Schrager, JJ, Vnencak-Jones, CL, Graber, SE, Neff, AT, Chari, RS, Wright, KJ, Pinson, CW, Stewart, JH, Gorden, DL. Use of short tandem repeats for DNA fingerprinting to rapidly diagnose graft-versus-host
disease in solid organ transplant patients. Transplantation, 81(1), 21-5, 2006
Pitchford, CW, Creech, CB, Peters, TR, Vnencak-Jones, CL. Bartonella henselae Endocarditis in a Child. Pediatr Cardiol, 27(6), 769-71, 2006
Woods-Swafford, W, Vnencak-Jones, CL, Loken, MR, Manes, B, Frangoul, H. Mobilization of Ph chromosome-negative peripheral blood stem cells in a child
with chronic myeloid leukemia after imatinib-induced complete molecular remission. Pediatr Blood Cancer, 2006
Bregman, SG, Yeaney, GA, Greig, BW, Vnencak-Jones, CL, Hamilton, KS. Subcutaneous panniculitic T-cell lymphoma in a cardiac allograft recipient. J Cutan Pathol, 32(5), 366-70, 2005
Fossey, SC, Ferreira-Gonzalez, A, Garrett, CT, Dumur, CI, Vnencak-Jones, CL. BCRABL transcript detection by quantitative real-time PCR : are correlated
results possible from homebrew assays. Mol Diagn, 9(4), 187-93, 2005
Cogan, JD, Vnencak-Jones, CL, Phillips, JA, Lane, KB, Wheeler, LA, Robbins, IM, Garrison, G, Hedges, LK, Loyd, JE. Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary
hypertension. Genet Med, 7(3), 169-74, 2005
Garland, EM, Vnencak-Jones, CL, Biaggioni, I, Davis, TL, Montine, TJ, Robertson, D. Fragile X gene premutation in multiple system atrophy. J Neurol Sci, 227(1), 115-8, 2004
Zhuang, Z, Lee, YS, Zeng, W, Furuta, M, Valyi-Nagy, T, Johnson, MD, Vnencak-Jones, CL, Woltjer, RL, Weil, RJ. Molecular genetic and proteomic analysis of synchronous malignant gliomas. Neurology, 62(12), 2316-9, 2004
Juskevicius, R, Vnencak-Jones, C. Pathologic quiz case: a 17-year-old renal transplant patient with persistent
fever, pancytopenia, and axillary lymphadenopathy. Bacillary angiomatosis of the lymph node in the renal
transplant recipient. Arch Pathol Lab Med, 128(1), e12-4, 2004
Johnson, MD, Vnencak-Jones, CL, Toms, SA, Moots, PM, Weil, R. Allelic losses in oligodendroglial and oligodendroglioma-like neoplasms: analysis
using microsatellite repeats and polymerase chain reaction. Arch Pathol Lab Med, 127(12), 1573-9, 2003
Boyd, AS, Vnencak-Jones, CL. T-cell clonality in lichenoid purpura: a clinical and molecular evaluation
of seven patients. Histopathology, 43(3), 302-3, 2003
Runo, James R, Vnencak-Jones, Cindy L, Prince, Melissa, Loyd, James E, Wheeler, Lisa, Robbins, Ivan M, Lane, Kirk B, Newman, John H, Johnson, Joyce, Nichols, William C, Phillips, John A. Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II.. Am J Respir Crit Care Med, 167(6), 889-94, 2003
Lane, Joshua E, Ribeiro-Rodrigues, Rodrigo, Olivares-Villag??mez, Danyvid, Vnencak-Jones, Cindy L, McCurley, Thomas L, Carter, Clint E. Detection of Trypanosoma cruzi DNA within murine cardiac tissue sections by in situ polymerase chain reaction.. Mem Inst Oswaldo Cruz, 98(3), 373-6, 2003
Vnencak-Jones, Cindy L. Fluorescence PCR and GeneScan analysis for the detection of CAG repeat expansions associated with Huntington's disease.. Methods Mol Biol, 217, 101-8, 2003
