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Sharon Wenger

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TOP 3
Olukemi A Esan; Jamie R Senft; Sharon L Wenger
Patterns of BCR/ABL Gene Rearrangements in Chronic Myeloid Leukemia with Complex t(9;22) Using Fluorescence In Situ Hybridization (FISH).
Nathanael G Bailey; Marybeth Hummel; Sarah T South; Sharon L Wenger
Case report: cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with wolf-hirschhorn syndrome.
Jasen L Wise; Richard J Crout; Daniel W McNeil; Robert J Weyant; Mary L Marazita; Sharon L Wenger
Human telomere length correlates to the size of the associated chromosome arm.

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All Publications

2012: Olukemi A Esan; Jamie R Senft; Sharon L Wenger
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 2012;38(1):5-7.
2010: Nathanael G Bailey; Marybeth Hummel; Sarah T South; Sharon L Wenger
Case report: cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with wolf-hirschhorn syndrome.
Journal of the Association of Genetic Technologists 2010;36(1):5-10.
2009: Jasen L Wise; Richard J Crout; Daniel W McNeil; Robert J Weyant; Mary L Marazita; Sharon L Wenger
Human telomere length correlates to the size of the associated chromosome arm.
PloS one 2009;4(6):e6013.
2009: Jasen L Wise; Richard J Crout; Daniel W McNeil; Robert J Weyant; Mary L Marazita; Sharon L Wenger
Cryptic subtelomeric rearrangements and X chromosome mosaicism: a study of 565 apparently normal individuals with fluorescent in situ hybridization.
PloS one 2009;4(6):e5855.
2008: Paul H Hartel; Amy L Shackelford; James V Hartel; Sharon L Wenger
Del(5q) is associated with clinical and histological parameters in small cell neuroendocrine lung carcinoma.
International journal of surgical pathology 2008;16(4):419-23.
2007: Timothy Wiltshire; Jamie Senft; Yutian Wang; Gregory W Konat; Sharon L Wenger; Eddie Reed; Weixin Wang
BRCA1 contributes to cell cycle arrest and chemoresistance in response to the anticancer agent irofulven.
Molecular pharmacology 2007;71(4):1051-60.
2006: Yutian Wang; Timothy Wiltshire; Jamie Senft; Sharon L Wenger; Eddie Reed; Weixin Wang
Fanconi anemia D2 protein confers chemoresistance in response to the anticancer agent, irofulven.
Molecular cancer therapeutics 2006;5(12):3153-61.
2006: Sharon L Wenger; Paul D Grossfeld; Benjamin L Siu; James E Coad; Frank G Keller; Marybeth Hummel
Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome.
American journal of medical genetics. Part A 2006;140(7):704-8.
2006: Jason Bennett; Angela C Obringer; H James Williams; Sharon L Wenger
Cytogenetic analysis in various tissues of pregnancy loss.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(2):136.
2006: Seth M Weinberg; Katherine Neiswanger; Rick A Martin; Mark P Mooney; Alex A Kane; Sharon L Wenger; Joseph E Losee; Frederic W-B Deleyiannis; Lian Ma; Javier Enríquez De Salamanca; Andrew E Czeizel; Mary L Marazita
The Pittsburgh Oral-Facial Cleft study: expanding the cleft phenotype. Background and justification.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2006;43(1):7-20.
2005: Min Yu; Angela C Obringer; Melissa H Fowler; Marybeth Hummel; Sharon L Wenger
Prenatal detection of deletion 6q13q15 in a complex karyotype.
Prenatal diagnosis 2005;25(12):1084-7.
2005: Viktoria N Evdokimova; Reagan K McLoughlin; Sharon L Wenger; Stephen G Grant
Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.
American journal of medical genetics. Part A 2005;135(1):59-65.
2005: Wozhan Tang; Sharon L Wenger
Cell death as a possible mechanism for tissue limited mosaicism in Pallister-Killian syndrome.
Journal of the Association of Genetic Technologists 2005;31(4):168-9.
2005: Dana M Wonsettler; William W L Chang; Sharon L Wenger
Extra copy of 20q deletion, acute myelomonocytic leukemia (M4) and Niemann-Pick disease.
Journal of the Association of Genetic Technologists 2005;31(2):55-8.
2004: Sharon L Wenger; Jamie Senft; Linda M Sargent; R N K Bamezai; Narendra K Bairwa; Stephen G Grant
Comparison of established cell lines at different passages by karyotype and comparative genomic hybridization.
