| Year |
Citation |
Score |
| 2023 |
Gudipati M, Butler M, Koka R, Baer MR, Ning Y. Fusion Gene-Based Classification of Variant Cytogenetic Rearrangements in Acute Myeloid Leukemia. Genes. 14. PMID 36833323 DOI: 10.3390/genes14020396 |
0.391 |
|
| 2020 |
Ning Y. Significance of distinguishing 3'-IGH deletion from 5'-IGH deletion in multiple myeloma. Genes, Chromosomes & Cancer. PMID 32893387 DOI: 10.1002/Gcc.22894 |
0.402 |
|
| 2018 |
Gallia GL, Zhang M, Ning Y, Haffner MC, Batista D, Binder ZA, Bishop JA, Hann CL, Hruban RH, Ishii M, Klein AP, Reh DD, Rooper LM, Salmasi V, Tamargo RJ, et al. Genomic analysis identifies frequent deletions of Dystrophin in olfactory neuroblastoma. Nature Communications. 9: 5410. PMID 30575736 DOI: 10.1038/S41467-018-07578-Z |
0.321 |
|
| 2017 |
Koka R, Bade NA, Sausville EA, Ning Y, Zou Y. Unique amplification of BCR-ABL1 gene fusion in a case of T-cell acute lymphoblastic leukemia. Molecular Cytogenetics. 10: 39. PMID 29093755 DOI: 10.1186/S13039-017-0340-6 |
0.387 |
|
| 2017 |
Pallavajjala A, Kim D, Li T, Ghiaur G, Jones RJ, Burns KH, Salzberg SL, Ning Y. Genomic characterization of chromosome translocations in patients with T/myeloid mixed-phenotype acute leukemia. Leukemia & Lymphoma. 1-8. PMID 28882084 DOI: 10.1080/10428194.2017.1372577 |
0.489 |
|
| 2017 |
Nguyen D, Haley L, Pallavajjala A, Gojo I, Ning Y. Identification of a novel KMT2A-SEPT14 fusion in acute myeloid leukemia. Leukemia & Lymphoma. 1-3. PMID 28573893 DOI: 10.1080/10428194.2017.1324163 |
0.364 |
|
| 2016 |
Ning Y. A cryptic translocation leading to NUP98-PHF23 fusion in AML. Best Practice & Research. Clinical Haematology. 29: 320-323. PMID 27890253 DOI: 10.1016/J.Beha.2016.10.002 |
0.406 |
|
| 2016 |
Argani P, Reuter VE, Zhang L, Sung YS, Ning Y, Epstein JI, Netto GJ, Antonescu CR. TFEB-amplified Renal Cell Carcinomas: An Aggressive Molecular Subset Demonstrating Variable Melanocytic Marker Expression and Morphologic Heterogeneity. The American Journal of Surgical Pathology. PMID 27565001 DOI: 10.1097/Pas.0000000000000720 |
0.385 |
|
| 2016 |
Morsberger L, Powell K, Ning Y. A marker chromosome in post-transplant bone marrow. Molecular Cytogenetics. 9: 42. PMID 27252781 DOI: 10.1186/S13039-016-0250-Z |
0.428 |
|
| 2016 |
McCurdy SR, Iglehart BS, Batista DA, Gocke CD, Ning Y, Knaus HA, Jackson AM, Leffell MS, Luznik L, Gojo I. Loss of the mismatched human leukocyte antigen haplotype in two acute Myelogenous leukemia relapses after haploidentical bone marrow transplantation with posttransplantation cyclophosphamide. Leukemia. PMID 27211264 DOI: 10.1038/Leu.2016.144 |
0.307 |
|
| 2016 |
Ho H, Skaist AM, Pallavajjala A, Yonescu R, Batista D, Wheelan SJ, Ning Y. NUP98-PHF23 fusion is recurrent in acute myeloid leukemia and shares gene expression signature of leukemic stem cells. Leukemia Research. 45: 1-7. PMID 27060678 DOI: 10.1016/J.Leukres.2016.03.006 |
0.429 |
|
| 2016 |
Gerber JM, Zeidner JF, Morse S, Blackford AL, Perkins B, Yanagisawa B, Zhang H, Morsberger L, Karp J, Ning Y, Gocke CD, Rosner GL, Smith BD, Jones RJ. Association of Acute Myeloid Leukemia's Most Immature Phenotype with Risk Groups and Outcomes. Haematologica. PMID 26819054 DOI: 10.3324/Haematol.2015.135194 |
