Michael Dean

Q: What Schools Are Affiliated With Michael Dean

Michael Dean is affiliated with the following schools: University of California, Berkeley, California Institute of Technology, University of Regensburg, Stanford University, Baylor College of Medicine, Johns Hopkins University, Thomas Jefferson University, Kyoto University, University of Utah, Harvard University, University of Alabama at Birmingham

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Michael Dean

Engineering

#2522

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#3454

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Electrical Engineering

#463

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#516

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engineering Degrees

Michael Dean

Computer Science

#3484

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#3656

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Computational Linguistics

#186

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#190

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Machine Learning

#421

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#427

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Artificial Intelligence

#620

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#631

Historical Rank

computer-science Degrees

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Engineering
Computer Science

Michael Dean's Degrees

PhD Computer Science Stanford University
Masters Electrical Engineering University of California, Berkeley
Bachelors Computer Engineering University of California, Berkeley

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Michael Dean'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

The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function (2003) (3651)
Tumour stem cells and drug resistance (2005) (3551)
Identification of the cystic fibrosis gene: chromosome walking and jumping. (1989) (3207)
Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the CKR5 Structural Gene (1996) (2691)
The human ATP-binding cassette (ABC) transporter superfamily. (2001) (2327)
Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome (1996) (1990)
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. (2005) (1986)
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas (1997) (1501)
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy (1997) (1331)
Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration (2006) (1089)
The Genome of the Sea Urchin Strongylocentrotus purpuratus (2006) (1056)
Contrasting genetic influence of CCR2 and CCR5 variants on HIV-1 infection and disease progression. Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SFCC), ALIVE Study. (1997) (963)
A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance. (1998) (837)
Molecular cloning of cDNAs which are highly overexpressed in mitoxantrone-resistant cells: demonstration of homology to ABC transport genes. (1999) (828)
Genetic restriction of AIDS pathogenesis by an SDF-1 chemokine gene variant. ALIVE Study, Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SFCC) (1998) (761)
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas (1996) (756)
Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption (2001) (688)
The human ATP-binding cassette (ABC) transporter superfamily. (2001) (660)
Cell-cycle control of c-myc but not c-ras expression is lost following chemical transformation (1984) (658)
Single-Cell Exome Sequencing Reveals Single-Nucleotide Mutation Characteristics of a Kidney Tumor (2012) (636)
ABCA3 gene mutations in newborns with fatal surfactant deficiency. (2004) (609)
ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport. (2000) (578)
Evolution of the ATP-binding cassette (ABC) transporter superfamily in vertebrates. (2005) (572)
Mutation of the Stargardt Disease Gene (ABCR) in Age-Related Macular Degeneration (1997) (568)
Mutational spectra of PTEN/MMAC1 gene: a tumor suppressor with lipid phosphatase activity. (1999) (546)
Germline mutations in the von Hippel–Lindau disease tumor suppressor gene: Correlations with phenotype (1995) (532)
Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis. (1992) (530)
Sequence of MET protooncogene cDNA has features characteristic of the tyrosine kinase family of growth-factor receptors. (1987) (520)
Mechanism of met oncogene activation (1986) (518)
Detectable clonal mosaicism and its relationship to aging and cancer (2012) (512)