Smith, David I, Vnencak-Jones, Cindy L, Boyd, Alan S. T-lymphocyte clonality in benign lichenoid keratoses.. J Cutan Pathol, 29(10), 623-4, 2002
Tranebjaerg, L, Jensen, P K, Van Ghelue, M, Vnencak-Jones, C L, Sund, S, Elgjo, K, Jakobsen, J, Lindal, S, Warburg, M, Fuglsang-Frederiksen, A, Skullerud, K. Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene.. Ophthalmic Genet, 22(4), 207-23, 2001
Macon, W R, Levy, N B, Kurtin, P J, Salhany, K E, Elkhalifa, M Y, Casey, T T, Craig, F E, Vnencak-Jones, C L, Gulley, M L, Park, J P, Cousar, J B. Hepatosplenic alphabeta T-cell lymphomas: a report of 14 cases and comparison with hepatosplenic gammadelta T-cell lymphomas.. Am J Surg Pathol, 25(3), 285-96, 2001
Kasami, M, Gobbi, H, Dupont, WD, Simpson, JF, Page, DL, Vnencak-Jones, CL. Androgen receptor CAG repeat lengths in ductal carcinoma in situ of breast,
longest in apocrine variety. Breast, 9(1), 23-7, 2000
Raskin, S, Phillips, J A, Kaplan, G, McClure, M, Vnencak-Jones, C, Rozov, T, Cardieri, J M, Marostica, P, Abreu, F, Giugliani, R, Reis, F, Rosario, N A, Ludwig, N, Pereira, L, Faucz, F, Gabardo, J, Culpi, L. Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil.. Hum Biol, 71(1), 111-21, 1999
Hodges, K B, Vnencak-Jones, C L, Larson, R S, Kinney, M C. Rarity of genomic instability in pathogenesis of systemic anaplastic large cell lymphoma (ALCL) in immunocompetent patients.. Hum Pathol, 30(2), 173-7, 1999
Miranda, R N, Cousar, J B, Hammer, R D, Collins, R D, Vnencak-Jones, C L. Somatic mutation analysis of IgH variable regions reveals that tumor cells of most parafollicular (monocytoid) B-cell lymphoma, splenic marginal zone B-cell lymphoma, and some hairy cell leukemia are composed of memory B lymphocytes.. Hum Pathol, 30(3), 306-12, 1999
Vnencak-Jones, C L. Molecular testing for inherited diseases.. Am J Clin Pathol, 112(1 Suppl 1), S19-32, 1999
Seeler, R A, Vnencak-Jones, C L, Bassett, L M, Gilbert, J B, Michaelis, R C. Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.. Haemophilia, 5(6), 445-9, 1999
Serpi, M., Hoffmann, G.F., Kircheisen, R., Vnencak-Jones, C., Feist, D., Wermuth, B., Zilow, E., Springer, W., Tonshoff, B., and Dominick, H.C. "Disturbance of Intestinal Transport. Unusual Presenting Symptom in a Neonate with Carbamylphosphate Synthetase Deficiency." . Pediat. Prax., 56, 375-383, 1999
Johnson, M D, Vnencak-Jones, C L, McLean, M J. Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothers.. Neurology, 51(6), 1715-7, 1998
Hammer, R D, Vnencak-Jones, C L, Manning, S S, Glick, A D, Kinney, M C. Microvillous lymphomas are B-cell neoplasms that frequently express CD56.. Mod Pathol, 11(3), 239-46, 1998
Olivares-Villag??mez, D, McCurley, T L, Vnencak-Jones, C L, Correa-Oliveira, R, Colley, D G, Carter, C E. Polymerase chain reaction amplification of three different Trypanosoma cruzi DNA sequences from human chagasic cardiac tissue.. Am J Trop Med Hyg, 59(4), 563-70, 1998
Chapman, J, Cerven?!kov?!, L, Petersen, R B, Lee, H S, Estupinan, J, Richardson, S, Vnencak-Jones, C L, Gajdusek, D C, Korczyn, A D, Brown, P, Goldfarb, L G. APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies.. Neurology, 51(2), 548-53, 1998