0.324 |
|
| 2014 |
Gourdin TS, Zou Y, Ning Y, Emadi A, Duong VH, Tidwell ML, Chen C, Rassool FV, Baer MR. High frequency of rare structural chromosome abnormalities at relapse of cytogenetically normal acute myeloid leukemia with FLT3 internal tandem duplication. Cancer Genetics. 207: 467-73. PMID 25441683 DOI: 10.1016/J.Cancergen.2014.09.001 |
0.442 |
|
| 2014 |
Gough SM, Lee F, Yang F, Walker RL, Zhu YJ, Pineda M, Onozawa M, Chung YJ, Bilke S, Wagner EK, Denu JM, Ning Y, Xu B, Wang GG, Meltzer PS, et al. NUP98-PHF23 is a chromatin-modifying oncoprotein that causes a wide array of leukemias sensitive to inhibition of PHD histone reader function. Cancer Discovery. 4: 564-77. PMID 24535671 DOI: 10.1158/2159-8290.Cd-13-0419 |
0.332 |
|
| 2014 |
Bhatnagar B, Duong VH, Gourdin TS, Tidwell ML, Chen C, Ning Y, Emadi A, Sausville EA, Baer MR. Ten-day decitabine as initial therapy for newly diagnosed patients with acute myeloid leukemia unfit for intensive chemotherapy. Leukemia & Lymphoma. 55: 1533-7. PMID 24144313 DOI: 10.3109/10428194.2013.856425 |
0.331 |
|
| 2014 |
Ning Y, Slovak ML, Schultz RA, Gojo I, Baer MR. Cryptic chromosome abnormalities in a patient with mixed phenotype acute leukemia. Leukemia & Lymphoma. 55: 680-2. PMID 23725388 DOI: 10.3109/10428194.2013.809076 |
0.554 |
|
| 2013 |
Ning Y, Foss A, Kimball AS, Neill N, Matz T, Schultz R. Characterization of a case of follicular lymphoma transformed into B-lymphoblastic leukemia. Molecular Cytogenetics. 6: 34. PMID 23985173 DOI: 10.1186/1755-8166-6-34 |
0.453 |
|
| 2013 |
Trikalinos NA, Chen Q, Ning Y, Sausville EA, Baer MR. Unbalanced 11;18 translocation in an acute erythroid leukemia after radioactive iodine therapy. Cancer Genetics. 206: 252-5. PMID 23871646 DOI: 10.1016/J.Cancergen.2013.06.003 |
0.451 |
|
| 2013 |
Xi Y, Li J, Zan L, Wang J, Wang G, Ning Y. Micro-RNA-16 expression in paraffin-embedded specimen correlates with overall survival of T-lymphoblastic lymphoma/leukemia. Human Pathology. 44: 1011-6. PMID 23260326 DOI: 10.1016/J.Humpath.2012.08.023 |
0.357 |
|
| 2013 |
Schultz RA, Tsuchiya K, Furrow A, Slovak ML, McDaniel LD, Wall M, Crawford E, Ning Y, Saleki R, Fang M, Cawich V, Johnson CE, Minier SL, Neill NJ, Morton SA, et al. CGH-based microarray detection of cryptic and novel copy number alterations and balanced translocations in cytogenetically abnormal cases of b-cell all Health. 5: 23-40. DOI: 10.4236/Health.2013.55A004 |
0.413 |
|
| 2013 |
Gourdin TS, Ning Y, Rassool F, Tidwell M, Duong V, Emadi A, Baer MR. Frequency of rare cytogenetic abnormalities at relapse in acute myeloid leukemia (AML) with FLT3 internal tandem duplication (ITD) and normal karyotype at diagnosis: Evidence for genomic instability? Journal of Clinical Oncology. 31: 7049-7049. DOI: 10.1200/Jco.2013.31.15_Suppl.7049 |
0.4 |
|
| 2013 |
Gough SM, Lee F, Walker RL, Yang F, Zhu Y, Pineda M, Onozawa M, Chung YJ, Bilke S, Wagner EK, Denu JM, Ning Y, Meltzer PS, Aplan PD. Leukemia Driven By a NUP98-Phd Domain Fusion Is Highly Sensitive To Disruption Of H3K4me3-Phd Domain Binding By a Small Molecule Inhibitor Blood. 122: 3759-3759. DOI: 10.1182/Blood.V122.21.3759.3759 |
