S. Gollin

发表

Variation of p53 mutational spectra between carcinoma of the upper and lower respiratory tract.

S. Srivastava, J. Johnson, J. Weissfeld, 1995, Clinical cancer research : an official journal of the American Association for Cancer Research.

Transcript map of the 8p23 putative tumor suppressor region.

R. Uppaluri, S. Scholnick, S. Gollin, 2001, Genomics.

Mitosis: Chromosomal Rearrangements

S. Gollin, Shalini Reshmi Skarja, 2006 .

Splenic small B-cell lymphoma with IGH/BCL3 translocation.

S. Swerdlow, S. Gollin, R. Ketterling, 2006, Human pathology.

Interlaboratory study to validate a STR profiling method for intraspecies identification of mouse cell lines

Erin M Hall, S. Lund, J. Almeida, 2019, PloS one.

Cell cycle-specific changes in the ultrastructural organization of prematurely condensed chromosomes

S. Hanks, W. Hittelman, S. Gollin, 1983, Chromosoma.

A multisample chamber for dehydration and critical point drying

S. Gollin, W. Wray, 1984 .

Isopycnic centrifugation of mammalian metaphase chromosomes in Nycodenz.

S. Gollin, W. Wray, 1984, Experimental cell research.

A porcine model of phenylketonuria generated by CRISPR/Cas9 genome editing

Sarah A. Hansen, S. Christ, L. Spate, 2020, JCI insight.

Genomic and Transcriptomic Characterization Links Cell Lines with Aggressive Head and Neck Cancers

W. Xiao, R. Ferris, C. Van Waes, 2018, Cell reports.

Knowledge about human papillomavirus and the HPV vaccine – a survey of the general population

Erin A. Jones, D. Heron, E. Taioli, 2009, Infectious Agents and Cancer.

Biology, cytogenetics, and sensitivity to immunological effector cells of new head and neck squamous cell carcinoma lines.

C. Snyderman, J. Johnson, T. Whiteside, 1989, Cancer research.

Variation of p 53 Mutational Spectra between Carcinoma of the Upper and Lower Respiratory Tract

S. Srivastava, J. Weissfeld, R. Ferrell, 2005 .

Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.

U. Surti, S. Gollin, E. McPherson, 2002, American journal of medical genetics.

Myeloperoxidase-Dependent Oxidation of Etoposide in Human Myeloid Progenitor CD34+ Cells

S. Gollin, V. Kagan, I. I. Vlasova, 2011, Molecular Pharmacology.

A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage‐fusion‐bridge cycle model for 11q13 amplification

M. L. Le Beau, M. Sawicki, N. Park, 2000, Genes, chromosomes & cancer.

Visualization of INT2 and HST1 Amplification in oral squamous cell carcinomas

S. Gollin, E. Myers, K. Rossie, 1995, Genes, chromosomes & cancer.

In vitro culture of B-lymphocytes derived from epstein-barr-virus-associated posttransplant lymphoproliferative disease: Cytokine production and effect of interferon-alpha

J. Locker, S. Gollin, J. Demetris, 1997, In Vitro Cellular & Developmental Biology - Animal.

Parental Alleles of an Imprinted Mouse Transgene Replicate Synchronously

S. Gollin, D. Olins, A. Olins, 1998 .

Chromosomal breakpoints in cholangiocarcinoma cell lines

T. Whiteside, S. Saidman, S. Gollin, 1990, Genes, chromosomes & cancer.

Imprinted Gene for Familial Nonchromaffin

M. James, G. Evans, W. Rubinstein, 2006 .

Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma

S. Gollin, A. Chidambaram, L. Barnes, 1992, Genes, chromosomes & cancer.

Insulin secretion deficits in a Prader-Willi syndrome β-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperones

Simon C Watkins, J. Diedrich, J. Yates, 2022, bioRxiv.

Fluorescence Immunophenotypic and Interphase Cytogenetic Characterization of Nodal Lymphoplasmacytic Lymphoma

U. Surti, S. Swerdlow, S. Gollin, 2008, The American journal of surgical pathology.

Mechanisms leading to nonrandom, nonhomologous chromosomal translocations in leukemia.

S. Gollin, 2007, Seminars in cancer biology.

Defining the borders of splenic marginal zone lymphoma: a multiparameter study.

