Rivka L. Glaser, Ph.D. - Publications

Affiliations: 
2004 Johns Hopkins University, Baltimore, MD 
Area:
Genetics

9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2009 Yoon SR, Qin J, Glaser RL, Jabs EW, Wexler NS, Sokol R, Arnheim N, Calabrese P. The ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effect. Plos Genetics. 5: e1000558. PMID 19593369 DOI: 10.1371/Journal.Pgen.1000558  0.703
2006 Wyrobek AJ, Eskenazi B, Young S, Arnheim N, Tiemann-Boege I, Jabs EW, Glaser RL, Pearson FS, Evenson D. Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm. Proceedings of the National Academy of Sciences of the United States of America. 103: 9601-6. PMID 16766665 DOI: 10.1073/Pnas.0506468103  0.667
2006 Glaser RL, Ramsay JP, Morison IM. The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations. Nucleic Acids Research. 34: D29-31. PMID 16381868 DOI: 10.1093/Nar/Gkj101  0.468
2006 Wyrobek AJ, Eskenazi B, Young S, Arnheim N, Tiemann-Boege I, Jabs EW, Glaser RL, Pearson FS, Evenson D. Advancing Age Has Differential Effects on DNA Damage, Chromatin Integrity, Gene Mutations, and Aneuploidies in Sperm Obstetrical & Gynecological Survey. 61: 648-649. DOI: 10.1097/01.Ogx.0000238646.91712.3E  0.642
2004 Glaser RL, Jabs EW. Dear old dad. Science of Aging Knowledge Environment : Sage Ke. 2004: re1. PMID 14736914 DOI: 10.1126/Sageke.2004.3.Re1  0.694
2003 Glaser RL, Broman KW, Schulman RL, Eskenazi B, Wyrobek AJ, Jabs EW. The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. American Journal of Human Genetics. 73: 939-47. PMID 12900791 DOI: 10.1086/378419  0.701
2002 Kelley RI, Kratz LE, Glaser RL, Netzloff ML, Wolf LM, Jabs EW. Abnormal sterol metabolism in a patient with Antley-Bixler syndrome and ambiguous genitalia. American Journal of Medical Genetics. 110: 95-102. PMID 12116245 DOI: 10.1002/Ajmg.10510  0.631
2002 Kelley RI, Kratz LE, Glaser RL, Netzloff ML, Wolf LM, Jabs EW. Erratum: Occurrence of thanatophoric dysplasia type I (R248C) and hypochondroplasia (N540K) mutations in two patients with achondroplasia phenotype (American Journal of Medical Genetics (2001) 104 (277-281)) American Journal of Medical Genetics. 110. DOI: 10.1002/Ajmg.10470  0.579
2000 Glaser RL, Jiang W, Boyadjiev SA, Tran AK, Zachary AA, Van Maldergem L, Johnson D, Walsh S, Oldridge M, Wall SA, Wilkie AO, Jabs EW. Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome. American Journal of Human Genetics. 66: 768-77. PMID 10712195 DOI: 10.1086/302831  0.673
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