0.353 |
|
| 2013 |
Gough SM, Lee F, Chung YJ, Walker RL, Yang F, Zhu J, Ning Y, Meltzer PS, Aplan PD. Abstract 3851: NUP98-PHF23 (NP23) binds H3K4me3 and causes a wide spectrum of leukemias, including AML, T-ALL, and pre-B1 ALL. Cancer Research. 73: 3851-3851. DOI: 10.1158/1538-7445.Am2013-3851 |
0.368 |
|
| 2012 |
Bierenbaum J, Davidoff AJ, Ning Y, Tidwell ML, Gojo I, Baer MR. Racial differences in presentation, referral and treatment patterns and survival in adult patients with acute myeloid leukemia: a single-institution experience. Leukemia Research. 36: 140-5. PMID 22112974 DOI: 10.1016/J.Leukres.2011.10.018 |
0.333 |
|
| 2012 |
Jiang N, Qi C, Yu L, Ning Y, An G, Qiu L, Chang H. Analysis of chromosome 12p deletion in plasma cell dyscrasias. Leukemia Research. 36: 32-6. PMID 21982640 DOI: 10.1016/J.Leukres.2011.07.030 |
0.388 |
|
| 2012 |
Gourdin TS, Bhatnagar B, Duffy AP, Tidwell M, Ning Y, Sausville EA, Baer MR. Disease response and survival outcomes in acute myeloid leukemia (AML) patients unfit for chemotherapy treated with 10-day decitabine as initial therapy. Journal of Clinical Oncology. 30: 6611-6611. DOI: 10.1200/Jco.2012.30.15_Suppl.6611 |
0.303 |
|
| 2012 |
Bhatnagar B, Zandberg DP, Vannorsdall EJ, Duffy AP, Tidwell ML, Ning Y, Chen Q, Baer MR. Lack of Response of Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML) to Decitabine After Failure of Azacitidine Blood. 120: 3858-3858. DOI: 10.1182/Blood.V120.21.3858.3858 |
0.309 |
|
| 2011 |
Patel SB, Gojo I, Tidwell M, Ning Y, Zhao XF, Sausville EA, Baer MR. Subdural hematomas in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia receiving imatinib mesylate in conjunction with multi-agent chemotherapy. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 29: 6579. PMID 28020160 DOI: 10.1200/Jco.2011.29.15_Suppl.6579 |
0.4 |
|
| 2011 |
Yu L, Slovak ML, Mannoor K, Chen C, Hunger SP, Carroll AJ, Schultz RA, Shaffer LG, Ballif BC, Ning Y. Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia. Leukemia. 25: 1042-6. PMID 21383747 DOI: 10.1038/Leu.2011.33 |
0.485 |
|
| 2011 |
Yu L, Reader JC, Chen C, Zhao XF, Ha JS, Lee C, York T, Gojo I, Baer MR, Ning Y. Activation of a novel palmitoyltransferase ZDHHC14 in acute biphenotypic leukemia and subsets of acute myeloid leukemia. Leukemia. 25: 367-71. PMID 21151021 DOI: 10.1038/Leu.2010.271 |
0.661 |
|
| 2011 |
Gough SM, Lee F, Chung YJ, Walker RL, Yang F, Zhu Y(, Ning Y, Meltzer PS, Aplan P. A NUP98-PHF23 Transgenic Mouse Model Develops AML and T-ALL Blood. 118: 2467-2467. DOI: 10.1182/Blood.V118.21.2467.2467 |
0.42 |
|
| 2010 |
Meekins J, Butler M, Skinner M, Shippy R, Greene C, Ning Y. Microarray analysis of an unbalanced t(4;13) translocation narrows down the trisomy 13 associated polydactyly to a 7 Mb region. American Journal of Medical Genetics. Part A. 152: 2906-7. PMID 20979195 DOI: 10.1002/Ajmg.A.33691 |
0.343 |
|
| 2010 |
Reader JC, Leng Q, Rassool FV, Ning Y. Regulation of differentiation by a PHD domain in the NUP98-PHF23 fusion protein. Leukemia Research. 34: 1094-7. PMID 20219246 DOI: 10.1016/J.Leukres.2010.02.015 |
0.666 |
|
| 2010 |