U. Surti, S. Swerdlow, S. Gollin, 2010, Human pathology.

The Genomic Landscape of PAX5, IKZF1, and CDKN2A/B Alterations in B-Cell Precursor Acute Lymphoblastic Leukemia

U. Surti, Z. Ou, S. Gollin, 2017, Cytogenetic and Genome Research.

Atypical (7;19) translocation in acute myelomonocytic leukemia.

S. Gollin, R. Joyce, J. Krause, 1991, Cancer genetics and cytogenetics.

Overexpression of KLF13 and FGFR3 in Oral Cancer Cells

S. Gollin, B. J. Henson, 2010, Cytogenetic and Genome Research.

Frequent allelic loss and homozygous deletion in chromosome band 8p23 in oral cancer

R. Ferrell, S. Gollin, C. Toomes, 1999, International journal of cancer.

Isolation and characterization of a human hepatic epithelial-like cell line (AKN-1) from a normal liver

S. Strom, S. Gansauge, A. Nussler, 1999, In Vitro Cellular & Developmental Biology - Animal.

Chromosomal instability

S. Gollin, 2004, Current opinion in oncology.

Gene amplification and overexpression of protein phosphatase 1α in oral squamous cell carcinoma cell lines

S. Gollin, L. Hsu, D. Potter, 2006, Oncogene.

Acute myeloblastic leukemia with a pericentric inversion of chromosome 6 in a child with Down syndrome.

S. Gollin, N. Wald, L. Penchansky, 1994, Cancer genetics and cytogenetics.

Head and neck squamous cell carcinoma cell lines.

S. Gollin, M. Sherer, 1992, Genes, chromosomes & cancer.

Morphologic, immunologic, biochemical, and cytogenetic characteristics of the human glioblastoma-derived cell line, SNB-19

K. Giuliano, W. Welch, S. Gollin, 1995, In Vitro Cellular & Developmental Biology - Animal.

Cytogenetics, Immunostaining for Fibroblast Growth Factors, p53 Sequencing, and Clinical Features of Two Cases of Cystosarcoma Phyllodes

S. Finkelstein, P. Woolley, S. Gollin, 2000, Molecular Diagnosis.

Chromosomal fragility in patients with triple A syndrome

S. Gollin, D. Finegold, A. Huebner, 2003, American journal of medical genetics. Part A.

A near-haploid bone marrow karyotype in systemic mast cell disease: is it characteristic of the disease or an incidental finding?

S. Swerdlow, S. Gollin, E. Ball, 1998, Cancer genetics and cytogenetics.

Acquired monosomy 7 in donor cells in a patient treated for acute lymphoblastic leukemia with bone marrow transplantation.

S. Swerdlow, S. Gollin, N. Wald, 1997, Cancer genetics and cytogenetics.

Chromosomal translocations in secondary acute myeloid leukemia.

J. Rowley, C. Rosenberg, S. Gollin, 1996, The New England journal of medicine.

Morphologic and immunophenotypic characterization of a cell line derived from liver tissue with epstein-barr virus associated post-transplant lymphoproliferative disease

S. Saidman, S. Gollin, A. Demetris, 1994, In Vitro Cellular & Developmental Biology - Animal.

Chronic myelogenous leukemia and acute lymphoblastic leukemia occurring in the course of polycythemia vera

S. Gollin, D. Przepiorka, P. Chervenick, 1993, American journal of hematology.

Quantitative Chemical Proteomics Reveals New Potential Drug Targets in Head and Neck Cancer*

Bernhard Kuster, Amin Moghaddas Gholami, Axel Walch, 2011, Molecular & Cellular Proteomics.

Comparative Genomic Hybridization of Hepatocellular Carcinoma: Correlation With Fluorescence In Situ Hybridization in Paraffin-embedded Tissue

G. Michalopoulos, S. Gollin, U. Rao, 2001, Molecular Diagnosis.

Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases.

J. Opitz, J. Carey, S. Gollin, 1987, American journal of medical genetics.

Comprehensive genome and transcriptome analysis of the 11q13 amplicon in human oral cancer and synteny to the 7F5 amplicon in murine oral carcinoma

T. Godfrey, S. Gollin, K. Mccarty, 2006, Genes, chromosomes & cancer.

Chromosomal alterations in squamous cell carcinomas of the head and neck: Window to the biology of disease

S. Gollin, 2001, Head & neck.

Head and neck squamous cell carcinoma cell lines: Established models and rationale for selection

J. Grandis, R. Ferris, T. Whiteside, 2007, Head & neck.

Viral load, gene expression and mapping of viral integration sites in HPV16‐associated HNSCC cell lines

E. Speel, T. Carey, S. Gollin, 2015, International journal of cancer.

Duplication of proximal 15q as a cause of Prader-Willi syndrome.