Novel mutations of the MET proto-oncogene in papillary renal carcinomas (1999) (498)
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. (1998) (490)
Genetic acceleration of AIDS progression by a promoter variant of CCR5. (1998) (483)
Acquired mutations in the MXR/BCRP/ABCP gene alter substrate specificity in MXR/BCRP/ABCP-overexpressing cells. (2001) (438)
The multidrug resistance transporter ABCG2 (breast cancer resistance protein 1) effluxes Hoechst 33342 and is overexpressed in hematopoietic stem cells. (2002) (432)
A closely linked genetic marker for cystic fibrosis (1985) (423)
Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation (2013) (423)
ABCG2: a perspective. (2009) (422)
ABC Transporters, Drug Resistance, and Cancer Stem Cells (2009) (418)
Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR (1998) (409)
Detecting single base substitutions as heteroduplex polymorphisms. (1992) (385)
Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A) (1999) (380)
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. (1997) (354)
A novel germ line juxtamembrane Met mutation in human gastric cancer (2000) (340)
Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively. (2001) (337)
Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients (1990) (337)
Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database. (1996) (331)
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease. (1999) (307)
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33 (2008) (304)
Complete Characterization of the Human ABC Gene Family (2001) (298)
Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred. (1999) (278)
Multidrug Efflux Pumps and Cancer Stem Cells: Insights Into Multidrug Resistance and Therapeutic Development (2011) (276)
Population and pedigree studies reveal a lack of association between the dopamine D2 receptor gene and alcoholism. (1990) (276)
ABCA3 mutations associated with pediatric interstitial lung disease. (2005) (268)
Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16. (1992) (266)
The human met oncogene is related to the tyrosine kinase oncogenes (1985) (261)
Optimization of the single‐strand conformation polymorphism (SSCP) technique for detection of point mutations (1993) (259)
Evolution of ATP-binding cassette transporter genes. (1995) (259)
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse (2013) (257)
Targeted therapy for cancer stem cells: the patched pathway and ABC transporters (2007) (251)
Genetics of HIV-1 infection: chemokine receptor CCR5 polymorphism and its consequences. (1999) (244)
The chemical defensome: environmental sensing and response genes in the Strongylocentrotus purpuratus genome. (2006) (235)
Regulation of c-myc transcription and mRNA abundance by serum growth factors and cell contact. (1986) (232)
Homologues of the human multidrug resistance genes MRP and MDR contribute to heavy metal resistance in the soil nematode Caenorhabditis elegans. (1996) (224)
Identification, expression, and pharmacology of a Cys23-Ser23 substitution in the human 5-HT2c receptor gene (HTR2C). (1995) (223)
The B30.2(SPRY) Domain of the Retroviral Restriction Factor TRIM5α Exhibits Lineage-Specific Length and Sequence Variation in Primates (2005) (222)
A Mammalian patched Homolog Is Expressed in Target Tissues of sonic hedgehog and Maps to a Region Associated with Developmental Abnormalities (*) (1996) (221)
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. (2013) (212)
Genetic variants in AVPR1A linked to autism predict amygdala activation and personality traits in healthy humans (2009) (205)
Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene. (1994) (202)
Single-cell landscape of the ecosystem in early-relapse hepatocellular carcinoma (2020) (201)
Polymorphisms in multidrug resistance 1 (MDR1) gene are associated with refractory Crohn disease and ulcerative colitis (2004) (192)
HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis (2017) (183)
Influence of the CCR2-V64I Polymorphism on Human Immunodeficiency Virus Type 1 Coreceptor Activity and on Chemokine Receptor Function of CCR2b, CCR3, CCR5, and CXCR4 (1998) (174)
Balanced polymorphism selected by genetic versus infectious human disease. (2003) (173)
The genetics of ATP-binding cassette transporters. (2005) (169)
ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia. (2012) (165)
