Dr. Donna G. Albertson

Dr. Donna G. Albertson's AcademicInfluence.com Rankings

Biology

#12568

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#16052

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Molecular Biology

#2055

World Rank

#2087

Historical Rank

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Biology

Dr. Donna G. Albertson's Degrees

PhD Molecular Biology Stanford University
Masters Biochemistry University of California, Berkeley
Bachelors Biology University of California, Berkeley

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Dr. Donna G. Albertson's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes. (2006) (3085)
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays (1998) (2340)
Genomic and transcriptional aberrations linked to breast cancer pathophysiologies. (2006) (1276)
Rac1b and reactive oxygen species mediate MMP-3-induced EMT and genomic instability (2005) (1231)
Fine-scale structural variation of the human genome (2005) (1081)
Assembly of microarrays for genome-wide measurement of DNA copy number (2001) (1019)
Segmental duplications and copy-number variation in the human genome. (2005) (946)
Chromosome aberrations in solid tumors (2003) (831)
A tiling resolution DNA microarray with complete coverage of the human genome (2004) (680)
The pharynx of Caenorhabditis elegans. (1976) (651)
Determinants of BRAF mutations in primary melanomas. (2003) (649)
Array comparative genomic hybridization and its applications in cancer (2005) (634)
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome (2006) (621)
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene (2000) (607)
The Caenorhabditis elegans male: postembryonic development of nongonadal structures. (1980) (566)
Gene amplification in cancer. (2006) (480)
Genomic microarrays in human genetic disease and cancer. (2003) (402)
Hidden Markov models approach to the analysis of array CGH data (2004) (393)
The Connectome of a Decision-Making Neural Network (2012) (379)
Fully automatic quantification of microarray image data. (2002) (367)
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome. (2006) (340)
Formation of the first cleavage spindle in nematode embryos. (1984) (314)
Breast tumor copy number aberration phenotypes and genomic instability (2006) (311)
DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly (2014) (300)
Rare amplicons implicate frequent deregulation of cell fate specification pathways in oral squamous cell carcinoma (2005) (287)
Production of antisense RNA leads to effective and specific inhibition of gene expression in C. elegans muscle. (1991) (280)
mec-7 is a beta-tubulin gene required for the production of 15-protofilament microtubules in Caenorhabditis elegans. (1989) (280)
Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors. (2003) (277)
Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH. (2003) (274)
Changes in Abundance of Oral Microbiota Associated with Oral Cancer (2014) (264)
DPY-27: A chromosome condensation protein homolog that regulates C. elegans dosage compensation through association with the X chromosome (1994) (256)
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas (2001) (248)
Piphillin: Improved Prediction of Metagenomic Content by Direct Inference from Human Microbiomes (2016) (247)
Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations. (2003) (247)
Genomic copy number analysis of non-small cell lung cancer using array comparative genomic hybridization: implications of the phosphatidylinositol 3-kinase pathway. (2002) (244)
Regional copy number–independent deregulation of transcription in cancer (2006) (242)
A Critical Role for FBXW8 and MAPK in Cyclin D1 Degradation and Cancer Cell Proliferation (2006) (198)
Segregation of holocentric chromosomes at meiosis in the nematode,Caenorhabditis elegans (1993) (197)
MALT1 is deregulated by both chromosomal translocation and amplification in B-cell non-Hodgkin lymphoma. (2003) (197)
Integrated genomic and epigenomic analyses pinpoint biallelic gene inactivation in tumors (2002) (183)
Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3 (2005) (157)
The use of chromosomal translocations to study human immunoglobulin gene organization: mapping DH segments within 35 kb of the C mu gene and identification of a new DH locus. (1988) (154)