Bierenbaum JM, Ning Y, Tidwell M, Gojo I, Baer MR. Race and overall survival in acute myeloid leukemia. Journal of Clinical Oncology. 28: 6570-6570. DOI: 10.1200/Jco.2010.28.15_Suppl.6570 |
0.377 |
|
| 2010 |
Slovak ML, Ning Y, Yu L, Hunger S, Carroll AJ, Brown TC, Campbell LJ, Wall M, Crawford E, Fang M, Kolquist K, Saleki R, Shaffer LG, Ballif B, Schultz R. Targeted Microarray Analyses Augment the Clinical Cytogenetic Diagnosis of Acute Lymphoblastic Leukemia (ALL): Submicroscopic Genetic Events Improve Diagnosis, Contribute to Risk Stratification, and Provide Genetic Markers for Minimal Residual Disease (MRD) Testing Blood. 116: 2690-2690. DOI: 10.1182/Blood.V116.21.2690.2690 |
0.42 |
|
| 2010 |
Zandberg DP, Bierenbaum J, Gojo I, Tidwell ML, Ning Y, Zhao XF, Davidoff AJ, Baer MR. Tertiary Center Referral Patterns for Myelodysplastic Syndrome (MDS) Patients Are Suggestive of Age and Race Disparities Blood. 116: 1881-1881. DOI: 10.1182/Blood.V116.21.1881.1881 |
0.352 |
|
| 2010 |
Ning Y, Yu L, Reader J, Chen C, Zhao XF, Ha JS, Lee C, York T, Gojo I, Baer MR. Activation of a Novel Palmitoyltransferase through a t(6;14) Translocation In T/Myeloid Biphenotypic Leukemia and Subsets of Acute Myeloid Leukemia. Blood. 116: 1663-1663. DOI: 10.1182/Blood.V116.21.1663.1663 |
0.736 |
|
| 2009 |
Butler MS, Ning Y. Improved Detection of a Small Marker Chromosome with Repetitive Sequence-Depleted FISH Probe. Journal of the Association of Genetic Technologists. 35: 164-6. PMID 19952390 |
0.32 |
|
| 2009 |
Bierenbaum J, Ning Y, Hoffman A, Gojo I, Baer MR. Black Patients with Acute Myeloid Leukemia (AML) Are Younger and More Commonly Female, but Have a Higher Incidence of Complex Karyotypes When Compared to Whites. Blood. 114: 2649-2649. DOI: 10.1182/Blood.V114.22.2649.2649 |
0.374 |
|
| 2007 |
Chang H, Ning Y, Qi X, Yeung J, Xu W. Chromosome 1p21 deletion is a novel prognostic marker in patients with multiple myeloma. British Journal of Haematology. 139: 51-4. PMID 17854306 DOI: 10.1111/J.1365-2141.2007.06750.X |
0.439 |
|
| 2007 |
Chang H, Qi X, Xu W, Reader JC, Ning Y. Analysis of 6q deletion in Waldenstrom macroglobulinemia. European Journal of Haematology. 79: 244-7. PMID 17655703 DOI: 10.1111/J.1600-0609.2007.00903.X |
0.712 |
|
| 2007 |
Reader JC, Meekins JS, Gojo I, Ning Y. A novel NUP98-PHF23 fusion resulting from a cryptic translocation t(11;17)(p15;p13) in acute myeloid leukemia. Leukemia. 21: 842-4. PMID 17287853 DOI: 10.1038/Sj.Leu.2404579 |
0.679 |
|
| 2006 |
Chang H, Qi X, Trieu Y, Xu W, Reader JC, Ning Y, Reece D. Multiple myeloma patients with CKS1B gene amplification have a shorter progression-free survival post-autologous stem cell transplantation. British Journal of Haematology. 135: 486-91. PMID 16995883 DOI: 10.1111/J.1365-2141.2006.06325.X |
0.702 |
|
| 2006 |
Chang H, Yeung J, Xu W, Ning Y, Patterson B. Significant increase of CKS1B amplification from monoclonal gammopathy of undetermined significance to multiple myeloma and plasma cell leukaemia as demonstrated by interphase fluorescence in situ hybridisation. British Journal of Haematology. 134: 613-5. PMID 16889615 DOI: 10.1111/J.1365-2141.2006.06237.X |
0.357 |
|
| 2006 |