Evolution of the vertebrate ABC gene family: analysis of gene birth and death. (2006) (158)
Novel alleles of the chemokine-receptor gene CCR5. (1997) (155)
Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer (2010) (154)
Extended haplotypes in the complement factor H (CFH) and CFH‐related (CFHR) family of genes protect against age‐related macular degeneration: Characterization, ethnic distribution and evolutionary implications (2006) (150)
Molecular Cloning of a Brain-specific, Developmentally Regulated Neuregulin 1 (NRG1) Isoform and Identification of a Functional Promoter Variant Associated with Schizophrenia*♦ (2007) (147)
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies (1999) (146)
The Essential Vertebrate ABCE1 Protein Interacts with Eukaryotic Initiation Factors* (2006) (145)
Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications. (2006) (144)
Two new genes from the human ATP-binding cassette transporter superfamily, ABCC11 and ABCC12, tandemly duplicated on chromosome 16q12. (2001) (140)
c-myc regulation during retinoic acid-induced differentiation of F9 cells is posttranscriptional and associated with growth arrest (1986) (139)
Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients. (1996) (138)
Tyrosine kinase oncogenes abrogate interleukin-3 dependence of murine myeloid cells through signaling pathways involving c-myc: conditional regulation of c-myc transcription by temperature-sensitive v-abl (1989) (134)
Analysis of the ABCA4 gene by next-generation sequencing. (2011) (134)
Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls. (2010) (131)
Evidence of association of APOE with age‐related macular degeneration ‐ a pooled analysis of 15 studies (2011) (130)
Induction of c-fos and c-myc mRNA by epidermal growth factor or calcium ionophore is cAMP dependent. (1986) (127)
The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial (1999) (126)
Single-Nucleotide Polymorphism (SNP) Analysis in the ABC Half-Transporter ABCG2 (MXR/BCRP/ABCP1) (2002) (125)
The ABC transporter gene family of Daphnia pulex (2009) (123)
A High-Throughput Cell-Based Assay for Inhibitors of ABCG2 Activity (2006) (122)
Comparison of variations detection between whole-genome amplification methods used in single-cell resequencing (2015) (121)
Surfactant Composition and Function in Patients with ABCA3 Mutations (2006) (120)
Single-cell transcriptomics reveals regulators underlying immune cell diversity and immune subtypes associated with prognosis in nasopharyngeal carcinoma (2020) (119)
Identification of a fourth half ABC transporter in the human peroxisomal membrane. (1997) (118)
Estrogen Receptor Genotypes and Haplotypes Associated with Breast Cancer Risk (2004) (117)
Mosaic loss of chromosome Y is associated with common variation near TCL1A (2016) (114)
CCR2 chemokine receptor and AIDS progression (1997) (112)
Effects of human TRIM5α polymorphisms on antiretroviral function and susceptibility to human immunodeficiency virus infection (2006) (112)
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility (2009) (107)
Mutational analysis of ABCG2: role of the GXXXG motif. (2004) (105)
Evolution of a cytoplasmic tripartite motif (TRIM) protein in cows that restricts retroviral infection. (2006) (105)
D2 dopamine receptor genotype and cerebrospinal fluid homovanillic acid, 5‐hydroxyindoleacetic acid and 3‐methoxy‐4‐hydroxyphenylglycol in alcoholics in Finland and the United States (1992) (102)
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. (2020) (101)
22q11 deletion syndrome in childhood onset schizophrenia: an update (2004) (100)
Single-cell sequencing analysis characterizes common and cell-lineage-specific mutations in a muscle-invasive bladder cancer (2012) (100)
Structural and functional diversity calls for a new classification of ABC transporters (2020) (100)
Amplification of 4q21–q22 and the MXR gene in independently derived mitoxantrone‐resistant cell lines (2000) (99)
The genome of Diuraphis noxia, a global aphid pest of small grains (2015) (95)
A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults. (2014) (95)
Concurrent Alterations in TERT, KDM6A, and the BRCA Pathway in Bladder Cancer (2014) (94)
Mapping of the serotonin 5-HT1D beta autoreceptor gene on chromosome 6 and direct analysis for sequence variants. (1995) (94)
Specific regulation of c-myc oncogene expression in a murine B-cell lymphoma. (1984) (94)
Multilocus analysis of age-related macular degeneration (2009) (94)
