| Year |
Citation |
Score |
| 2017 |
Williams LS, Demir Eksi D, Shen Y, Lossie AC, Chorich LP, Sullivan ME, Phillips JA, Erman M, Kim HG, Alper OM, Layman LC. Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families. Fertility and Sterility. PMID 28600106 DOI: 10.1016/J.Fertnstert.2017.05.017 |
0.331 |
|
| 2016 |
Lo CL, Lossie AC, Liang T, Liu Y, Xuei X, Lumeng L, Zhou FC, Muir WM. High Resolution Genomic Scans Reveal Genetic Architecture Controlling Alcohol Preference in Bidirectionally Selected Rat Model. Plos Genetics. 12: e1006178. PMID 27490364 DOI: 10.1371/Journal.Pgen.1006178 |
0.327 |
|
| 2016 |
Chowdhury B, Seetharam A, Wang Z, Liu Y, Lossie AC, Thimmapuram J, Irudayaraj J. A Study of Alterations in DNA Epigenetic Modifications (5mC and 5hmC) and Gene Expression Influenced by Simulated Microgravity in Human Lymphoblastoid Cells. Plos One. 11: e0147514. PMID 26820575 DOI: 10.1371/Journal.Pone.0147514 |
0.303 |
|
| 2012 |
Lossie AC, Lo CL, Baumgarner KM, Cramer MJ, Garner JP, Justice MJ. ENU mutagenesis reveals that Notchless homolog 1 (Drosophila) affects Cdkn1a and several members of the Wnt pathway during murine pre-implantation development. Bmc Genetics. 13: 106. PMID 23231322 DOI: 10.1186/1471-2156-13-106 |
0.571 |
|
| 2011 |
Jiang Z, Lossie AC, Applegate TJ. Evolution of trefoil factor(s): genetic and spatio-temporal expression of trefoil factor 2 in the chicken (Gallus gallus domesticus). Plos One. 6: e22691. PMID 21829480 DOI: 10.1371/Journal.Pone.0022691 |
0.307 |
|
| 2005 |
Lossie AC, Meehan TP, Castillo A, Zheng L, Weiser KC, Strivens MA, Justice MJ. 18th international mouse genome conference. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 471-5. PMID 16151691 DOI: 10.1007/S00335-004-4001-9 |
0.504 |
|
| 2005 |
Lossie AC, Nakamura H, Thomas SE, Justice MJ. Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation. Genetics. 169: 285-99. PMID 15489520 DOI: 10.1534/Genetics.104.034967 |
0.566 |
|
| 2001 |
Boyar FZ, Whitney MM, Lossie AC, Gray BA, Keller KL, Stalker HJ, Zori RT, Geffken G, Mutch J, Edge PJ, Voeller KS, Williams CA, Driscoll DJ. A family with a grand-maternally derived interstitial duplication of proximal 15q. Clinical Genetics. 60: 421-30. PMID 11846734 DOI: 10.1034/J.1399-0004.2001.600604.X |
0.608 |
|
| 2001 |
Lossie AC, Whitney MM, Amidon D, Dong HJ, Chen P, Theriaque D, Hutson A, Nicholls RD, Zori RT, Williams CA, Driscoll DJ. Distinct phenotypes distinguish the molecular classes of Angelman syndrome. Journal of Medical Genetics. 38: 834-45. PMID 11748306 DOI: 10.1136/Jmg.38.12.834 |
0.613 |
|
| 2001 |
Williams CA, Lossie A, Driscoll D. Angelman syndrome: mimicking conditions and phenotypes. American Journal of Medical Genetics. 101: 59-64. PMID 11343340 DOI: 10.1002/Ajmg.1316 |
0.586 |
|
| 1999 |
Lossie AC, Driscoll DJ. Transmission of Angelman syndrome by an affected mother Genetics in Medicine. 1: 262-266. PMID 11258627 DOI: 10.1097/00125817-199909000-00004 |
0.596 |
|
| 1999 |
Smilinich NJ, Day CD, Fitzpatrick GV, Caldwell GM, Lossie AC, Cooper PR, Smallwood AC, Joyce JA, Schofield PN, Reik W, Nicholls RD, Weksberg R, Driscoll DJ, Maher ER, Shows TB, et al. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proceedings of the National Academy of Sciences of the United States of America. 96: 8064-9. PMID 10393948 DOI: 10.1073/Pnas.96.14.8064 |
0.593 |
|
| 1997 |
Watkins-Chow DE, Buckwalter MS, Newhouse MM, Lossie AC, Brinkmeier ML, Camper SA. Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics. 40: 114-22. PMID 9070927 DOI: 10.1006/Geno.1996.4532 |
0.594 |
|
| 1995 |
Gage PJ, Lossie AC, Scarlett LM, Lloyd RV, Camper SA. Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response Endocrinology. 136: 1161-1167. PMID 7867569 DOI: 10.1210/Endo.136.3.7867569 |
0.491 |
|
| 1995 |
Lossie AC, Haugen BR, Wood WM, Camper SA, Gordon DF. Chromosomal localization of the large subunit of mouse replication factor C in the mouse and human Mammalian Genome. 6: 58-59. PMID 7719032 DOI: 10.1007/Bf00350900 |
0.566 |
|
| 1995 |
Roller ML, Lossie AC, Koken MHM, Smit EME, Hagemeijer A, Camper SA. Localization of sequences related to the human RAD6 DNA repair gene on mouse Chromosomes 11 and 13 Mammalian Genome. 6: 305-306. PMID 7613042 DOI: 10.1007/Bf00352425 |
0.557 |
|
| 1994 |
Lossie AC, Vandenbergh DJ, Uhl GR, Camper SA. Localization of the dopamine transporter gene, Dat1, on mouse chromosome 13. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 117-8. PMID 8180472 DOI: 10.1007/Bf00292340 |
0.547 |
|
| 1994 |
Zhu W, Lossie AC, Camper SA, Gumucio DL. Chromosomal localization of the transcription factor YY1 in the mouse and human Mammalian Genome. 5: 234-236. PMID 7912122 DOI: 10.1007/Bf00360552 |
0.478 |
|
| 1994 |
Lossie AC, Eipper BA, Hand TA, Camper SA. Localization of the peptidylglycine alpha-amidating monooxygenase gene (Pam) introduces a region of homology between human chromosome 5q and mouse chromosome 1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 738-9. PMID 7873888 DOI: 10.1007/Bf00426085 |
0.599 |
|
| 1993 |
Lossie AC, Buckwalter MS, Camper SA. Lysyl oxidase (Lox) maps between Grl-1 and Adrb-2 on mouse chromosome 18. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 177-8. PMID 8094989 DOI: 10.1007/Bf00352234 |
0.563 |
|
| 1993 |
Lossie AC, Gordon DF, Camper SA. Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse Chromosome 15 Mammalian Genome. 4: 621-623. PMID 7903570 DOI: 10.1007/Bf00361398 |
0.516 |
|
| 1992 |
Buckwalter MS, Lossie AC, Scarlett LM, Camper SA. Localization of the human chromosome 5q genes Gabra-1, Gabrg-2, Il-4, Il-5, and Irf-1 on mouse chromosome 11. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 604-7. PMID 1358285 DOI: 10.1007/Bf00350629 |
0.564 |
|
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