| Year |
Citation |
Score |
| 2018 |
Cheng H, Yang X, Si H, Saleh AD, Xiao W, Coupar J, Gollin SM, Ferris RL, Issaeva N, Yarbrough WG, Prince ME, Carey TE, Van Waes C, Chen Z. Genomic and Transcriptomic Characterization Links Cell Lines with Aggressive Head and Neck Cancers. Cell Reports. 25: 1332-1345.e5. PMID 30380422 DOI: 10.1016/j.celrep.2018.10.007 |
0.405 |
|
| 2018 |
Achkar T, Ali SM, Welsh A, Dhir R, Gollin SM, Parikh RA. A Prolonged Response to Platinum-Based Therapy in a Patient with Metastatic Urothelial Carcinoma Harboring a Single Rearranged and Truncated NF2 Gene. Genes, Chromosomes & Cancer. PMID 29532557 DOI: 10.1002/Gcc.22537 |
0.65 |
|
| 2016 |
Kaseb HO, Fohrer-Ting H, Lewis DW, Lagasse E, Gollin SM. IDENTIFICATION, EXPANSION AND CHARACTERIZATION OF CANCER CELLS WITH STEM CELL PROPERTIES FROM HEAD AND NECK SQUAMOUS CELL CARCINOMAS. Experimental Cell Research. PMID 27619333 DOI: 10.1016/J.Yexcr.2016.09.003 |
0.419 |
|
| 2016 |
Kaseb HO, Lewis DW, Saunders WS, Gollin SM. Cell division patterns and chromosomal segregation defects in oral cancer stem cells. Genes, Chromosomes & Cancer. PMID 27123539 DOI: 10.1002/gcc.22371 |
0.453 |
|
| 2014 |
Gollin SM. Cytogenetic alterations and their molecular genetic correlates in head and neck squamous cell carcinoma: a next generation window to the biology of disease. Genes, Chromosomes & Cancer. 53: 972-90. PMID 25183546 DOI: 10.1002/gcc.22214 |
0.424 |
|
| 2014 |
Gollin SM, Reshmi SC. Janet Davison Rowley, M.D. (1925–2013). American Journal of Human Genetics. 94: 805-8. PMID 25035867 DOI: 10.1016/J.Ajhg.2014.05.008 |
0.553 |
|
| 2014 |
Sankunny M, Parikh RA, Lewis DW, Gooding WE, Saunders WS, Gollin SM. Targeted inhibition of ATR or CHEK1 reverses radioresistance in oral squamous cell carcinoma cells with distal chromosome arm 11q loss. Genes, Chromosomes & Cancer. 53: 129-43. PMID 24327542 DOI: 10.1002/Gcc.22125 |
0.761 |
|
| 2014 |
Parikh RA, Appleman LJ, Bauman JE, Sankunny M, Lewis DW, Vlad A, Gollin SM. Upregulation of the ATR-CHEK1 pathway in oral squamous cell carcinomas. Genes, Chromosomes & Cancer. 53: 25-37. PMID 24142626 DOI: 10.1002/Gcc.22115 |
0.739 |
|
| 2011 |
Wu Z, Doondeea JB, Gholami AM, Janning MC, Lemeer S, Kramer K, Eccles SA, Gollin SM, Grenman R, Walch A, Feller SM, Kuster B. Quantitative chemical proteomics reveals new potential drug targets in head and neck cancer Molecular and Cellular Proteomics. 10. PMID 21955398 DOI: 10.1074/mcp.M111.011635 |
0.311 |
|
| 2011 |
Shiwarski D, Bertrand C, Egloff AM, Huang X, Seethala R, Grandis J, Gollin S, Duvvuri U. Abstract LB-220: TMEM16A, a novel calcium-activated chloride channel, modulates tumor proliferation via MAPK and Cyclin-D1 signaling Cancer Research. 71. DOI: 10.1158/1538-7445.Am2011-Lb-220 |
0.432 |
|
| 2010 |
Henson BJ, Gollin SM. Overexpression of KLF13 and FGFR3 in oral cancer cells. Cytogenetic and Genome Research. 128: 192-8. PMID 20539070 DOI: 10.1159/000308303 |
0.303 |
|
| 2009 |
Gollin S, Sankunny M, Flores-Obando R, Huang X, Parikh R. O46. Reversal of resistance to standard therapy in oral squamous cell carcinoma cells by RNA interference Oral Oncology Supplement. 3: 72. DOI: 10.1016/J.Oos.2009.06.131 |