HIV-1 Infection in Individuals With the CCR5-Δ32/Δ32 Genotype: Acquisition of Syncytium-Inducing Virus at Seroconversion (2002) (94)
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. (2011) (93)
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease. (2000) (92)
Polymorphic admixture typing in human ethnic populations. (1994) (91)
Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
Reduced risk of AIDS lymphoma in individuals heterozygous for the CCR5-delta32 mutation. (1999) (90)
Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes (2007) (88)
A frame-shift mutation in the cystic fibrosis gene (1990) (88)
Evolution of ABC transporters by gene duplication and their role in human disease (2011) (88)
Approaches to identify genes for complex human diseases: Lessons from Mendelian disorders (2003) (88)
Polymorphisms of the human IFNG gene noncoding regions (2000) (86)
Monocyte-derived neutrophil chemotactic factor (MDNCF/IL-8) resides in a gene cluster along with several other members of the platelet factor 4 gene superfamily (2004) (84)
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification (2019) (82)
Typing of HLA-DQA1 and DQB1 using DNA single-strand conformation polymorphism. (1992) (81)
Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism. (1992) (81)
In search of AIDS-resistance genes. (1997) (80)
The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing (2013) (78)
Organization of the ABCR gene: analysis of promoter and splice junction sequences. (1998) (76)
Molecular analysis of urothelial cancer cell lines for modeling tumor biology and drug response (2016) (73)
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (2016) (72)
Mutations in the human ATP‐binding cassette transporters ABCG5 and ABCG8 in sitosterolemia (2002) (72)
Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients. (1996) (71)
Naturally Occurring CCR5 Extracellular and Transmembrane Domain Variants Affect HIV-1 Co-receptor and Ligand Binding Function* (1999) (69)
Comparative genome analysis of potential regulatory elements in the ABCG5-ABCG8 gene cluster. (2002) (67)
Unique features of TRIM5α among closely related human TRIM family members (2007) (67)
XIIXVI. Yeast sequencing reports. Mapping and sequencing of two yeast genes belonging to the ATP‐binding cassette superfamily (1994) (67)
Cancer stem cells: redefining the paradigm of cancer treatment strategies. (2006) (67)
Identification and characterization of a novel ABCA subfamily member, ABCA12, located in the lamellar ichthyosis region on 2q34 (2003) (67)
Role of myc in the abrogation of IL3 dependence of myeloid FDC-P1 cells. (1987) (67)
An exhaustive DNA micro-satellite map of the human genome using high performance computing. (2003) (66)
Effects of human TRIM5alpha polymorphisms on antiretroviral function and susceptibility to human immunodeficiency virus infection. (2006) (65)
The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration. (1999) (62)
Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene. (1988) (62)
The Intersection of HPV Epidemiology, Genomics and Mechanistic Studies of HPV-Mediated Carcinogenesis (2018) (62)
The human ATP‐binding cassette (ABC) transporter superfamily (2022) (61)
Transcriptional activation of immunoglobulin α heavy-chain genes by translocation of the c-myc oncogene (1983) (61)
Comparison of 1D and 2D NMR spectroscopy for metabolic profiling. (2008) (61)
Genome Analysis of Latin American Cervical Cancer: Frequent Activation of the PIK3CA Pathway (2015) (60)
DRD4 dopamine receptor genotype and CSF monoamine metabolites in Finnish alcoholics and controls. (1995) (60)
Long homopurine•homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region (2006) (59)
Somatic Alterations Contributing to Metastasis of a Castration‐Resistant Prostate Cancer (2013) (59)
CYP1A1 and GSTM1 polymorphisms in relation to lung cancer risk in Chinese women. (2004) (59)
Enzyme therapy in genetic diseases (1979) (58)
Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients (2001) (57)
UBIAD1 Mutation Alters a Mitochondrial Prenyltransferase to Cause Schnyder Corneal Dystrophy (2010) (57)
Material for Detection of an Infectious Retrovirus , XMRV , in Blood Cells of Patients with Chronic Fatigue Syndrome (2009) (57)
New inhibitors of ABCG2 identified by high-throughput screening (2007) (57)
Cloning and organization of the abc and mdl genes of Escherichia coli: relationship to eukaryotic multidrug resistance. (1993) (56)