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. (2002) (152)
Rac 1 b and reactive oxygen species mediate MMP-3-induced EMT and genomic instability (2009) (150)
Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization. (2003) (146)
Genomic Alterations in Primary Gastric Adenocarcinomas Correlate with Clinicopathological Characteristics and Survival (2004) (145)
Him-10 Is Required for Kinetochore Structure and Function on Caenorhabditis elegans Holocentric Chromosomes (2001) (135)
Genomic and Expression Analysis of the 8p11–12 Amplicon in Human Breast Cancer Cell Lines (2004) (135)
High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization. (2005) (134)
Genomic profiling of gastric cancer predicts lymph node status and survival (2003) (131)
A set of BAC clones spanning the human genome. (2004) (128)
Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors (2004) (121)
Profiling Breast Cancer by Array CGH (2003) (120)
Genome-wide array CGH analysis of murine neuroblastoma reveals distinct genomic aberrations which parallel those in human tumors. (2003) (116)
Co-amplified genes at 8p12 and 11q13 in breast tumors cooperate with two major pathways in oncogenesis (2009) (111)
Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high‐resolution microarray comparative genomic hybridization (2003) (110)
The kinetochores of Caenorhabditis elegans (2004) (106)
Sensitive and high resolution in situ hybridization to human chromosomes using biotin labelled probes: assignment of the human thymocyte CD1 antigen genes to chromosome 1. (1988) (101)
Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23–qter and identifies underlying candidate tumor suppressor genes in prostate cancer (2004) (98)
Chromosomal Instability in Microsatellite-Unstable and Stable Colon Cancer (2006) (97)
Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors. (2005) (95)
Shaping of tumor and drug-resistant genomes by instability and selection (2003) (85)
Deletion of chromosome 11q predicts response to anthracycline-based chemotherapy in early breast cancer. (2007) (85)
Identification of a candidate primary sex determination locus, fox-1, on the X chromosome of Caenorhabditis elegans. (1994) (85)
Cell cycling and DNA replication in a mutant blocked in cell division in the nematode Caenorhabditis elegans. (1978) (83)
High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays. (2003) (80)
Genomic organization of major sperm protein genes and pseudogenes in the nematode Caenorhabditis elegans. (1988) (80)
pRb Inactivation in Mammary Cells Reveals Common Mechanisms for Tumor Initiation and Progression in Divergent Epithelia (2004) (77)
Aging impacts transcriptomes but not genomes of hormone-dependent breast cancers (2007) (77)
Chromosome Organization, Mitosis, and Meiosis (1997) (76)
Array Comparative Genomic Hybridization Identifies Genetic Subgroups in Grade 4 Human Astrocytoma (2005) (74)
Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in Fallopian tube carcinoma (2003) (74)
Mapping muscle protein genes by in situ hybridization using biotin‐labeled probes. (1985) (74)
Mapping segmental and sequence variations among laboratory mice using BAC array CGH. (2005) (71)
Stromal-epithelial interactions in the progression of ovarian cancer: influence and source of tumor stromal cells (2001) (69)
Chromosome rearrangements in Caenorhabditis elegans. (1976) (68)
Localization of the ribosomal genes in Caenorhabditis elegans chromosomes by in situ hybridization using biotin‐labeled probes. (1984) (68)
Frequency and extent of allelic loss in the short arm of chromosome 3 in nonsmall‐cell lung cancer (1989) (67)
High‐resolution genomic profiling of occult micrometastatic tumor cells (2003) (65)
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22. (1991) (61)
Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome? (2002) (59)
Evaluation of genetic patterns in different tumor areas of intermediate‐grade prostatic adenocarcinomas by high‐resolution genomic array analysis (2004) (58)
Two Distinct Routes to Oral Cancer Differing in Genome Instability and Risk for Cervical Node Metastasis (2011) (56)
Therapy-induced malignant neoplasms in Nf1 mutant mice. (2005) (53)
A metastasis or a second independent cancer? Evaluating the clonal origin of tumors using array copy number data (2010) (49)