0.702 |
|
| 2008 |
Odoux C, Fohrer H, Hoppo T, Guzik L, Stolz DB, Lewis DW, Gollin SM, Gamblin TC, Geller DA, Lagasse E. A stochastic model for cancer stem cell origin in metastatic colon cancer. Cancer Research. 68: 6932-41. PMID 18757407 DOI: 10.1158/0008-5472.Can-07-5779 |
0.327 |
|
| 2008 |
Martin CL, Reshmi SC, Ried T, Gottberg W, Wilson JW, Reddy JK, Khanna P, Johnson JT, Myers EN, Gollin SM. Chromosomal imbalances in oral squamous cell carcinoma: Examination of 31 cell lines and review of the literature Oral Oncology. 44: 369-382. PMID 17681875 DOI: 10.1016/J.Oraloncology.2007.05.003 |
0.746 |
|
| 2007 |
Sun Q, Sakaida T, Yue W, Gollin SM, Yu J. Chemosensitization of head and neck cancer cells by PUMA. Molecular Cancer Therapeutics. 6: 3180-8. PMID 18089712 DOI: 10.1158/1535-7163.Mct-07-0265 |
0.35 |
|
| 2007 |
Parikh RA, White JS, Huang X, Schoppy DW, Baysal BE, Baskaran R, Bakkenist CJ, Saunders WS, Hsu LC, Romkes M, Gollin SM. Loss of distal 11q is associated with DNA repair deficiency and reduced sensitivity to ionizing radiation in head and neck squamous cell carcinoma. Genes, Chromosomes & Cancer. 46: 761-75. PMID 17492757 DOI: 10.1002/Gcc.20462 |
0.718 |
|
| 2007 |
Lin CJ, Grandis JR, Carey TE, Gollin SM, Whiteside TL, Koch WM, Ferris RL, Lai SY. Head and neck squamous cell carcinoma cell lines: established models and rationale for selection. Head & Neck. 29: 163-88. PMID 17312569 DOI: 10.1002/Hed.20478 |
0.381 |
|
| 2007 |
Reshmi SC, Roychoudhury S, Yu Z, Feingold E, Potter D, Saunders WS, Gollin SM. Inverted duplication pattern in anaphase bridges confirms the breakage-fusion-bridge (BFB) cycle model for 11q13 amplification. Cytogenetic and Genome Research. 116: 46-52. PMID 17268177 DOI: 10.1159/000097425 |
0.726 |
|
| 2007 |
Gollin SM. Mechanisms leading to nonrandom, nonhomologous chromosomal translocations in leukemia. Seminars in Cancer Biology. 17: 74-9. PMID 17157028 DOI: 10.1016/j.semcancer.2006.10.002 |
0.32 |
|
| 2007 |
White JS, Weissfeld JL, Ragin CC, Rossie KM, Martin CL, Shuster M, Ishwad CS, Law JC, Myers EN, Johnson JT, Gollin SM. The influence of clinical and demographic risk factors on the establishment of head and neck squamous cell carcinoma cell lines. Oral Oncology. 43: 701-12. PMID 17112776 DOI: 10.1016/J.Oraloncology.2006.09.001 |
0.424 |
|
| 2007 |
Reshmi SC, Huang X, Schoppy DW, Black RC, Saunders WS, Smith DI, Gollin SM. Relationship between FRA11F and 11q13 gene amplification in oral cancer. Genes, Chromosomes & Cancer. 46: 143-54. PMID 17099871 DOI: 10.1002/Gcc.20394 |
0.728 |
|
| 2007 |
Mondal G, Sengupta S, Panda CK, Gollin SM, Saunders WS, Roychoudhury S. Overexpression of Cdc20 leads to impairment of the spindle assembly checkpoint and aneuploidization in oral cancer. Carcinogenesis. 28: 81-92. PMID 16777988 DOI: 10.1093/Carcin/Bgl100 |
0.448 |
|
| 2006 |
Huang X, Godfrey TE, Gooding WE, McCarty KS, Gollin SM. Comprehensive genome and transcriptome analysis of the 11q13 amplicon in human oral cancer and synteny to the 7F5 amplicon in murine oral carcinoma. Genes, Chromosomes & Cancer. 45: 1058-69. PMID 16906560 DOI: 10.1002/Gcc.20371 |
