| Year |
Citation |
Score |
| 2014 |
Sayedian F, Senft JR, Spruill MD, Wenger SL, Vos JA. c-MYC Amplification in Acute Myelogenous Leukemia Evolving from Double Minutes (dmins) to Homogeneously Staining Region (hsr). Journal of the Association of Genetic Technologists. 40: 64-7. PMID 26029796 |
0.721 |
|
| 2014 |
Jajosky AN, Coad JE, Vos JA, Martin KH, Senft JR, Wenger SL, Gibson LF. RepSox slows decay of CD34+ acute myeloid leukemia cells and decreases T cell immunoglobulin mucin-3 expression. Stem Cells Translational Medicine. 3: 836-48. PMID 24855276 DOI: 10.5966/Sctm.2013-0193 |
0.665 |
|
| 2014 |
Wenger SL, Hansroth J, Shackelford AL. Decreased telomere length in metaphase and interphase cells from newborns with trisomy 21. Gene. 542: 87. PMID 24630967 DOI: 10.1016/j.gene.2014.03.019 |
0.346 |
|
| 2013 |
Shackelford AL, Conlin LK, Hummel M, Spinner NB, Wenger SL. Persistent mosaicism for 12p duplication/triplication chromosome structural abnormality in peripheral blood. Case Reports in Genetics. 2013: 857926. PMID 24151566 DOI: 10.1155/2013/857926 |
0.449 |
|
| 2012 |
Esan OA, Senft JR, Wenger SL. Patterns of BCR/ABL Gene Rearrangements in Chronic Myeloid Leukemia with Complex t(9;22) Using Fluorescence In Situ Hybridization (FISH). Journal of the Association of Genetic Technologists. 38: 5-7. PMID 22421568 |
0.723 |
|
| 2009 |
Wise JL, Crout RJ, McNeil DW, Weyant RJ, Marazita ML, Wenger SL. Human telomere length correlates to the size of the associated chromosome arm. Plos One. 4: e6013. PMID 19547752 DOI: 10.1371/Journal.Pone.0006013 |
0.723 |
|
| 2009 |
Wise JL, Crout RJ, McNeil DW, Weyant RJ, Marazita ML, Wenger SL. Cryptic subtelomeric rearrangements and X chromosome mosaicism: a study of 565 apparently normal individuals with fluorescent in situ hybridization. Plos One. 4: e5855. PMID 19516895 DOI: 10.1371/Journal.Pone.0005855 |
0.725 |
|
| 2007 |
Wiltshire T, Senft J, Wang Y, Konat GW, Wenger SL, Reed E, Wang W. BRCA1 contributes to cell cycle arrest and chemoresistance in response to the anticancer agent irofulven. Molecular Pharmacology. 71: 1051-60. PMID 17229870 DOI: 10.1124/Mol.106.029504 |
0.701 |
|
| 2006 |
Wang Y, Wiltshire T, Senft J, Wenger SL, Reed E, Wang W. Fanconi anemia D2 protein confers chemoresistance in response to the anticancer agent, irofulven. Molecular Cancer Therapeutics. 5: 3153-61. PMID 17172419 DOI: 10.1158/1535-7163.Mct-06-0427 |
0.684 |
|
| 2005 |
Tang W, Wenger SL. Cell death as a possible mechanism for tissue limited mosaicism in Pallister-Killian syndrome. Journal of the Association of Genetic Technologists. 31: 168-9. PMID 16354943 |
0.364 |
|
| 2005 |
Yu M, Obringer AC, Fowler MH, Hummel M, Wenger SL. Prenatal detection of deletion 6q13q15 in a complex karyotype. Prenatal Diagnosis. 25: 1084-7. PMID 16231325 DOI: 10.1002/pd.1265 |
0.307 |
|
| 2005 |
Jeffries AR, Curran S, Elmslie F, Sharma A, Wenger S, Hummel M, Powell J. Molecular and phenotypic characterization of ring chromosome 22. American Journal of Medical Genetics. Part A. 137: 139-47. PMID 16059935 DOI: 10.1002/Ajmg.A.30780 |
0.492 |
|
| 2004 |
Wenger SL, Senft JR, Sargent LM, Bamezai R, Bairwa N, Grant SG. Comparison of established cell lines at different passages by karyotype and comparative genomic hybridization. Bioscience Reports. 24: 631-9. PMID 16158200 DOI: 10.1007/s10540-005-2797-5 |
0.715 |
|
| 2004 |
Harris DL, Siu BL, Hummel M, Harbert K, Senft J, Sargent L, Wenger SL. Mosaic ring 12p and total anomalous pulmonary venous return. American Journal of Medical Genetics. Part A. 131: 91-3. PMID 15389698 DOI: 10.1002/ajmg.a.30315 |
0.698 |
|
| 2004 |