Comparison of gene expression and DNA copy number changes in a murine model of lung cancer (2006) (47)
Genomic organization of the glyceraldehyde-3-phosphate dehydrogenase gene family of Caenorhabditis elegans. (1989) (45)
Analysis of a T-cell tumor-specific breakpoint cluster at human chromosome 14q32. (1988) (45)
Specific keynote: genome copy number abnormalities in ovarian cancer. (2003) (44)
Fluorescence in situ hybridization for the detection of DNA and RNA. (1995) (42)
ErbB2 Activation of ESX gene expression (2002) (41)
Genomic organization of the 8p11-p12 amplicon in three breast cancer cell lines. (2004) (40)
Current status and future prospects of array-based comparative genomic hybridisation. (2003) (40)
Long-lived Min mice develop advanced intestinal cancers through a genetically conservative pathway. (2009) (39)
Network analysis of skin tumor progression identifies a rewired genetic architecture affecting inflammation and tumor susceptibility (2011) (39)
Centromeric chromosomal translocations show tissue-specific differences between squamous cell carcinomas and adenocarcinomas (2005) (35)
Conflicting evidence on the frequency of ESR1 amplification in breast cancer (2008) (32)
BAC microarray-based comparative genomic hybridization. (2004) (32)
Chromatin diminution and a chromosomal mechanism of sexual differentiation in Strongyloides papillosus (1979) (32)
APPENDIX 4 Genetics (1988) (32)
Genome position and gene amplification (2007) (32)
A novel calmodulin-like gene from the nematode Caenorhabditis elegans. (1986) (30)
Chromosomal instability and lack of cyclin E regulation in hCdc4 mutant human breast cancer cells (2004) (30)
Quantitation of Membrane Type Serine Protease 1 (MT-SP1) in Transformed and Normal Cells (2003) (26)
Xq chromosome duplication in males: Clinical, cytogenetic and array CGH characterization of a new case and review (2005) (26)
Neutrophil-Mediated Endogenous Analgesia Contributes to Sex Differences in Oral Cancer Pain (2018) (25)
Cooperativity of Rb, Brca1, and p53 in Malignant Breast Cancer Evolution (2012) (24)
Evidence of Convergent Evolution in Humans and Macaques Supports an Adaptive Role for Copy Number Variation of the β-Defensin-2 Gene (2014) (23)
Genomic Profiling by Array Comparative Genomic Hybridization Reveals Novel DNA Copy Number Changes in Breast Phyllodes Tumours (2008) (23)
The C. elegans expression pattern database: a beginning. (1996) (22)
Expression patterns of predicted genes from the C. elegans genome sequence visualized by FISH in whole organisms (1995) (22)
Acquired genomic aberrations associated with methotrexate resistance vary with background genomic instability (2008) (21)
Stromal control of oncogenic traits expressed in response to overexpression of GLI2, a pleiotropic oncogene (2008) (20)
Construction and application of a full‐coverage, high‐resolution, human chromosome 8q genomic microarray for comparative genomic hybridization (2005) (19)
Isolation of dominant XO-feminizing mutations in Caenorhabditis elegans: new regulatory tra alleles and an X chromosome duplication with implications for primary sex determination. (1995) (19)
The BAC Resource: Tools for Array CGH and FISH (2005) (19)
Investigation of HOXA9 promoter methylation as a biomarker to distinguish oral cancer patients at low risk of neck metastasis (2014) (18)
Deletion of Chromosome 11 q Predicts Response to Anthracycline-Based Chemotherapy in Early Breast Cancer (2007) (18)
Multicolour fluorescence in situ hybridisation to order small, single-copy probes on metaphase chromosomes. (1994) (17)
Interstitial deletion of chromosome 12q: Genotype–phenotype correlation of two patients utilizing array comparative genomic hybridization (2005) (17)
Ring 21 chromosome and a satellited 1p in the same patient: Novel origin for an ectopic NOR (2003) (16)
Comparative genomic hybridization. (2005) (16)
Molecular analysis of functional and nonfunctional genes for human ferrochelatase: isolation and characterization of a FECH pseudogene and its sublocalization on chromosome 3. (1994) (15)
Mapping chromosome rearrangement breakpoints to the physical map of Caenorhabditis elegans by fluorescent in situ hybridization. (1993) (14)
