977 |
Wisniewski L, Purdy G, Hassold T, Wilson C, Bentley K, Hackel E, Higgins JV. An interstitial deletion of chromosome 9 in a girl with multiple congenital anomalies. Journal of Medical Genetics. 14: 455-9. PMID 604498 DOI: 10.1136/Jmg.14.6.455 |
0.414 |
|
| 1976 |
Higgins JV, Wisniewski L, Hassold T, Hackel E, Raeburn RA, Buckton KE, Noades JE, Cook P. Two informative translocations involving chromosome 2 Cytogenetic and Genome Research. 16: 314-316. PMID 975898 DOI: 10.1159/000130619 |
0.415 |
|
| 1976 |
Wisniewski L, Purdy G, Hassold T. The secondary constriction of chromosome 9: deletion and breakage studies Excerpta Med.,Amsterdam,I.C.S.. |
0.355 |
|
| 1976 |
Leonard M, Wisniewski L, Hassold T. A familial 2/4 translocation: cytogenetic and linkage studies Excerpta Med.,Amsterdam,I.C.S.. |
0.318 |
|
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