Essary, L R, Vnencak-Jones, C L, Manning, S S, Olson, S J, Johnson, J E. Frequency of parvovirus B19 infection in nonimmune hydrops fetalis and utility of three diagnostic methods.. Hum Pathol, 29(7), 696-701, 1998
Stevenson, R E, Arena, J F, Ouzts, E, Gibson, A, Shokeir, M H, Vnencak-Jones, C, Lubs, H A, May, M, Schwartz, C E. Renpenning syndrome maps to Xp11.. Am J Hum Genet, 62(5), 1092-101, 1998
Lamps, L W, Bronner, M P, Vnencak-Jones, C L, Tham, K T, Mertz, H R, Scott, M A. Optimal screening and diagnosis of microsporida in tissue sections: a comparison of polarization, special stains, and molecular techniques.. Am J Clin Pathol, 109(4), 404-10, 1998
Kasami, M, Vnencak-Jones, C L, Manning, S, Dupont, W D, Jensen, R A, Page, D L. Monoclonality in fibroadenomas with complex histology and phyllodal features.. Breast Cancer Res Treat, 50(2), 185-91, 1998
Larson, R S, Manning, S, Macon, W R, Vnencak-Jones, C. Microsatellite instability in natural killer cell-like T-cell lymphomas in immunocompromised and immunocompetent individuals.. Blood, 89(3), 1114-5, 1997
Nance, M.A. and the US Huntington's Disease Genetic Testing Group. "Genetic Testing of Children at Risk for Huntington?s Disease.. Neurology, 49, 1048-1053, 1997
Chen, S G, Parchi, P, Brown, P, Capellari, S, Zou, W, Cochran, E J, Vnencak-Jones, C L, Julien, J, Vital, C, Mikol, J, Lugaresi, E, Autilio-Gambetti, L, Gambetti, P. Allelic origin of the abnormal prion protein isoform in familial prion diseases.. Nat Med, 3(9), 1009-15, 1997
Raskin, S, Phillips, J A, Krishnamani, M R, Vnencak-Jones, C, Parker, R A, Rozov, T, Cardieri, J M, Marostica, P, Abreu, F, Giugliani, R, Reis, F, Rosario, N A, Ludwig, N, Culpi, L. Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution.. Hum Biol, 69(4), 499-508, 1997
Raskin, S, Philips, J A, Krishnamani, M R, Vnencak-Jones, C, Parker, R A, Dawson, E, Rozov, T, Cardieri, J M, Marostica, P, Abreu, F, Giugliani, R, Reis, F, Rosario, N A, Ludwig, N, Culpi, L. Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study.. Hum Biol, 69(1), 75-88, 1997
Kasami, M, Vnencak-Jones, C L, Manning, S, Dupont, W D, Page, D L. Loss of heterozygosity and microsatellite instability in breast hyperplasia. No obligate correlation of these genetic alterations with subsequent malignancy.. Am J Pathol, 150(6), 1925-32, 1997
Lane, J E, Olivares-Villagomez, D, Vnencak-Jones, C L, McCurley, T L, Carter, C E. Detection of Trypanosoma cruzi with the polymerase chain reaction and in situ hybridization in infected murine cardiac tissue.. Am J Trop Med Hyg, 56(6), 588-95, 1997
Hammer, R D, Cousar, J B, Collins, R D, Vnencak-Jones, C L. bc1-1 gene rearrangements in paraffin-embedded tissues.. Am J Clin Pathol, 105(6), 806-7, 1996
Kolquist, K A, Vnencak-Jones, C L, Swift, L, Page, D L, Johnson, J E, Denison, M R. Fatal fat embolism syndrome in a child with undiagnosed hemoglobin S/beta+ thalassemia: a complication of acute parvovirus B19 infection.. Pediatr Pathol Lab Med, 16(1), 71-82, 1996
Larson, R S, Scott, M A, McCurley, T L, Vnencak-Jones, C L. Microsatellite analysis of posttransplant lymphoproliferative disorders: determination of donor/recipient origin and identification of putative lymphomagenic mechanism.. Cancer Res, 56(19), 4378-81, 1996