Wenger SL, Bleigh OC, Hummel M. Cleft palate in a newborn with duplication 2(q13q23). The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 41: 568-70. PMID 15352858 DOI: 10.1597/03-059.1 |
0.384 |
|
| 2004 |
Wang X, Ahmed I, Ericson S, Wenger S. Multiple Chromosome Abnormalities Following Bone Marrow Transplant for Chronic Myelogenous Leukemia. Journal of the Association of Genetic Technologists. 30: 7-9. PMID 15340178 |
0.346 |
|
| 2003 |
Hulley BJ, Hummel M, Wenger SL. Screening for cryptic chromosomal abnormalities in patients with mental retardation and dysmorphic facial features using telomere FISH probes. American Journal of Medical Genetics. Part A. 117: 302-3. PMID 12599198 DOI: 10.1002/ajmg.a.10925 |
0.351 |
|
| 2003 |
Hulley BJ, Hummel M, Cook LL, Boyd BK, Wenger SL. Trisomy 8 mosaicism: selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cells. American Journal of Medical Genetics. Part A. 116: 144-6. PMID 12494432 DOI: 10.1002/ajmg.a.10651 |
0.326 |
|
| 2002 |
Kurian S, Hogan TF, Bleigh OC, Dowdy YG, Merghoub T, Pandolfi PP, Wenger SL. Atypical t(15;17)(q13;q12) in a patient with all-trans retinoic acid refractory secondary acute promyelocytic leukemia: a case report and review of the literature. Cancer Genetics and Cytogenetics. 138: 143-8. PMID 12505260 DOI: 10.1016/S0165-4608(02)00591-5 |
0.395 |
|
| 2001 |
Wenger SL, Orlando SJ. Spontaneous chromosome breakage in pernicious anemia. Clinical Nutrition (Edinburgh, Scotland). 19: 467-8. PMID 11104600 DOI: 10.1054/CLNU.2000.0152 |
0.451 |
|
| 2000 |
Grant SG, Wenger SL, Latimer JJ, Thull D, Burke LW. Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome Clinical Genetics. 58: 209-215. PMID 11076043 DOI: 10.1034/J.1399-0004.2000.580308.X |
0.327 |
|
| 2000 |
Ndah BV, Stead JA, Brancazio LR, Hummel M, Wenger SL. Prenatal detection of trisomy for the entire long arm of chromosome 7. Journal of Medical Genetics. 37: 551-3. PMID 10970193 DOI: 10.1136/jmg.37.7.551 |
0.387 |
|
| 2000 |
Cutenese C, Mullett M, Hummel M, Wenger SL. Ring chromosome 1 in a newborn. Clinical Dysmorphology. 9: 131-3. PMID 10826627 DOI: 10.1097/00019605-200009020-00012 |
0.413 |
|
| 2000 |
Wenger SL, Boone LY, Cummins JH, Del Vecchio MA, Bay CA, Hummel M, Mowery-Rushton PA. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s. American Journal of Medical Genetics. 91: 351-4. PMID 10766997 DOI: 10.1002/(SICI)1096-8628(20000424)91:5<351::AID-AJMG6>3.0.CO;2-A |
0.367 |
|
| 1997 |
Witchel SF, Wenger SL, Hoffman EP. Molecular and cytogenetic studies of X inactivation in a patient with 46,X,del(X)(q22). Journal of Pediatric and Adolescent Gynecology. 10: 78-82. PMID 9179806 DOI: 10.1016/S1083-3188(97)70055-X |
0.366 |
|
| 1997 |
Wenger SL, Sell SL, Painter MJ, Steele MW. Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes. American Journal of Medical Genetics. 70: 150-4. PMID 9128934 DOI: 10.1002/(SICI)1096-8628(19970516)70:2<150::AID-AJMG9>3.0.CO;2-1 |
0.435 |
|
| 1996 |
Greally JM, Neiswanger K, Cummins JH, Boone LY, Lenkey SG, Wenger SL, Lewis JL, Fischer D, Paul RA, Steele MW. A molecular anatomical analysis of mosaic trisomy 16. Human Genetics. 98: 86-90. PMID 8682514 DOI: 10.1007/S004390050165 |
0.424 |
|
| 1995 |
Kocova M, Siegel SF, Wenger SL, Lee PA, Nalesnik M, Trucco M. Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH). American Journal of Medical Genetics. 55: 483-8. PMID 7762591 DOI: 10.1002/Ajmg.1320550418 |
0.441 |
|
| 1995 |
Scott JA, Wenger SL, Steele MW, Chakravarti A. Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation. American Journal of Medical Genetics. 56: 67-71. PMID 7747789 DOI: 10.1002/Ajmg.1320560115 |
0.421 |
|
| 1995 |