HIV-1 infection in individuals with the CCR5-Delta32/Delta32 genotype: acquisition of syncytium-inducing virus at seroconversion. (2002) (56)
Preparation of high titer lambda phage lysates. (1987) (55)
Unique features of TRIM5alpha among closely related human TRIM family members. (2007) (55)
The UBIAD1 Prenyltransferase Links Menaquione‐4 Synthesis to Cholesterol Metabolic Enzymes (2013) (54)
SMUCKLER/TIM4 is a distinct member of TIM family expressed by stromal cells of secondary lymphoid tissues and associated with lymphotoxin signaling (2004) (53)
DHPLC screening of cystic fibrosis gene mutations (2002) (53)
Somatic Host Cell Alterations in HPV Carcinogenesis (2017) (53)
Microsomal epoxide hydrolase polymorphisms and risk for advanced colorectal adenoma. (2005) (52)
Detecting high-resolution polymorphisms in human coding loci by combining PCR and single-strand conformation polymorphism (SSCP) analysis. (1991) (52)
Full-length single-cell RNA-seq applied to a viral human cancer: applications to HPV expression and splicing analysis in HeLa S3 cells (2015) (52)
Characterization of the rearranged tpr-met oncogene breakpoint (1987) (52)
Applications of heteroduplex analysis for mutation detection in disease genes (1995) (52)
Partial retraction. Detection of an infectious retrovirus, XMRV, in blood cells of patients with chronic fatigue syndrome. (2011) (52)
A locally funded Puerto Rican parrot (Amazona vittata) genome sequencing project increases avian data and advances young researcher education (2012) (51)
Dissecting spatial heterogeneity and the immune-evasion mechanism of CTCs by single-cell RNA-seq in hepatocellular carcinoma (2021) (49)
Efficacy of fluorescence-based PCR-SSCP for detection of point mutations. (1993) (49)
Association of Aflatoxin and Gallbladder Cancer. (2017) (49)
Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations (1994) (49)
Cancer as a complex developmental disorder--nineteenth Cornelius P. Rhoads Memorial Award Lecture. (1998) (49)
Phenotypic Expressions of CCR5-Δ32/Δ32 Homozygosity (1999) (49)
Evolutionary analysis of a cluster of ATP-binding cassette (ABC) genes (2003) (49)
Risk for HIV-1 Infection Associated With a Common CXCL12 (SDF1) Polymorphism and CXCR4 Variation in an African Population (2005) (47)
Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter (2001) (47)
Isolation and chromosomal mapping of a novel ATP-binding cassette transporter conserved in mouse and human. (1997) (47)
Allellic variants in regulatory regions of cyclooxygenase-2: association with advanced colorectal adenoma (2005) (47)
Human and mouse orthologs of a new ATP-binding cassette gene, ABCG4 (2002) (46)
Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3. (1995) (46)
Increased frequency of germline BRCA2 mutations associates with prostate cancer metastasis in a racially diverse patient population (2018) (45)
TET2 binds the androgen receptor and loss is associated with prostate cancer (2016) (45)
Genetic susceptibility in familial melanoma from northeastern Italy (2004) (45)
Effect of a 4-Month Tea Intervention on Oxidative DNA Damage among Heavy Smokers (2004) (44)
Cancer stem cells: Implications for cancer causation and therapy resistance. (2005) (43)
Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance (2020) (43)
Statistical estimation and pedigree analysis ofCCR2-CCR5 haplotypes (2001) (43)
The dMRP/CG6214 gene of Drosophila is evolutionarily and functionally related to the human multidrug resistance‐associated protein family (2004) (43)
Organization of the human T cell receptor zeta/eta gene and its genetic linkage to the Fc gamma RII-Fc gamma RIII gene cluster. (1992) (43)
Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis. (1988) (42)
What can we learn about age-related macular degeneration from other retinal diseases? (1999) (42)
Expression of 25 human ABC transporters in the yeast Pichia pastoris and characterization of the purified ABCC3 ATPase activity. (2007) (42)
Common germline MDR1/ABCB1 functional polymorphisms and haplotypes modify susceptibility to colorectal cancers with high microsatellite instability. (2008) (42)
Analysis of Mdr50: a Drosophila P-glycoprotein/multidrug resistance gene homolog. (1993) (41)
A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death. (1991) (41)
Variation and evolution of the ABC transporter genes ABCB1, ABCC1, ABCG2, ABCG5 and ABCG8: implication for pharmacogenetics and disease (2011) (41)