D. Ledbetter, S. Gollin, V. Riccardi, 1987, American journal of medical genetics.

Spindle Multipolarity Is Prevented by Centrosomal Clustering

S. Gollin, W. Saunders, J. Reing, 2005, Science.

Overexpression of glycosylphosphatidylinositol (GPI) transamidase subunits phosphatidylinositol glycan class T and/or GPI anchor attachment 1 induces tumorigenesis and contributes to invasion in human breast cancer.

Xin Huang, Aditi Chatterjee, David Sidransky, 2006, Cancer research.

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

A. Read, S. Gollin, M. Dixon, 2003, Genes, chromosomes & cancer.

Tumors of the Upper Aerodigestive Tract

S. Gollin, 2015 .

11. Tumors of the Upper Aerodigestive Tract

S. Gollin, Mihaela Avramut and, 2010 .

Immunomodulatory drugs downregulate IKZF1 leading to expansion of hematopoietic progenitors with concomitant block of megakaryocytic maturation

D. Stolz, S. Gollin, Jing Fu, 2018, Haematologica.

Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree.

M. James, S. Potkin, G. Evans, 1998, American journal of medical genetics.

Acquired chromosome abnormalities: the cytogenetics of cancer

S. Gollin, 2005 .

Resolution of anaphase bridges in cancer cells

Simon C Watkins, S. Gollin, W. Saunders, 2004, Chromosoma.

Correlation of Classic and Molecular Cytogenetic Alterations in Soft-Tissue Sarcomas: Analysis of 46 Tumors With Emphasis on Adipocytic Tumors and Synovial Sarcoma

Urvashi Surti, U. Surti, S. Gollin, 2017, Applied immunohistochemistry & molecular morphology : AIMM.

Somatic mutation and gain of copy number of PIK3CA in human breast cancer

Xin Huang, David Goldenberg, Aditi Chatterjee, 2005, Breast Cancer Research.

Chromosomal instability and marker chromosome evolution in oral squamous cell carcinoma

S. Gollin, W. Saunders, S. Reshmi, 2004, Genes, chromosomes & cancer.

Decreased expression of miR‐125b and miR‐100 in oral cancer cells contributes to malignancy

E. Feingold, S. Gollin, Samsiddhi Bhattacharjee, 2009, Genes, chromosomes & cancer.

Prevalence of HPV infection in racial–ethnic subgroups of head and neck cancer patients

K. Devarajan, C. Eng, E. Taioli, 2017, Carcinogenesis.

Prevalence of HPV infection in racial-ethnic subgroups of head and neck cancer patients.

K. Devarajan, C. Eng, E. Taioli, 2016, Carcinogenesis.

The p53–PUMA axis suppresses iPSC generation

S. Gollin, T. Cheng, Shi-Yuan Cheng, 2013, Nature Communications.

The Relationship between TPS 3 Mutations and Overexpression of p 53 and Prognosis in Malignant Gliomas of Childhood '

I. Pollack, S. Finkelstein, S. Gollin, 2022 .

Cytogenetics of cranial base tumors

S. Gollin, I. Janecka, 2005, Journal of Neuro-Oncology.

Uncommon mutation, but common amplifications, of the PIK3CA gene in thyroid tumors.

P. Ladenson, Guojun Wu, Zhongmin Guo, 2005, The Journal of clinical endocrinology and metabolism.

Myeloperoxidase-Dependent Oxidation of Etoposide in Human Myeloid Progenitor CD34 (cid:1) Cells

S. Gollin, V. Kagan, I. I. Vlasova, 2011 .

Chromosome abnormalities in familial hemophagocytic lymphohistiocytosis

S. Gollin, M. Kletzel, D. Berry, 1986, Cancer.

The influence of clinical and demographic risk factors on the establishment of head and neck squamous cell carcinoma cell lines.

