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S. Wenger · SciRah

Researcher profile · Semantic Scholar

S. Wenger

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S. Wenger — researcher profile on SciRah

h-index: 19
Works: 72
Citations: 1,741

Most-cited papers

The spectrum of WRN mutations in Werner syndrome patients
Shurong Huang, Lin Lee, N. Hanson, C. Lenaerts +30 more
2006Human Mutation224 citations Open access
Semantic Scholar
Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea.
V. Voronina, E. Kozhemyakina, Christina M. O'Kernick, NA Kahn +4 more
2003Human Molecular Genetics217 citations Open access
Semantic Scholar
Comparison of Established Cell Lines at Different Passages by Karyotype and Comparative Genomic Hybridization
S. Wenger, J. Senft, L. Sargent, R. Bamezai +2 more
2004Bioscience Reports133 citations
Semantic Scholar
The Pittsburgh Oral-Facial Cleft Study: Expanding the Cleft Phenotype. Background and Justification
S. Weinberg, K. Neiswanger, Rick A. Martin, M. Mooney +8 more
2006The Cleft Palate-Craniofacial Journal112 citations
Semantic Scholar
Chromosome mosaicism in hypomelanosis of Ito.
C. Ritter, Mark W. Steele, S. Wenger, B. Cohen
1990American journal of medical genetics110 citations
Semantic Scholar
Molecular and phenotypic characterization of ring chromosome 22
A. Jeffries, S. Curran, F. Elmslie, Ajay Sharma +3 more
2005American Journal of Medical Genetics. Part A101 citations
Semantic Scholar
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
Jennifer A. Scott, S. Wenger, M. Steele, A. Chakravarti
1995American journal of medical genetics73 citations Open access
Semantic Scholar
X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.
P. Yen, S.-P. Tsai, S. Wenger, M. Steele +2 more
1991Proceedings of the National Academy of Sciences of the United States of America71 citations Open access
Semantic Scholar
Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA.
M. Kocova, S. F. Siegel, M. Trucco, P. A. Lee +1 more
1993The Lancet69 citations
Semantic Scholar
A simplified six-item checklist for screening for fragile X syndrome in the pediatric population.
Cheryl A. Giangreco, M. Steele, C. Aston, J. H. Cummins +1 more
1996Jornal de Pediatria62 citations
Semantic Scholar
Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocation.
S. Donahue, S. Wenger, M. Steele, M. Gorin
1993Ophthalmic Paediatrics and Genetics59 citations Open access
Semantic Scholar
Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits.
M. Mooney, C. Aston, M. Siegel, H. Losken +6 more
1996Journal of Craniofacial Genetics and Developmental Biology55 citations
Semantic Scholar
BRCA1 Contributes to Cell Cycle Arrest and Chemoresistance in Response to the Anticancer Agent Irofulven
T. Wiltshire, J. Senft, Yu-Tian Wang, G. Konat +3 more
2007Molecular Pharmacology36 citations
Semantic Scholar
Tissue Culture of Human Renal Epithelial Cells Using a Defined Serum-Free Growth Formulation
D. Sens, C. Detrisac, M. Sens, Mike R. Rossi +2 more
1999Nephron Experimental Nephrology36 citations
Semantic Scholar
Chromosomal mapping of the human M6 genes.
S. Olinsky, B. Loop, A. Dekosky, Benedetta Ripepi +6 more
1996Genomics33 citations
Semantic Scholar
Human Telomere Length Correlates to the Size of the Associated Chromosome Arm
J. Wise, R. Crout, D. McNeil, R. Weyant +2 more
2009PLoS ONE27 citations Open access
Semantic Scholar
Analysis of genomic instability using multiple assays in a patient with Rothmund–Thomson syndrome
S. G. Grant, S. Wenger, J. Latimer, D. Thull +1 more
2000Clinical Genetics25 citations Open access
Semantic Scholar
Clinical consequences ofdeletion lp35
S. Wenger, M. Steele
198721 citations
Semantic Scholar
Acrometageria: a spectrum of "premature aging" syndromes.
J. Greally, L. Y. Boone, S. G. Lenkey, S. Wenger +1 more
1992American journal of medical genetics20 citations
Semantic Scholar
The cytogenetic, proliferative and viability effects of four bacteriophages on human lymphocytes
S. Wenger, J. Turner, J. Petricciani
1978In Vitro19 citations
Semantic Scholar
Case of Pallister-Killian syndrome with imperforate anus.
A. Lin, M. Clemens, K. Garver, S. Wenger +3 more
1988American journal of medical genetics18 citations
Semantic Scholar
Fanconi anemia D2 protein confers chemoresistance in response to the anticancer agent, irofulven
Yu-Tian Wang, T. Wiltshire, J. Senft, S. Wenger +2 more
2006Molecular Cancer Therapeutics16 citations Open access
Semantic Scholar
Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype
V. N. Evdokimova, Reagan K. McLoughlin, S. Wenger, S. G. Grant
2005American Journal of Medical Genetics. Part A16 citations Open access
Semantic Scholar
Trisomy 8 mosaicism: Selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cells
Bonnie J. Hulley, Marybeth Hummel, L. Cook, Brita K. Boyd +1 more
2003American Journal of Medical Genetics. Part A16 citations
Semantic Scholar
A molecular anatomical analysis of mosaic trisomy 16
John M. Greally, K. Neiswanger, J. H. Cummins, L. Y. Boone +6 more
1996Human Genetics13 citations
Semantic Scholar
Cell death as a possible mechanism for tissue limited mosaicism in Pallister-Killian syndrome.