Scott, M A, McCurley, T L, Vnencak-Jones, C L, Hager, C, McCoy, J A, Anderson, B, Collins, R D, Edwards, K M. Cat scratch disease: detection of Bartonella henselae DNA in archival biopsies from patients with clinically, serologically, and histologically defined disease.. Am J Pathol, 149(6), 2161-7, 1996
Butler, M G, Pratesi, R, Vnencak-Jones, C L. Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.. J Intellect Disabil Res, 39 ( Pt 6), 544-53, 1995
Summar, M L, Dasouki, M J, Schofield, P J, Krishnamani, M R, Vnencak-Jones, C, Tuchman, M, Mao, J, Phillips, J A. Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35.. Cytogenet Cell Genet, 71(3), 266-7, 1995
Parchi, P, Castellani, R, Cortelli, P, Montagna, P, Chen, S G, Petersen, R B, Manetto, V, Vnencak-Jones, C L, McLean, M J, Sheller, J R. Regional distribution of protease-resistant prion protein in fatal familial insomnia.. Ann Neurol, 38(1), 21-9, 1995
Antonarakis, SE, Rossiter, JP, Young, M, Horst, J, de Moerloose, P, Sommer, SS, Ketterling, RP, Kazazian, HH, N??grier, C, Vinciguerra, C, Gitschier, J, Goossens, M, Girodon, E, Ghanem, N, Plassa, F, Lavergne, JM, Vidaud, M, Costa, JM, Laurian, Y, Lin, SW, Lin, SR, Shen, MC, Lillicrap, D, Taylor, SA, Windsor, S, Valleix, SV, Nafa, K, Sultan, Y, Delpech, M, Vnencak-Jones, CL, Phillips, JA, Ljung, RC, Koumbarelis, E, Gialeraki, A, Mandalaki, T, Jenkins, PV, Collins, PW, Pasi, KJ, Goodeve, A, Peake, I, Preston, FE, Schwartz, M, Scheibel, E, Ingerslev, J, Cooper, DN, Millar, DS, Kakkar, VV, Giannelli, F, Naylor, JA, Tizzano, EF, Baiget, M, Domenech, M, Altisent, C, Tusell, J, Beneyto, M, Lorenzo, JI, Gaucher, C, Mazurier, C, Peerlinck, K, Matthijs, G, Cassiman, JJ, Vermylen, J, Mori, PG, Acquila, M, Caprino, D, Inaba, H. Factor VIII gene inversions in severe hemophilia A: results of an international
consortium study. Blood, 86(6), 2206-12, 1995
Butler, M G, Pratesi, R, Vnencak-Jones, C L. Molecular genetic screening in cytogenetically normal mentally retarded males with manifestations of fragile X syndrome.. Am J Med Genet, 51(4), 315-6, 1994
Sukpanichnant, S, Vnencak-Jones, C L, McCurley, T L. Determination of B-cell clonality in paraffin-embedded endoscopic biopsy specimens of abnormal lymphocytic infiltrates and gastrointestinal lymphoma by polymerase chain reaction.. Am J Clin Pathol, 102(3), 299-305, 1994
Caleffi, M, Teague, M W, Jensen, R A, Vnencak-Jones, C L, Dupont, W D, Parl, F F. p53 gene mutations and steroid receptor status in breast cancer. Clinicopathologic correlations and prognostic assessment.. Cancer, 73(8), 2147-56, 1994
Dahir, G A, Vnencak-Jones, C L, Schwartz, H S, Butler, M G. Dosage and allelic restriction fragment studies and PCR analysis of the H-ras locus in giant cell tumor of bone.. Cancer Genet Cytogenet, 74(2), 95-8, 1994
O'Malley, F P, Vnencak-Jones, C L, Dupont, W D, Parl, F, Manning, S, Page, D L. p53 mutations are confined to the comedo type ductal carcinoma in situ of the breast. Immunohistochemical and sequencing data.. Lab Invest, 71(1), 67-72, 1994
Dupont, W D, Page, D L, Parl, F F, Vnencak-Jones, C L, Plummer, W D, Rados, M S, Schuyler, P A. Long-term risk of breast cancer in women with fibroadenoma.. N Engl J Med, 331(1), 10-5, 1994