0.414 |
|
| 2006 |
Hsu LC, Huang X, Seasholtz S, Potter DM, Gollin SM. Gene amplification and overexpression of protein phosphatase 1alpha in oral squamous cell carcinoma cell lines. Oncogene. 25: 5517-26. PMID 16619035 DOI: 10.1038/sj.onc.1209563 |
0.428 |
|
| 2006 |
Wittschieben JP, Reshmi SC, Gollin SM, Wood RD. Loss of DNA polymerase zeta causes chromosomal instability in mammalian cells. Cancer Research. 66: 134-42. PMID 16397225 DOI: 10.1158/0008-5472.Can-05-2982 |
0.689 |
|
| 2006 |
Gollin SM, Parikh RA, White JS, Huang X, Baskaran R, Saunders WS, Bakkenist CJ, Reshmi SC. S041 Identification of the Mechanism of 11q13 Amplification Leads to Detection of DNA Repair Defects in HNSCC Cell Lines Archives of Otolaryngology–Head & Neck Surgery. 132: 848. DOI: 10.1001/Archotol.132.8.848-A |
0.742 |
|
| 2006 |
Duvvuri UU, Henson BJ, Huang X, White JS, Parikh RA, Seethala R, Grandis JR, Gollin SM. S038 Characterization of TMEM16A in Squamous Cell Carcinoma of the Head and Neck Archives of Otolaryngology–Head & Neck Surgery. 132: 847. DOI: 10.1001/Archotol.132.8.847-A |
0.628 |
|
| 2005 |
Cook JR, Aguilera NI, Reshmi S, Huang X, Yu Z, Gollin SM, Abbondanzo SL, Swerdlow SH. Deletion 6q is not a characteristic marker of nodal lymphoplasmacytic lymphoma. Cancer Genetics and Cytogenetics. 162: 85-8. PMID 16157207 DOI: 10.1016/J.Cancergencyto.2005.04.013 |
0.656 |
|
| 2005 |
Reshmi SC, Gollin SM. Chromosomal instability in oral cancer cells. Journal of Dental Research. 84: 107-17. PMID 15668327 DOI: 10.1177/154405910508400203 |
0.7 |
|
| 2005 |
Gollin SM. Mechanisms leading to chromosomal instability. Seminars in Cancer Biology. 15: 33-42. PMID 15613286 DOI: 10.1016/j.semcancer.2004.09.004 |
0.413 |
|
| 2004 |
Reshmi SC, Saunders WS, Kudla DM, Ragin CR, Gollin SM. Chromosomal instability and marker chromosome evolution in oral squamous cell carcinoma. Genes, Chromosomes & Cancer. 41: 38-46. PMID 15236315 DOI: 10.1002/Gcc.20064 |
0.723 |
|
| 2004 |
Hewitt C, Wilson P, McGlinn E, MacFarlane G, Papageorgiou A, Woodwards RT, Sloan P, Gollin SM, Paterson I, Parkinson KK, Read AP, Thakker N. DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinoma. Cancer Letters. 209: 207-13. PMID 15159023 DOI: 10.1016/j.canlet.2003.12.018 |
0.46 |
|
| 2004 |
Hoffelder DR, Luo L, Burke NA, Watkins SC, Gollin SM, Saunders WS. Resolution of anaphase bridges in cancer cells. Chromosoma. 112: 389-97. PMID 15156327 DOI: 10.1007/S00412-004-0284-6 |
0.411 |
|
| 2004 |
Ragin CC, Reshmi SC, Gollin SM. Mapping and analysis of HPV16 integration sites in a head and neck cancer cell line. International Journal of Cancer. Journal International Du Cancer. 110: 701-9. PMID 15146560 DOI: 10.1002/Ijc.20193 |
0.649 |
|
| 2004 |
Reing JE, Gollin SM, Saunders WS. The occurrence of chromosome segregational defects is an intrinsic and heritable property of oral squamous cell carcinoma cell lines. Cancer Genetics and Cytogenetics. 150: 57-61. PMID 15041224 DOI: 10.1016/j.cancergencyto.2003.08.002 |
0.449 |
|
| 2004 |
Gollin SM. Chromosomal instability. Current Opinion in Oncology. 16: 25-31. PMID 14685089 |
0.336 |
|
| 2003 |