Lewis KE, Lubetsky MJ, Wenger SL, Steele MW. Chromosomal abnormalities in a psychiatric population American Journal of Medical Genetics - Neuropsychiatric Genetics. 60: 53-54. PMID 7485235 DOI: 10.1002/ajmg.1320600110 |
0.339 |
|
| 1993 |
Donahue SP, Wenger SL, Steele MW, Gorin MB. Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocation. Ophthalmic Paediatrics and Genetics. 14: 17-21. PMID 8345951 DOI: 10.3109/13816819309087618 |
0.379 |
|
| 1993 |
Kocova M, Siegel SF, Wenger SL, Lee PA, Trucco M. Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA. Lancet (London, England). 342: 140-3. PMID 8101256 DOI: 10.1016/0140-6736(93)91345-M |
0.368 |
|
| 1992 |
Reeser SL, Wenger SL. Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndrome. American Journal of Medical Genetics. 42: 815-9. PMID 1554020 DOI: 10.1002/ajmg.1320420614 |
0.375 |
|
| 1992 |
Becker RA, Surti U, Wenger SL. Sister chromatid exchange and chromosome breakage in complete hydatidiform moles. Cancer Genetics and Cytogenetics. 62: 53-7. PMID 1521235 DOI: 10.1016/0165-4608(92)90039-B |
0.391 |
|
| 1991 |
Yen PH, Tsai SP, Wenger SL, Steele MW, Mohandas TK, Shapiro LJ. X/Y translocations resulting from recombination between homologous sequences on Xp and Yq. Proceedings of the National Academy of Sciences of the United States of America. 88: 8944-8. PMID 1924355 DOI: 10.1073/pnas.88.20.8944 |
0.35 |
|
| 1990 |
Wenger SL. Nonmodal chromosome gain and loss in human fibroblast cultures. Cytogenetics and Cell Genetics. 52: 201. PMID 2698323 DOI: 10.1159/000132879 |
0.325 |
|
| 1990 |
Ritter CL, Steele MW, Wenger SL, Cohen BA. Chromosome mosaicism in hypomelanosis of Ito. American Journal of Medical Genetics. 35: 14-7. PMID 2301465 DOI: 10.1002/ajmg.1320350104 |
0.447 |
|
| 1990 |
Berg SL, Phebus CK, Wenger SL. Juvenile chronic myelogenous leukemia with abnormalities of chromosomes 4 and 5. Cancer Genetics and Cytogenetics. 44: 55-9. PMID 2293880 DOI: 10.1016/0165-4608(90)90197-I |
0.446 |
|
| 1990 |
Yu WD, Wenger SL, Steele MW. X chromosome imprinting in fragile X syndrome. Human Genetics. 85: 590-4. PMID 2227950 DOI: 10.1007/BF00193580 |
0.415 |
|
| 1989 |
Wenger SL, Rauch SD, Hanchett JM. Sister chromatid exchange analysis of the 15q11 region in Prader-Willi syndrome patients. Human Genetics. 83: 111-4. PMID 2777249 DOI: 10.1007/BF00286700 |
0.431 |
|
| 1989 |
Payton JB, Steele MW, Wenger SL, Minshew NJ. The fragile X marker and autism in perspective. Journal of the American Academy of Child and Adolescent Psychiatry. 28: 417-21. PMID 2738009 DOI: 10.1097/00004583-198905000-00019 |
0.322 |
|
| 1988 |
Lin AE, Garver KL, Diggans G, Clemens M, Wenger SL, Steele MW, Jones MC, Israel J. Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes American Journal of Medical Genetics. 31: 533-548. PMID 3067575 DOI: 10.1002/ajmg.1320310308 |
0.394 |
|
| 1988 |
Przylepa KA, Wenger SL. Chromosome breaks and fragile sites in leukemic bone marrow cells. Cancer Genetics and Cytogenetics. 33: 35-8. PMID 2968151 DOI: 10.1016/0165-4608(88)90047-7 |
0.466 |
|
| 1984 |
Wenger SL, Golden WL, Dennis SP, Steele MW. Are the occasional aneuploid cells in peripheral blood cultures significant? American Journal of Medical Genetics. 19: 715-9. PMID 6517096 DOI: 10.1002/ajmg.1320190411 |
0.481 |
|
| 1984 |
Steele MW, Wenger SL, Geweke LO, Golden WL. The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1. Clinical Genetics. 25: 59-62. PMID 6336317 DOI: 10.1111/j.1399-0004.1984.tb00463.x |
0.392 |
|
| 1981 |
Wenger SL, Steele MW. Meiotic consequences of pericentric inversions of chromosome 13. American Journal of Medical Genetics. 9: 275-83. PMID 7294066 DOI: 10.1002/ajmg.1320090403 |
0.371 |
|
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