Wo-Zhan Tang, S. Wenger
2005Journal of the Association of Genetic Technologists12 citations
Semantic Scholar
RepSox Slows Decay of CD34+ Acute Myeloid Leukemia Cells and Decreases T Cell Immunoglobulin Mucin‐3 Expression
Audrey N. Jajosky, J. Coad, J. Vos, Karen H. Martin +3 more
2014Stem Cells Translational Medicine11 citations Open access
Semantic Scholar
Del(5q) Is Associated With Clinical and Histological Parameters in Small Cell Neuroendocrine Lung Carcinoma
P. Hartel, Amy L. Shackelford, J. V. Hartel, S. Wenger
2008International Journal of Surgical Pathology11 citations
Semantic Scholar
Decreased telomere length in metaphase and interphase cells from newborns with trisomy 21.
S. Wenger, J. Hansroth, Amy L. Shackelford
2014Gene9 citations
Semantic Scholar
Prenatal detection of deletion 6q13q15 in a complex karyotype
Min Yu, Angela C. Obringer, Melissa H. Fowler, Marybeth Hummel +1 more
2005Prenatal Diagnosis8 citations
Semantic Scholar
Mosaic ring 12p and total anomalous pulmonary venous return
Darren L. Harris, Benjamin L. Siu, Marybeth Hummel, Kerry A Harbert +3 more
2004American Journal of Medical Genetics. Part A8 citations
Semantic Scholar
X chromosome imprinting in fragile×syndrome
Wei-dong Yu, S. Wenger, M. Steele
1990Human Genetics8 citations
Semantic Scholar
Cryptic Subtelomeric Rearrangements and X Chromosome Mosaicism: A Study of 565 Apparently Normal Individuals with Fluorescent In Situ Hybridization
J. Wise, R. Crout, D. McNeil, R. Weyant +2 more
2009PLoS ONE7 citations Open access
Semantic Scholar
Incorporation of bacteriophage DNA into the genome of cultured human lymphocytes
S. Wenger, M. Steele, J. Turner
1981In Vitro7 citations
Semantic Scholar
Case report: cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with wolf-hirschhorn syndrome.
N. Bailey, S. South, Marybeth Hummel, S. Wenger
2010Journal of the Association of Genetic Technologists6 citations
Semantic Scholar
Relationship between fragile sites and cancer breakpoints.
S. Wenger
1992Cancer Genetics and Cytogenetics6 citations
Semantic Scholar
Screening for cryptic chromosomal abnormalities in patients with mental retardation and dysmorphic facial features using telomere fish probes
Bonnie J. Hulley, Marybeth Hummel, S. Wenger
2003American Journal of Medical Genetics. Part A5 citations
Semantic Scholar
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.
S. Kurian, T. Hogan, O. C. Bleigh, Y. Dowdy +3 more
2002Cancer Genetics and Cytogenetics5 citations
Semantic Scholar
Cytogenetic characterization of cat eye syndrome marker chromosome.
S. Wenger, U. Surti, N. Nwokoro, M. Steele
1994Annales de Genetique5 citations
Semantic Scholar
Patterns of BCR/ABL Gene Rearrangements in Chronic Myeloid Leukemia with Complex t(9;22) Using Fluorescence In Situ Hybridization (FISH).
Olukemi A. Esan, J. Senft, S. Wenger
2012Journal of the Association of Genetic Technologists4 citations
Semantic Scholar
Cytogenetic analysis in various tissues of pregnancy loss
Jason Bennett, A. Obringer, H. J. Williams, S. Wenger
2006Genetics in Medicine4 citations Open access
Semantic Scholar
Cleft Palate in a Newborn with Duplication 2(q13q23)
S. Wenger, O. C. Bleigh, Marybeth Hummel
2004The Cleft Palate-Craniofacial Journal4 citations
Semantic Scholar
"Jumping Translocation" Involving 21p in Amniocytes.
Bonnie J. Hulley, O. C. Bleigh, S. McAdoo, Brita K. Boyd +1 more
2003Journal of the Association of Genetic Technologists4 citations
Semantic Scholar
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
A. Estop, V. Bansal, A. Lin, F. Levinson +4 more
1994American journal of medical genetics4 citations
Semantic Scholar
Safety of desipramine.
J. Payton, M. Steele, S. Wenger, N. Minshew
1989Journal of the American Academy of Child and Adolescent Psychiatry4 citations
Semantic Scholar
Bacteriophages, Vaccines, and People: An Assessment of Risk
J. Petricciani, T.-C. Hsu, A. Stock, J. Turner +2 more
1978Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine4 citations
Semantic Scholar
Maternal cell contamination in an amniotic fluid sample
S. McAdoo, Ona C. Bleigh, G. Simmons, S. Wenger
2002Prenatal Diagnosis3 citations
Semantic Scholar
c-MYC Amplification in Acute Myelogenous Leukemia Evolving from Double Minutes (dmins) to Homogeneously Staining Region (hsr).
Farzaneh Sayedian, J. Senft, M. Spruill, S. Wenger +1 more
2014Journal of the Association of Genetic Technologists2 citations
Semantic Scholar
Persistent Mosaicism for 12p Duplication/Triplication Chromosome Structural Abnormality in Peripheral Blood
Amy L. Shackelford, L. Conlin, Marybeth Hummel, N. Spinner +1 more
2013Case Reports in Genetics2 citations Open access
Semantic Scholar
Acquired Robertsonian translocations in leukemia: two more cases.
Daniel B Herring, Kerry A Harbert, S. Wenger, S. Ericson
2005Cancer Genetics and Cytogenetics2 citations
Semantic Scholar

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J. Senft×7
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S. G. Grant×3
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J. H. Cummins×3

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O. C. Bleigh×3

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