C. Martin, J. Weissfeld, Jason S. White, 2007, Oral oncology.

Homogeneously Staining Regions

S. Gollin, 2013 .

Cell division patterns and chromosomal segregation defects in oral cancer stem cells

S. Gollin, W. Saunders, Hatem O. Kaseb, 2016, Genes, chromosomes & cancer.

High-resolution mapping of the 11q13 amplicon and identification of a gene, TAOS1, that is amplified and overexpressed in oral cancer cells

Xin Huang, Tony E Godfrey, T. Godfrey, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Integration of microarray analysis into the clinical diagnosis of hematological malignancies: How much can we improve cytogenetic testing?

U. Surti, S. Swerdlow, A. Rajkovic, 2015, Oncotarget.

DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinoma.

A. Read, S. Gollin, N. Thakker, 2004, Cancer letters.

Chromosomal imbalances in oral squamous cell carcinoma: examination of 31 cell lines and review of the literature.

Thomas Ried, Christa Lese Martin, C. Martin, 2008, Oral oncology.

Integration of high‐risk human papillomavirus into cellular cancer‐related genes in head and neck cancer cell lines

Erin McKean, B. Teh, R. Ferris, 2017, Head & neck.

Fatty acid synthase gene overexpression and copy number gain in prostate adenocarcinoma.

R. Dhir, U. Chandran, S. Gollin, 2006, Human pathology.

Trisomy 7 in synovial fibroblasts obtained from arthritic joints

S. Gollin, C. Evans, H. Georgescu, 1999, Inflammation Research.

Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites

U. Surti, A. Parwani, S. Gollin, 2007, Diagnostic pathology.

Spontaneous expression of fra(11)(q23) in a patient with Ewing's sarcoma and t(11;22)(q23;q11).

S. Gollin, L. J. Perrot, B. Gray, 1986, Cancer genetics and cytogenetics.

Mechanisms leading to chromosomal instability.

S. Gollin, 2005, Seminars in cancer biology.

Prevalence of Cancer-Associated Viral Infections in Healthy Afro-Caribbean Populations: A Review of the Literature

D. Heron, E. Taioli, S. Gollin, 2008, Cancer investigation.

TMEM16A induces MAPK and contributes directly to tumorigenesis and cancer progression.

Xin Huang, Dong Xiao, Umamaheswar Duvvuri, 2012, Cancer research.

Distinct distribution of HPV types among cancer-free Afro-Caribbean women from Tobago

C. Bunker, E. Taioli, S. Gollin, 2007, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

An abnormal clone with monosomy 7 and trisomy 21 in the bone marrow of a child with congenital agranulocytosis (Kostmann disease) treated with granulocyte colony-stimulating factor. Evolution towards myelodysplastic syndrome and acute basophilic leukemia.

S. Gollin, N. Wald, L. Penchansky, 1995, Cancer genetics and cytogenetics.

Rapid cell culture procedure for tissue samples.

S. Gollin, B. Gray, 1987, American journal of medical genetics.

Recurrence in oral and pharyngeal cancer is associated with quantitative MGMT promoter methylation

Scott M Langevin, E. Taioli, S. Gollin, 2009, BMC Cancer.

A stochastic model for cancer stem cell origin in metastatic colon cancer.

D. Stolz, S. Gollin, D. Geller, 2008, Cancer research.

Clonal chromosomal aberrations in a leiomyosarcoma of the sinonasal tract.

S. Gollin, L. Barnes, I. Janecka, 1993, Cancer genetics and cytogenetics.

Chemosensitization of head and neck cancer cells by PUMA

Jian Yu, J. Yu, S. Gollin, 2007, Molecular Cancer Therapeutics.

Upregulation of the ATR‐CHEK1 pathway in oral squamous cell carcinomas

J. Bauman, L. Appleman, S. Gollin, 2014, Genes, chromosomes & cancer.

Loss of distal 11q is associated with DNA repair deficiency and reduced sensitivity to ionizing radiation in head and neck squamous cell carcinoma

M. Romkes, Jason S. White, C. Bakkenist, 2007, Genes, chromosomes & cancer.

A prolonged response to platinum‐based therapy in a patient with metastatic urothelial carcinoma harboring a single rearranged and truncated NF2 gene

R. Dhir, Siraj M. Ali, S. Gollin, 2018, Genes, chromosomes & cancer.

Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.