Reader JC, Zhao XF, Butler MS, Rapoport AP, Ning Y. REL-positive double minute chromosomes in follicular lymphoma. Leukemia. 20: 1624-6. PMID 16775615 DOI: 10.1038/Sj.Leu.2404289 |
0.695 |
|
| 2006 |
Farag SS, Archer KJ, Mrózek K, Ruppert AS, Carroll AJ, Vardiman JW, Pettenati MJ, Baer MR, Qumsiyeh MB, Koduru PR, Ning Y, Mayer RJ, Stone RM, Larson RA, et al. Pretreatment cytogenetics add to other prognostic factors predicting complete remission and long-term outcome in patients 60 years of age or older with acute myeloid leukemia: results from Cancer and Leukemia Group B 8461. Blood. 108: 63-73. PMID 16522815 DOI: 10.1182/Blood-2005-11-4354 |
0.358 |
|
| 2006 |
Crowley JA, Wang Y, Rapoport AP, Ning Y. Detection of MOZ-CBP fusion in acute myeloid leukemia with 8;16 translocation. Leukemia. 19: 2344-5. PMID 16193081 DOI: 10.1038/Sj.Leu.2403971 |
0.382 |
|
| 2006 |
Badros AZ, Goloubeva O, Chumsri S, Ruehle K, Ning Y, Meekins J, Guedez L, Rapoport AP, Meisenberg B, Akpek G, Yanovich S, Sausville E. Clinical Presentation, Prognostic Factors and Treatment Outcome of Multiple Myeloma (MM) in African American (AA) Patients. Blood. 108: 5024-5024. DOI: 10.1182/Blood.V108.11.5024.5024 |
0.318 |
|
| 2005 |
Crowley JA, Butler MS, Ronnenburg MJ, Ament CN, Meekins JS, Ning Y. Development of a dual-color fluorescence in situ hybridization probe set on chromosome 6q to improve cytogenetic diagnosis of lymphoid malignancies. Cancer Genetics and Cytogenetics. 157: 78-81. PMID 15676153 DOI: 10.1016/J.Cancergencyto.2004.06.008 |
0.495 |
|
| 2004 |
Thomas L, Stamberg J, Gojo I, Ning Y, Rapoport AP. Double minute chromosomes in monoblastic (M5) and myeloblastic (M2) acute myeloid leukemia: two case reports and a review of literature. American Journal of Hematology. 77: 55-61. PMID 15307107 DOI: 10.1002/Ajh.20151 |
0.393 |
|
| 2003 |
Ning Y, Xu JF, Li Y, Chavez L, Riethman HC, Lansdorp PM, Weng NP. Telomere length and the expression of natural telomeric genes in human fibroblasts. Human Molecular Genetics. 12: 1329-36. PMID 12761048 DOI: 10.1093/Hmg/Ddg139 |
0.379 |
|
| 2000 |
Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, Hudson TJ, Riethman HC, Ledbetter DH, et al. An optimized set of human telomere clones for studying telomere integrity and architecture. American Journal of Human Genetics. 67: 320-32. PMID 10869233 DOI: 10.1086/302998 |
0.398 |
|
| 2000 |
Parshad R, Ning Y, Sanford KK. Suppression of X-ray-induced chromatid breaks in human tumor cells by introduction of normal chromosome 4. Cancer Genetics and Cytogenetics. 118: 72-5. PMID 10731596 DOI: 10.1016/S0165-4608(99)00177-6 |
0.35 |
|
| 2000 |
Rosenberg MJ, Vaske D, Killoran CE, Ning Y, Wargowski D, Hudgins L, Tifft CJ, Meck J, Blancato JK, Rosenbaum K, Pauli RM, Weber J, Biesecker LG. Detection of chromosomal aberrations by a whole-genome microsatellite screen American Journal of Human Genetics. 66: 419-427. PMID 10677301 DOI: 10.1086/302743 |
0.376 |
|
| 1999 |
Huang B, Wang S, Ning Y, Lamb AN, Bartley J. Autosomal XX sex reversal caused by duplication of SOX9. American Journal of Medical Genetics. 87: 349-53. PMID 10588843 DOI: 10.1002/(Sici)1096-8628(19991203)87:4<349::Aid-Ajmg13>3.0.Co;2-N |
0.393 |
|
| 1999 |