Mapping nonisotopically labeled DNA probes to human chromosome bands by confocal microscopy. (1991) (14)
Oncogenes overexpressed in metastatic oral cancers from patients with pain: potential pain mediators released in exosomes (2020) (13)
Duplication of distal 20q: clinical, cytogenetic and array CGH Characterization of a new case (2006) (12)
Peripheral nerve injury and sensitization underlie pain associated with oral cancer perineural invasion. (2020) (11)
Ordering of six polymorphic dna markers important in the delineation of 3p deletions in neoplasia (1992) (11)
Altered promoter usage characterizes monoallelic transcription arising with ERBB2 amplification in human breast cancers (2006) (10)
Loss of Blm enhances basal cell carcinoma and rhabdomyosarcoma tumorigenesis in Ptch1+/- mice. (2010) (10)
cec-1, a soma-specific chromobox-containing gene in C. elegans. (1996) (10)
Genomic profling of gastric cancer predicts lymph node status and survival (2003) (10)
ESR1 amplification in breast cancer: controversy resolved? (2012) (10)
Wavelet transforms for the analysis of microarray experiments (2003) (9)
The compatibility of compositional and structural features of aluminous large pore zeolites with sorption characteristics (2001) (9)
Abstract 4885: Changes in abundance of oral microbiota associated with oral cancer (2014) (8)
Genomic analysis of tumors by array comparative genomic hybridization: more is better. (2006) (8)
Detection of single clone deletions using array CGH: Identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system (2007) (8)
RFLP and mapping of human MOX-1 gene on chromosome 3. (1988) (8)
In situ hybridization using biotin-labeled probes. (1989) (7)
FBXW7 and DNA copy number instability (2008) (7)
Abstract 5473: Integrative approach towards the functionality of CIAO1 gene (2012) (7)
The Histopathology of Oral Cancer Pain in a Mouse Model and a Human Cohort (2020) (6)
Localization of polymorphic DNA probes frequently deleted in lung carcinoma (1989) (6)
High-efficiency microarray printer using fused-silica capillary tube printing pins. (2008) (4)
Statistical issues in the analysis of the array CGH data (2003) (4)
Microarray comparative genomic hybridization reveals a narrow gain at 20q13 in human gastric carcinomas (2001) (3)
Chromosome organization, mitosis, meiosis (1997) (3)
The use of double colour plasmid fluorescence in situ hybridisation to order markers for nine polymorphic loci on 3p (1991) (3)
DEfiNING PATHOLOGIC AND MOLECULAR CHARACTERISTICS OF TONGUE LESIONS IN THE 4NQO MOUSE CARCINOGENESIS MODEL (2019) (2)
Comparative genomic hybridization to microarrays as a means to study copy number variation in human disease (2002) (2)
Fluorescent in situ hybridization for the detection of DNA and RNA (1995) (2)
O39 Rare narrow amplicons in oral cancers and pre-cancers (2007) (2)
Erratum: Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas (Journal of Vascular Technology (2001) 29 (459-464)) (2001) (2)
Technical approaches for efficient high-precision nucleic acid analysis using DNA microarrays (2002) (2)
Mutations in TP53 and associated genomic abnormalities are dependent on breast cancer estrogen receptor status and patient age (2007) (2)
Human cancer genetics (2006) (2)
Gene mapping with the confocal microscope (1992) (1)
Genome copy number abnormalities in ovarian cancer (2003) (1)
High density array fabrication and readout method for a fiber optic biosensor (1998) (1)
High-resolution assessment of DNA loss in RIP-Tag mouse pancreatic carcinomas using comparative genomic hybridization to microarrays (1999) (1)
Whole genome scanning strongly predicts clinical outcome in differently treated subgroups of patients with lymph-node negative breast cancer (2005) (1)
Comparative genomic hybridzation using BAC genomic microarrays (2002) (1)
Comparative genomic hybridization to arrayed DNA targets (CGHa) for high resolution analysis of DNA sequence copy number changes (1997) (1)
Design of a Wide Field High Sensitivity Imaging System for Quantitative Analysis of CGHA Micro-Arrays. (1997) (1)
Molecular Genetics Methods in Discovery of Chromosome Structure (2015) (1)
Investigation of HOXA9 promoter methylation as a biomarker to distinguish oral cancer patients at low risk of neck metastasis (2014) (1)
Oral Cancer Cells Release Vesicles that Cause Pain (2022) (1)