S. Gollin, J. Sawyer, J. Overhauser, 1992, American journal of medical genetics.

Longitudinal bone marrow evaluations for myelodysplasia in patients with myeloma before and after treatment with lenalidomide

S. Gollin, D. Normolle, M. Mapara, 2013, Leukemia & lymphoma.

A genome-edited β-cell model of Prader-Willi syndrome reveals chronic deficits in endoplasmic reticulum chaperones and insulin secretion

Simon C Watkins, J. Diedrich, J. Yates, 2021 .

Mapping and analysis of HPV16 integration sites in a head and neck cancer cell line

S. Gollin, C. Ragin, S. Reshmi, 2004, International journal of cancer.

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

M. James, G. Evans, W. Rubinstein, 1997, American journal of human genetics.

Consistent numerical chromosome aberrations in congenital fibrosarcoma.

S. Gollin, W. Swaney, E. Wiener, 1993, Cancer genetics and cytogenetics.

Medulloblastoma and glioblastoma multiforme in a patient with Turcot syndrome: a case report.

S. Gollin, A. L. Albright, M. R. Mclaughlin, 1998, Surgical neurology.

Gliosarcoma with chromosome abnormalities in a neonate exposed to heptachlor.

S. Gollin, C. Araoz, W. Chadduck, 1987, Neurosurgery.

Confirmation of autosomal dominant transmission of the DiGeorge malformation complex.

A. Burks, S. Gollin, J. Sawyer, 1988, The Journal of pediatrics.

Deletion 6q is not a characteristic marker of nodal lymphoplasmacytic lymphoma.

Xin Huang, Shalini Reshmi, S. Swerdlow, 2005, Cancer genetics and cytogenetics.

Epidemiology of HPV-Associated Oropharyngeal Squamous Cell Carcinoma

S. Gollin, 2015 .

Overexpression of Cdc20 leads to impairment of the spindle assembly checkpoint and aneuploidization in oral cancer.

Shiladitya Sengupta, Susanta Roychoudhury, Shiladitya Sengupta, 2007, Carcinogenesis.

Polymorphisms in DNA damage response genes and head and neck cancer risk

S. Gollin, C. Ragin, R. Flores-Obando, 2010, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

Human papillomavirus-16 associated squamous cell carcinoma of the head and neck (SCCHN): a natural disease model provides insights into viral carcinogenesis.

R. Ferris, S. Gollin, S. Khan, 2005, European journal of cancer.

Roberts syndrome with normal cell division.

S. Gollin, J. Seibert, J. Sisken, 1991, American journal of medical genetics.

Lack of PAX5 rearrangements in lymphoplasmacytic lymphomas: reassessing the reported association with t(9;14).

S. Swerdlow, S. Gollin, Xin Huang, 2004, Human pathology.

Sheddase Activity of Tumor Necrosis Factor-α Converting Enzyme Is Increased and Prognostically Valuable in Head and Neck Cancer

R. Ferris, T. Whiteside, J. Hunt, 2009, Cancer Epidemiology, Biomarkers & Prevention.

Cigarette smoke induces anaphase bridges and genomic imbalances in normal cells.

S. Gollin, W. Saunders, Li Z. Luo, 2004, Mutation research.

Identification, expansion and characterization of cancer cells with stem cell properties from head and neck squamous cell carcinomas.

S. Gollin, Hatem O. Kaseb, E. Lagasse, 2016, Experimental cell research.

Loss of DNA Polymerase ζ Causes Chromosomal Instability in Mammalian Cells

R. Wood, S. Gollin, S. Reshmi, 2006 .

Loss of DNA polymerase zeta causes chromosomal instability in mammalian cells.

R. Wood, S. Gollin, S. Reshmi, 2006, Cancer research.

Malignancy after retinoblastoma: secondary cancer or recurrence?

S. Gollin, P. Dickman, J. Blatt, 1997, Human Pathology.

11q13 amplification status and human papillomavirus in relation to p16 expression defines two distinct etiologies of head and neck tumours

J. Weissfeld, E. Taioli, Jason S. White, 2006, British Journal of Cancer.

Studies of fs(1)1621, a mutation producing ovarian tumors in Drosophila melanogaster

S. Gollin, R. King, 1981 .

Concerning consequences of blocking Notch signaling in satellite muscle stem cells

S. Gollin, Hatem O. Kaseb, 2015, Front. Cell Dev. Biol..

Comparisons of high-risk cervical HPV infections in Caribbean and US populations

C. Bunker, E. Taioli, S. Gollin, 2009, Infectious Agents and Cancer.

Deficiency in Myosin Light Chain Phosphorylation Causes Cytokinesis Failure and Multipolarity in Cancer Cells