Liang JC, Ning Y, Wang RY, Padilla-Nash HM, Schröck E, Soenksen D, Nagarajan L, Ried T. Spectral karyotypic study of the HL-60 cell line: detection of complex rearrangements involving chromosomes 5, 7, and 16 and delineation of critical region of deletion on 5q31.1. Cancer Genetics and Cytogenetics. 113: 105-9. PMID 10484974 DOI: 10.1016/S0165-4608(99)00030-8 |
0.483 |
|
| 1999 |
Ning Y, Laundon CH, Schröck E, Buchanan P, Ried T. Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping. Prenatal Diagnosis. 19: 480-2. PMID 10360520 DOI: 10.1002/(Sici)1097-0223(199905)19:5<480::Aid-Pd547>3.0.Co;2-H |
0.439 |
|
| 1999 |
Bertram MJ, Bérubé NG, Hang-Swanson X, Ran Q, Leung JK, Bryce S, Spurgers K, Bick RJ, Baldini A, Ning Y, Clark LJ, Parkinson EK, Barrett JC, Smith JR, Pereira-Smith OM. Identification of a gene that reverses the immortal phenotype of a subset of cells and is a member of a novel family of transcription factor-like genes. Molecular and Cellular Biology. 19: 1479-85. PMID 9891081 DOI: 10.1128/Mcb.19.2.1479 |
0.375 |
|
| 1998 |
Huang B, Ning Y, Lamb AN, Sandlin CJ, Jamehdor M, Ried T, Bartley J. Identification of an unusual marker chromosome by spectral karyotyping. American Journal of Medical Genetics. 80: 368-72. PMID 9856565 DOI: 10.1002/(Sici)1096-8628(19981204)80:4<368::Aid-Ajmg12>3.0.Co;2-B |
0.43 |
|
| 1998 |
Phelan MC, Blackburn W, Rogers RC, Crawford EC, Cooley NR, Schrock E, Ning Y, Ried T. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Prenatal Diagnosis. 18: 1174-80. PMID 9854728 DOI: 10.1002/(Sici)1097-0223(199811)18:11<1174::Aid-Pd411>3.0.Co;2-H |
0.428 |
|
| 1998 |
Ried T, Schröck E, Ning Y, Wienberg J. Chromosome painting: a useful art. Human Molecular Genetics. 7: 1619-26. PMID 9735383 DOI: 10.1093/Hmg/7.10.1619 |
0.435 |
|
| 1998 |
Knutsen T, Mickley LA, Ried T, Green ED, du Manoir S, Schröck E, Macville M, Ning Y, Robey R, Polymeropoulos M, Torres R, Fojo T. Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL. Genes, Chromosomes & Cancer. 23: 44-54. PMID 9713996 DOI: 10.1002/(Sici)1098-2264(199809)23:1<44::Aid-Gcc7>3.0.Co;2-6 |
0.454 |
|
| 1998 |
Ning Y, Liang JC, Nagarajan L, Schröck E, Ried T. Characterization of 5q deletions by subtelomeric probes and spectral karyotyping. Cancer Genetics and Cytogenetics. 103: 170-2. PMID 9614919 DOI: 10.1016/S0165-4608(97)00417-2 |
0.416 |
|
| 1998 |
Schröck E, Veldman T, Padilla-Nash H, Ning Y, Spurbeck J, Jalal S, Shaffer LG, Papenhausen P, Kozma C, Phelan MC, Kjeldsen E, Schonberg SA, O'Brien P, Biesecker L, du Manoir S, et al. Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities. Human Genetics. 101: 255-62. PMID 9439652 DOI: 10.1007/S004390050626 |
0.438 |
|
| 1998 |
Rao PH, Cigudosa JC, Ning Y, Calasanz MJ, Iida S, Tagawa S, Michaeli J, Klein B, Dalla-Favera R, Jhanwar SC, Ried T, Chaganti RSK. Multicolor Spectral Karyotyping Identifies New Recurring Breakpoints and Translocations in Multiple Myeloma Blood. 92: 1743-1748. DOI: 10.1182/Blood.V92.5.1743 |
0.485 |
|
| 1996 |
Stone D, Ning Y, Guan XY, Kaiser-Kupfer M, Wynshaw-Boris A, Biesecker L. Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis. Human Genetics. 98: 396-402. PMID 8792811 DOI: 10.1007/S004390050228 |
0.444 |
|
| 1996 |