Toomes C, Jackson A, Maguire K, Wood J, Gollin S, Ishwad C, Paterson I, Prime S, Parkinson K, Bell S, Woods G, Markham A, Oliver R, Woodward R, Sloan P, et al. The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis. Genes, Chromosomes & Cancer. 37: 132-40. PMID 12696061 DOI: 10.1002/Gcc.10191 |
0.5 |
|
| 2003 |
Reshmi-Skarja S, Huebner A, Handschug K, Finegold DN, Clark AJ, Gollin SM. Chromosomal fragility in patients with triple A syndrome. American Journal of Medical Genetics. Part A. 117: 30-6. PMID 12548737 DOI: 10.1002/ajmg.a.10846 |
0.324 |
|
| 2002 |
Hu J, McPherson E, Surti U, Hasegawa SL, Gunawardena S, Gollin SM. Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors. American Journal of Medical Genetics. 113: 82-8. PMID 12400070 DOI: 10.1002/ajmg.10708 |
0.366 |
|
| 2002 |
Huang X, Gollin SM, Raja S, Godfrey TE. High-resolution mapping of the 11q13 amplicon and identification of a gene, TAOS1, that is amplified and overexpressed in oral cancer cells. Proceedings of the National Academy of Sciences of the United States of America. 99: 11369-74. PMID 12172009 DOI: 10.1073/pnas.172285799 |
0.365 |
|
| 2001 |
Gollin SM. Chromosomal alterations in squamous cell carcinomas of the head and neck: window to the biology of disease. Head & Neck. 23: 238-53. PMID 11428456 DOI: 10.1002/1097-0347(200103)23:3<238::AID-HED1025>3.0.CO;2-H |
0.408 |
|
| 2001 |
Rao UNM, Gollin SM, Beaves S, Cieply K, Nalesnik M, Michalopoulos GK. Comparative genomic hybridization of hepatocellular carcinoma: Correlation with fluorescence In Situ hybridization in paraffin-embedded tissue Molecular Diagnosis. 6: 27-37. PMID 11257209 DOI: 10.1054/Modi.2001.22021 |
0.383 |
|
| 2000 |
Shuster MI, Han L, Le Beau MM, Davis E, Sawicki M, Lese CM, Park NH, Colicelli J, Gollin SM. A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification. Genes, Chromosomes & Cancer. 28: 153-63. PMID 10825000 DOI: 10.1002/(Sici)1098-2264(200006)28:2<153::Aid-Gcc4>3.0.Co;2-9 |
0.496 |
|
| 2000 |
Saunders WS, Shuster M, Huang X, Gharaibeh B, Enyenihi AH, Petersen I, Gollin SM. Chromosomal instability and cytoskeletal defects in oral cancer cells. Proceedings of the National Academy of Sciences of the United States of America. 97: 303-8. PMID 10618413 DOI: 10.1073/pnas.97.1.303 |
0.456 |
|
| 1999 |
Ishwad CS, Shuster M, Bockmühl U, Thakker N, Shah P, Toomes C, Dixon M, Ferrell RE, Gollin SM. Frequent allelic loss and homozygous deletion in chromosome band 8p23 in oral cancer. International Journal of Cancer. Journal International Du Cancer. 80: 25-31. PMID 9935225 DOI: 10.1002/(Sici)1097-0215(19990105)80:1<25::Aid-Ijc6>3.0.Co;2-G |
0.481 |
|
| 1998 |
Baysal BE, Potkin SG, Farr JE, Higgins MJ, Korcz J, Gollin SM, James MR, Evans GA, Richard CW. Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree. American Journal of Medical Genetics. 81: 81-91. PMID 9514593 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<81::Aid-Ajmg15>3.0.Co;2-S |
0.305 |
|
| 1997 |
Shuster M, Comsa S, Reddy J, Rossie K, Johnson J, Gollin S. Fish analysis of the CDKN2/p16 gene in oral squamous cell carcinoma (OSCC) Cancer Genetics and Cytogenetics. 98: 166. DOI: 10.1016/S0165-4608(97)90307-1 |
0.346 |
|
| 1996 |