Bioscience reports 2004;24(6):631-9.
2004: Darren L Harris; Benjamin L Siu; Marybeth Hummel; Kerry Harbert; Jamie Senft; Linda M Sargent; Sharon L Wenger
Mosaic ring 12p and total anomalous pulmonary venous return.
American journal of medical genetics. Part A 2004;131(1):91-3.
2004: Sharon L Wenger; Ona C Bleigh; Marybeth Hummel
Cleft palate in a newborn with duplication 2(q13q23).
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2004;41(5):568-70.
2004: Vera A Voronina; Elena A Kozhemyakina; Christina M O'Kernick; Natan D Kahn; Sharon L Wenger; John V Linberg; Adele S Schneider; Peter H Mathers
Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea.
Human molecular genetics 2004;13(3):315-22.
2003: Jason C Fowler; Peter F Ehrlich; Sharon L Wenger; Barbara S Ducatman
Pathologic quiz case: a 10-year-old girl with a pelvic mass.
Archives of pathology & laboratory medicine 2003;127(5):633-5.
2002: Sobha Kurian; Thomas F Hogan; Ona C Bleigh; Yvonne G Dowdy; Taha Merghoub; Pier Paolo Pandolfi; Sharon L Wenger
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 2002;138(2):143-8.
2002: Sallie L McAdoo; Ona C Bleigh; G Millard Simmons; Sharon L Wenger
Maternal cell contamination in an amniotic fluid sample.
Prenatal diagnosis 2002;22(8):737.
2001: Sharon L Wenger; C Cutenese; M Hummel
Three-way unbalanced translocation in a mildly dysmorphic mentally retarded child.
Clinical genetics 2001;59(2):139-40.
2000: Stephen G Grant; Sharon L Wenger; Jean J Latimer; D Thull; L W Burke
Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome.
Clinical genetics 2000;58(3):209-15.
2000: B V Ndah; J A Stead; L R Brancazio; M Hummel; Sharon L Wenger
Prenatal detection of trisomy for the entire long arm of chromosome 7.
Journal of medical genetics 2000;37(7):551-3.
2000: Sharon L Wenger; L Y Boone; J H Cummins; M A Del Vecchio; C A Bay; Marybeth Hummel; P A Mowery-Rushton
Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.
American journal of medical genetics 2000;91(5):351-4.
2000: C Cutenese; M Mullett; M Hummel; Sharon L Wenger
Ring chromosome 1 in a newborn.
Clinical dysmorphology 2000;9(2):131-3.
1999: Sharon L Wenger; C Cutenese; L R Brancazio
Detection of pericentric inversion of X chromosome in a male fetus.
American journal of medical genetics 1999;87(4):339-41.
1998: Peter K Rogan; JR Seip; LM White; Sharon L Wenger; MW Steele; M A Sperling; Ramkumar Menon; Joan H M Knoll
Relaxation of imprinting in Prader-Willi syndrome.
Human genetics 1998;103(6):694-701.
1997: Sharon L Wenger; E W McPherson
Interstitial deletion 2(p11.2p13): a rare chromosomal abnormality.
Clinical genetics 1997;52(1):61-2.
1997: Sharon L Wenger; S L Sell; M J Painter; MW Steele
Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes.
American journal of medical genetics 1997;70(2):150-4.
1997: Sharon L Wenger; L Y Boone; U Surti; MW Steele
Terminal 2q deletion--a recognizable syndrome.
Clinical genetics 1997;51(4):290.
1997: Wendy S Rubinstein; Sharon L Wenger; R M Hoffman; A D Auerbach; JJ Mulvihill
Interstitial lung disease in an adult with Fanconi anemia: clues to the pathogenesis.
American journal of medical genetics 1997;69(3):315-9.
1997: Stephen G Grant; W Reeger; Sharon L Wenger
Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay.
Genetic testing 1997;1(4):261-7.
1996: Sharon L Wenger; C A Giangreco; J Tarleton; H B Wessel
Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.
American journal of medical genetics 1996;66(1):60-3.
1996: C A Giangreco; M W Steele; C E Aston; J H Cummins; Sharon L Wenger
A simplified six-item checklist for screening for fragile X syndrome in the pediatric population.
The Journal of pediatrics 1996;129(4):611-4.
1996: John M Greally; K Neiswanger; J H Cummins; L Y Boone; S G Lenkey; Sharon L Wenger; J L Lewis; D Fischer; R A Paul; M W Steele
A molecular anatomical analysis of mosaic trisomy 16.