Ning Y, Roschke A, Smith ACM, Macha M, Precht K, Riethman H.Ledbetter DH, Flint J, Horsley S, Regan R, Kearney L, Knight S, Kvalov K, Brown WRA. A complete set of human telomeric probes and their clinical application Nature Genetics. 14: 86-89. PMID 8782825 DOI: 10.1038/Ng0996-86 |
0.445 |
|
| 1996 |
Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Ried T. Multicolor spectral karyotyping of human chromosomes. Science (New York, N.Y.). 273: 494-7. PMID 8662537 DOI: 10.1126/Science.273.5274.494 |
0.407 |
|
| 1996 |
Ning Y, Rosenberg M, Biesecker LG, Ledbetter DH. Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities. Human Genetics. 97: 765-9. PMID 8641694 DOI: 10.1007/Bf02346187 |
0.467 |
|
| 1996 |
Ning Y, Rosenberg M, Biesecker LG, Ledbetter DH. Isolation of the human chromosome 22q telomere and its application to detection of cryptic chromosomal abnormalities Human Genetics. 97: 765-769. DOI: 10.1007/s004390050134 |
0.338 |
|
| 1995 |
Biesecker LG, Rosenberg M, Dziadzio L, Ledbetter DH, Ning Y, Sarneso C, Rosenbaum K. Detection of a subtle rearrangement of chromosome 22 using molecular techniques. American Journal of Medical Genetics. 58: 389-394. PMID 8533859 DOI: 10.1002/Ajmg.1320580426 |
0.406 |
|
| 1994 |
Noda A, Ning Y, Venable SF, Pereira-Smith OM, Smith JR. Cloning of senescent cell-derived inhibitors of DNA synthesis using an expression screen Experimental Cell Research. 211: 90-98. PMID 8125163 DOI: 10.1006/Excr.1994.1063 |
0.313 |
|
| 1993 |
Ning Y, Lovell M, Cooley LD, Pereira-Smith OM. "PCR Karyotype" of Monochromosomal Somatic Cell Hybrids Genomics. 16: 758-760. PMID 8325652 DOI: 10.1006/Geno.1993.1260 |
0.426 |
|
| 1992 |
Ning Y, Lovell M, Taylor L, Pereira-Smith OM. Isolation of monochromosomal hybrids following fusion of human diploid fibroblast-derived microcells with mouse A9 cells. Cytogenetic and Genome Research. 60: 79-80. PMID 1582264 DOI: 10.1159/000133300 |
0.347 |
|
| 1992 |
Pereira-Smith OM, Ning Y. Molecular genetic studies of cellular senescence Experimental Gerontology. 27: 519-522. PMID 1426085 DOI: 10.1016/0531-5565(92)90006-L |
0.338 |
|
| 1991 |
Ning Y, Weber JL, Killary AM, Ledbetter DH, Smith JR, Pereira-Smith OM. Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4. Proceedings of the National Academy of Sciences of the United States of America. 88: 5635-9. PMID 2062841 DOI: 10.1073/Pnas.88.13.5635 |
0.397 |
|
| 1991 |
Ning Y, Pereira-Smith OM. Molecular genetic approaches to the study of cellular senescence Mutation Research Dnaging. 256: 303-310. PMID 1722020 DOI: 10.1016/0921-8734(91)90021-3 |
0.391 |
|
| 1991 |
Ning Y, Shay JW, Lovell M, Taylor L, Ledbetter DH, Pereira-Smith OM. Tumor suppression by chromosome 11 is not due to cellular senescence. Experimental Cell Research. 192: 220-6. PMID 1670600 DOI: 10.1016/0014-4827(91)90179-X |
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| 1990 |
Pereira-Smith OM, Robetorye S, Ning Y, Orson FM. Hybrids from fusion of normal human T lymphocytes with immortal human cells exhibit limited life span. Journal of Cellular Physiology. 144: 546-9. PMID 2391382 DOI: 10.1002/Jcp.1041440324 |
0.357 |
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