Ulm, Janet E, Vnencak-Jones, Cindy L, Bosque, Patrick. Research on familial Creutzfeldt-Jakob disease (FCJD) resulting in presymptomatic testing: implications for the Human Genome Project.. J Genet Couns, 2(1), 9-15, 1993
Jones, E M, Colley, D G, Tostes, S, Lopes, E R, Vnencak-Jones, C L, McCurley, T L. Amplification of a Trypanosoma cruzi DNA sequence from inflammatory lesions in human chagasic cardiomyopathy.. Am J Trop Med Hyg, 48(3), 348-57, 1993
Raskin, S, Phillips, J A, Krishnamani, M R, Vnencak-Jones, C, Parker, R A, Rozov, T, Cardieri, J M, Marostica, P, Abreu, F, Giugliani, R. DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards.. Am J Med Genet, 46(6), 665-9, 1993
Sukpanichnant, S, Vnencak-Jones, C L, McCurley, T L. Detection of clonal immunoglobulin heavy chain gene rearrangements by polymerase chain reaction in scrapings from archival hematoxylin and eosin-stained histologic sections: implications for molecular genetic studies of focal pathologic lesions.. Diagn Mol Pathol, 2(3), 168-76, 1993
Tuchman, M, Mauer, S M, Holzknecht, R A, Summar, M L, Vnencak-Jones, C L. Prospective versus clinical diagnosis and therapy of acute neonatal hyperammonaemia in two sisters with carbamyl phosphate synthetase deficiency.. J Inherit Metab Dis, 15(2), 269-77, 1992
Jones, E M, Colley, D G, Tostes, S, Lopes, E R, Vnencak-Jones, C L, McCurley, T L. A Trypanosoma cruzi DNA sequence amplified from inflammatory lesions in human chagasic cardiomyopathy.. Trans Assoc Am Physicians, 105, 182-9, 1992
Raskin, S, Phillips, J A, Vnencak-Jones, C, Dawson, E, Kaplan, G, McClure, M. Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysis.. Biotechniques, 13(3), 372-4, 1992
Tharapel, S A, Vnencak-Jones, C L, Whitlock, J A, Jain, R. Molecular confirmation of BCR-ABL fusion in a chronic myeloid leukemia with a complex translocation involving chromosomes 9, 15, and 22.. Genes Chromosomes Cancer, 4(4), 343-5, 1992
Vnencak-Jones, C L, Phillips, J A. Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH). Am J Hum Genet, 50(4), 871-2, 1992
Bosque, P J, Vnencak-Jones, C L, Johnson, M D, Whitlock, J A, McLean, M J. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease.. Neurology, 42(10), 1864-70, 1992
Raskin, S, Phillips, J A, Kaplan, G, McClure, M, Vnencak-Jones, C. Cystic fibrosis genotyping by direct PCR analysis of Guthrie blood spots.. PCR Methods Appl, 2(2), 154-6, 1992
Vnencak-Jones, C L, Phillips, J A, Wang, D F. Use of polymerase chain reaction in detection of growth hormone gene deletions.. J Clin Endocrinol Metab, 70(6), 1550-3, 1990
Vnencak-Jones, C L, Phillips, J A. Hot spots for growth hormone gene deletions in homologous regions outside of Alu repeats.. Science, 250(4988), 1745-8, 1990
Phillips, J A, Vnencak-Jones, C L. Genetics of growth hormone and its disorders.. Adv Hum Genet, 18, 305-63, 1989
Vnencak-Jones, C L, Phillips, J A, Chen, E Y, Seeburg, P H. Molecular basis of human growth hormone gene deletions.. Proc Natl Acad Sci U S A, 85(15), 5615-9, 1988
Vnencak-Jones, C L, Wahab, S Z, Zehner, Z E, Holmes, W M. A human tRNA(iMet) gene produces multiple transcripts.. Mol Cell Biol, 7(11), 4134-8, 1987