Human genetics 1996;98(1):86-90.
1995: Sharon L Wenger
Chemical induction of sister chromatid exchange at fragile sites.
Cancer genetics and cytogenetics 1995;85(1):72-4.
1995: Sharon L Wenger; J H Cummins
Fluorescent in situ hybridization for evaluation of Prader-Willi and Angelman syndromes.
American journal of medical genetics 1995;57(4):639.
1995: J A Scott; Sharon L Wenger; M W Steele; Aravinda Chakravarti
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
American journal of medical genetics 1995;56(1):67-71.
1995: K E Lewis; M J Lubetsky; Sharon L Wenger; M W Steele
Chromosomal abnormalities in a psychiatric population.
American journal of medical genetics 1995;60(1):53-4.
1995: M Kocova; S F Siegel; Sharon L Wenger; Peter A Lee; M Nalesnik; Massimo Trucco
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 1995;55(4):483-8.
1995: Sharon L Wenger; M W Steele; L Y Boone; S G Lenkey; J H Cummins; X Q Chen
"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents.
American journal of medical genetics 1995;55(1):47-52.
1994: Julie Blatt; A Katerji; M Barmada; Sharon L Wenger; L Penchansky
Pancytopenia and vacuolation of marrow precursors associated with necrotizing encephalopathy.
British journal of haematology 1994;86(1):207-9.
1994: Sharon L Wenger; Urvashi Surti; N A Nwokoro; M W Steele
Cytogenetic characterization of cat eye syndrome marker chromosome.
Annales de génétique 1994;37(1):33-6.
1993: M Kocova; S F Siegel; Sharon L Wenger; Peter A Lee; Massimo Trucco
Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA.
Lancet 1993;342(8864):140-3.
1992: John M Greally; L Y Boone; S G Lenkey; Sharon L Wenger; M W Steele
Acrometageria: a spectrum of "premature aging" syndromes.
American journal of medical genetics 1992;44(3):334-9.
1992: R A Becker; Urvashi Surti; Sharon L Wenger
Sister chromatid exchange and chromosome breakage in complete hydatidiform moles.
Cancer genetics and cytogenetics 1992;62(1):53-7.
1992: Sharon L Wenger; M W Steele; Eric Hoffman; M A Barmada; H B Wessel
X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers.
American journal of medical genetics 1992;43(6):1012-5.
1992: S L Reeser; Sharon L Wenger
Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndrome.
American journal of medical genetics 1992;42(6):815-9.
1991: C A Munn; Sharon L Wenger; M W Steele
Assessment of X bends in patients with atypical X chromosome phenotypes.
Annales de génétique 1991;34(2):120-4.
1990: Wei-Dong Yu; Sharon L Wenger; M W Steele
X chromosome imprinting in fragile X syndrome.
Human genetics 1990;85(6):590-4.
1990: Sharon L Wenger; L Y Boone; M W Steele
Mosaicism in Pallister i(12p) syndrome.
American journal of medical genetics 1990;35(4):523-5.
1990: C L Ritter; M W Steele; Sharon L Wenger; B A Cohen
Chromosome mosaicism in hypomelanosis of Ito.
American journal of medical genetics 1990;35(1):14-7.
1990: S L Berg; C K Phebus; Sharon L Wenger
Juvenile chronic myelogenous leukemia with abnormalities of chromosomes 4 and 5.
Cancer genetics and cytogenetics 1990;44(1):55-9.
1989: Sharon L Wenger; S D Rauch; J M Hanchett
Sister chromatid exchange analysis of the 15q11 region in Prader-Willi syndrome patients.
Human genetics 1989;83(2):111-4.
1988: Sharon L Wenger; M W Steele; Wei-Dong Yu
Risk effect of maternal age in Pallister i(12p) syndrome.
Clinical genetics 1988;34(3):181-4.
1988: K A Przylepa; Sharon L Wenger
Chromosome breaks and fragile sites in leukemic bone marrow cells.
Cancer genetics and cytogenetics 1988;33(1):35-8.
1988: Sharon L Wenger; Julie Blatt; M W Steele; D A Lloyd; M Bellinger; C K Phebus; M Horn; R Jaffe
Rhabdomyosarcoma in Roberts syndrome.
Cancer genetics and cytogenetics 1988;31(2):285-9.
1987: Sharon L Wenger; J M Hanchett; M W Steele; B V Maier; W L Golden
Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion.
American journal of medical genetics 1987;28(4):881-7.