Virgilio L, Shuster M, Gollin SM, Veronese ML, Ohta M, Huebner K, Croce CM. FHIT gene alterations in head and neck squamous cell carcinomas. Proceedings of the National Academy of Sciences of the United States of America. 93: 9770-5. PMID 8790406 DOI: 10.1073/Pnas.93.18.9770 |
0.437 |
|
| 1996 |
Ishwad CS, Ferrell RE, Rossie KM, Appel BN, Johnson JT, Myers EN, Law JC, Srivastava S, Gollin SM. Loss of heterozygosity of the short arm of chromosomes 3 and 9 in oral cancer International Journal of Cancer. 69: 1-4. PMID 8600052 DOI: 10.1002/(Sici)1097-0215(19960220)69:1<1::Aid-Ijc1>3.0.Co;2-8 |
0.379 |
|
| 1995 |
Lese CM, Rossie KM, Appel BN, Reddy JK, Johnson JT, Myers EN, Gollin SM. Visualization of INT2 and HST1 amplification in oral squamous cell carcinomas Genes Chromosomes and Cancer. 12: 288-295. PMID 7539284 DOI: 10.1002/gcc.2870120409 |
0.508 |
|
| 1995 |
Gollin S, Lese C, Ishwad C, Law J, Ferrell R. Converging classical cytogenetic, molecular cytogenetic, and molecular genetic analyses of oral squamous cell carcinoma Cancer Genetics and Cytogenetics. 84: 140. DOI: 10.1016/0165-4608(96)85248-4 |
0.313 |
|
| 1994 |
Randhawa PS, Zeevi A, Alvares C, Gollin S, Agostini R, Yunis E, Saidman S, Contis L, Demetris AJ, Nalesnik MA. Morphologic and immunophenotypic characterization of a cell line derived from liver tissue with Epstein-Barr virus associated post-transplant lymphoproliferative disease. In Vitro Cellular & Developmental Biology. Animal. 400-6. PMID 8087305 DOI: 10.1007/Bf02634361 |
0.401 |
|
| 1993 |
Sankary S, Sherwin RN, Malone PS, Janecka I, Barnes L, Storto PD, Gollin SM. Clonal chromosomal aberrations in a leiomyosarcoma of the sinonasal tract. Cancer Genetics and Cytogenetics. 65: 21-6. PMID 8431912 DOI: 10.1016/0165-4608(93)90053-O |
0.359 |
|
| 1992 |
Gollin SM, Storto PD, Malone PS, Barnes L, Washington JA, Chidambaram A, Janecka IP. Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma Genes Chromosomes and Cancer. 4: 146-152. PMID 1373315 DOI: 10.1002/gcc.2870040208 |
0.361 |
|
| 1992 |
Shimizu Y, Demetris AJ, Gollin SM, Storto PD, Bedford HM, Altarac S, Iwatsuki S, Herberman RB, Whiteside TL. Two new human cholangiocarcinoma cell lines and their cytogenetics and responses to growth factors, hormones, cytokines or immunologic effector cells. International Journal of Cancer. 52: 252-60. PMID 1355757 DOI: 10.1002/ijc.2910520217 |
0.337 |
|
| 1991 |
Storto PD, Saidman SL, Demetris AJ, Letessier E, Whiteside TL, Gollin SM. Chromosomal breakpoints in cholangiocarcinoma cell lines. Genes, Chromosomes & Cancer. 2: 300-10. PMID 2176543 DOI: 10.1002/gcc.2870020408 |
0.456 |
|
| 1988 |
Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH. Duplication of proximal 15q as a cause of Prader-Willi syndrome. American Journal of Medical Genetics. 28: 791-802. PMID 3688017 DOI: 10.1002/Ajmg.1320280403 |
0.312 |
|
| 1986 |
Gollin SM, Perrot LJ, Gray BA, Kletzel M. Spontaneous expression of fra(11)(q23) in a patient with Ewing's sarcoma and t(11;22)(q23;q11). Cancer Genetics and Cytogenetics. 20: 331-9. PMID 3943071 DOI: 10.1016/0165-4608(86)90092-0 |
0.344 |
|
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