111) Epidermal growth factor receptor signaling in oral cancer pain (2017) (1)
Comparative Genomic Hybridization (CGH)—Detection of Unbalanced Genetic Aberrations Using Conventional and Micro‐Array Techniques (2001) (1)
Genomic DNA Copy Number Alterations in Mouse Cancer Models and Human Cancer (2012) (1)
2078 (2017) (0)
Preparation of BAC DNA for microarry-based comparative genomic hybridization (2002) (0)
CHROMOSOME REARRANGEMENTS IN CAENORHABDZTZS ELEGANS (2003) (0)
Measurement of DNA sequence copy number variation using comparative genomic hybridization to microarrays (1999) (0)
Genome-wide Measurement of DNA Copy Number on BAC Microarrays (2016) (0)
Array comparative genomic hybridization and expression analyses for the identification of candidate oncogenes co-amplified on chromosomes 8p and 11q in breast cancer (2006) (0)
2078: NGF and TNF-α contribute to oral cancer pain by regulating pro-inflammatory cytokines (2017) (0)
Abnormal distribution of rDNA genes in cell line K562 — an in situ hybridisation study using biotin labelling (1989) (0)
Cell Type-Specific mRNA Amplification and Expression Profiling from Breast Tumor Sections (1998) (0)
Abstract 3426: A novel approach to copy number assessment by whole genome sequencing reveals extensive spatial heterogeneity in diffuse low-grade glioma (2014) (0)
Oral cancer patients experience mechanical and chemical sensitivity at the site of the cancer (2022) (0)
Abstract 52: QDNAseq: A bioinformatics pipeline for DNA copy number analysis from shallow whole genome sequencing with noise levels near the probabilistic lower limit imposed by read counting (2016) (0)
EVALUATION OF THE ROLE OF ORAL MICROBES IN THE PROMOTION OF CANCER IN A MOUSE CARCINOGENESIS MODEL (2017) (0)
Comparing the properties of human umbilical cord- derived mesenchymal stromal cells from preterm Versus full-term infants (2018) (0)
Genomic andtranscriptional aberrations linked tobreastcancer pathophysiologies (2006) (0)
Abstract 2774: Pain signals oral cavity cancer metastasis (2019) (0)
Abstract 2003: Detecting clonal relationships of multifocal tumors (2010) (0)
123 RFLP analysis of 44 non small cell lung tumor patients informative for allelic loss suggests the deletions on 3p are often very large (1989) (0)
Molecular Genetics of human Ferrochelatase in Erythropoietic Protoporphyria (1991) (0)
Abstract 2137: Association of copy number aberrations with oral cancer metastasis and progression of pre-malignant oral lesions (2010) (0)
Molecular Oncology: Comparative genomic hybridization (2013) (0)
O28: Genome position effects on gene amplification (2005) (0)
Genomic DNA microarray for comparative genomic hybridization (2006) (0)
Corrigendum: Regional copy number–independent deregulation of transcription in cancer (2008) (0)
Abstract 2133: Identification of driver genes for amplification of the narrow amplicon at 2q11 present in oral cancers and pre-cancers (2010) (0)
Impact of aging on genomic abnormalities in breast cancer (2005) (0)
Current status and future prospects of array-based comparative genomic (2003) (0)
Evaluation of oral cancer-induced chemosensitivity (2022) (0)
Corrigendum to Hidden Markov models approach to the analysis of array CGH data (2005) (0)
Abstract 6448: Oral cancer pain mediators released in exosomes are oncogenes with potential to shape the microenvironment and induce neuronal sensitivity (2020) (0)
O106. Profiling of metastatic and non-metastatic oral squamous cell carcinoma using array comparative genomic hybridization (2009) (0)
Title Network analysis of skin tumor progression identifies a rewired genetic architecture affecting inflammation and tumor susceptibility Permalink (2011) (0)
A Metastasis or a Second Independent Cancer ? Evaluating the Clonal Origin of Tumors Using Array-CGH Data (2017) (0)
Growth factors and genetic modifiers in vascular biology and cancer Program : Developmental and Stem Cell Biology (2017) (0)
Acollectionofbreastcancercelllinesforthestudyoffunctionally distinct cancer subtypes (2006) (0)
Comparative Genomic Hybridization in the Study of Human Disease (2006) (0)
Abstract 5079: A genomic copy number biomarker to identify oral cancer patients at low risk for metastasis (2012) (0)

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