S. Gollin, W. Saunders, Li Z. Luo, 2010, Oncogene.

Molecular and Cellular Pathobiology TMEM 16 A Induces MAPK and Contributes Directly to Tumorigenesis and Cancer Progression

A. Egloff, J. Grandis, B. Harfe, 2012 .

Detection and assignment of TP53 mutations in tumor DNA using peptide mass signature genotyping

J. Jarvik, S. Gollin, C. Telmer, 2003, Human mutation.

Flow cytometric detection of lymphocyte alterations in Huntington's disease.

I. Shoulson, S. Gollin, J. Leary, 1985, Life sciences.

Brief Communication Fra(1O)(q25): The BrdU Effect Is Substitution-Dependent

D. Ledbetter, G. Holmquist, S. Gollin, 2006 .

Relationship between FRA11F and 11q13 gene amplification in oral cancer

S. Gollin, W. Saunders, Xin Huang, 2007, Genes, chromosomes & cancer.

The Ultrastructural Organization of Prematurely Condensed Chromosomes

S. Hanks, W. Hittelman, S. Gollin, 1984, Journal of Cell Science.

Cell Culture Contamination

S. Gollin, Dale W. Lewis, 2017 .

Chromosomal instability and cytoskeletal defects in oral cancer cells.

I. Petersen, S. Gollin, W. Saunders, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Chromosomal Instability in Oral Cancer Cells

S. Gollin, S. Reshmi, S. Gollin, 2005, Journal of dental research.

FHIT gene alterations in head and neck squamous cell carcinomas.

C. Croce, K. Huebner, S. Gollin, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Cytogenetic alterations and their molecular genetic correlates in head and neck squamous cell carcinoma: A next generation window to the biology of disease

S. Gollin, Susanne M. Gollin, 2014, Genes, chromosomes & cancer.

Tumor escape from immune recognition: lethal recurrent melanoma in a patient associated with downregulation of the peptide transporter protein TAP-1 and loss of expression of the immunodominant MART-1/Melan-A antigen.

J. Bryant, M. Lotze, S. Gollin, 1996, The Journal of clinical investigation.

Targeted inhibition of ATR or CHEK1 reverses radioresistance in oral squamous cell carcinoma cells with distal chromosome arm 11q loss

S. Gollin, W. Saunders, W. Gooding, 2014, Genes, chromosomes & cancer.

Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites

U. Surti, A. Parwani, S. Gollin, 2007, Diagnostic pathology.

Loss of heterozygosity of the short arm of chromosomes 3 and 9 in oral cancer

R. Ferrell, J. C. Law, S. Gollin, 1996, International journal of cancer.

Janet Davison Rowley, M.D. (1925–2013).

S. Gollin, S. Reshmi, 2014, American Journal of Human Genetics.

BASIC SCIENCE REVIEW

S. Gollin, Carl H. Snyderman, 2022 .

Longitudinal bone marrow evaluations for myelodysplasia in patients with myeloma before and after treatment with lenalidomide

S. Gollin, D. Normolle, M. Mapara, 2013, Leukemia and Lymphoma.

IMiD® Immunomodulatory Drugs Lenalidomide and Pomalidomide Inhibit the Maturation of Megakaryocytes by Suppressing the Expression of GATA1

D. Stolz, S. Gollin, V. Donnenberg, 2011 .

Chromosomal instability

S. Gollin, 2004, Current opinion in oncology.

The p53–PUMA axis suppresses iPSC generation

S. Gollin, T. Cheng, Shi-Yuan Cheng, 2013, Nature Communications.

Microsatellite instability in oral cancer

R. Ferrell, J. C. Law, S. Gollin, 1995, International journal of cancer.

The occurrence of chromosome segregational defects is an intrinsic and heritable property of oral squamous cell carcinoma cell lines.

S. Gollin, W. Saunders, J. Reing, 2004, Cancer genetics and cytogenetics.

Tumor escape from immune recognition: loss of HLA-A2 melanoma cell surface expression is associated with a complex rearrangement of the short arm of chromosome 6.

J. Karbach, M. Lotze, S. Gollin, 1996, Clinical cancer research : an official journal of the American Association for Cancer Research.