Structural analogues of smoothened intracellular loops as potent inhibitors of Hedgehog pathway and cancer cell growth. (2007) (41)
Genetic mapping of the beta 1 GABA receptor gene to human chromosome 4, using a tetranucleotide repeat polymorphism. (1991) (41)
Origins, admixture dynamics and homogenization of the African gene pool in the Americas (2019) (40)
The abcc6a gene expression is required for normal zebrafish development. (2010) (40)
Haplotype structure of inflammatory cytokines genes (IL1B, IL6 and TNF/LTA) in US Caucasians and African Americans (2004) (40)
Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2 (2015) (39)
An ATP-binding cassette gene (ABCG3) closely related to the multidrug transporter ABCG2 (MXR/ABCP) has an unusual ATP-binding domain (2001) (38)
The CEPH consortium linkage map of human chromosome 16. (1994) (38)
Tyramide signal amplification (TSA)-FISH applied to mapping PCR-labeled probes less than 1 kb in size. (1999) (38)
Conserved Intramolecular Disulfide Bond Is Critical to Trafficking and Fate of ATP-binding Cassette (ABC) Transporters ABCB6 and Sulfonylurea Receptor 1 (SUR1)/ABCC8* (2011) (37)
Mutational studies of G553 in TM5 of ABCG2: a residue potentially involved in dimerization. (2006) (36)
Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis. (1993) (35)
Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings. (2002) (35)
Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident (2021) (34)
Evolution of multiple cell clones over a 29-year period of a CLL patient (2016) (33)
Identification of 18 mouse ABC genes and characterization of the ABC superfamily in Mus musculus. (2000) (33)
Degeneration of an ATP-binding cassette transporter gene, ABCC13, in different mammalian lineages. (2004) (32)
The human ATP binding cassette gene ABCA13, located on chromosome 7p12.3, encodes a 5058 amino acid protein with an extracellular domain encoded in part by a 4.8-kb conserved exon (2003) (32)
A polymorphic dinucleotide repeat in the third intron of TAP1. (1994) (32)
Purification and ATP hydrolysis of the putative cholesterol transporters ABCG5 and ABCG8. (2006) (32)
Comparative molecular genetic profiles of anaplastic astrocytomas/ glioblastomas multiforme and their subsequent recurrences (1999) (32)
Geographic atrophy in age-related macular degeneration and TLR3. (2009) (31)
Retrospective family study of childhood medulloblastoma (2005) (31)
Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease (2007) (31)
Molecular and genetic analysis of cystic fibrosis. (1988) (30)
Differential Gene and MicroRNA Expression between Etoposide Resistant and Etoposide Sensitive MCF7 Breast Cancer Cell Lines (2012) (30)
A group of NotI jumping and linking clones cover 2.5 Mb in the 3p21-p22 region suspected to contain a tumor suppressor gene. (1995) (30)
Bringing age-related macular degeneration into focus (2008) (29)
An ATP-binding cassette gene (ABCG5) from the ABCG (White) gene subfamily maps to human chromosome 2p21 in the region of the Sitosterolemia locus (2001) (29)
Further linkage data on cystic fibrosis: the Utah Study. (1986) (29)
Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis. (1987) (28)
LMTK3 confers chemo-resistance in breast cancer (2018) (28)
Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes (2004) (28)
Construction of representative NotI linking libraries specific for the total human genome and for human chromosome 3. (1994) (28)
Arginine 383 is a crucial residue in ABCG2 biogenesis. (2009) (27)
The Distribution of High-Risk Human Papillomaviruses Is Different in Young and Old Patients with Cervical Cancer (2014) (27)
Molecular Evolutionary Analysis of ABCB5: The Ancestral Gene Is a Full Transporter with Potentially Deleterious Single Nucleotide Polymorphisms (2011) (27)
Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts (2012) (27)
The 6q22.33 Locus and Breast Cancer Susceptibility (2009) (27)
Analysis of the transforming potential of the human homolog of mos (1986) (26)
A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene. (1991) (26)
Mapping of the serotonin 5-HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region. (1995) (26)
CXCR4 polymorphisms and HIV-1 pathogenesis. (1998) (26)
Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: Study design, methods and feasibility (2006) (25)
Genetics and genomics of prostate cancer. (2013) (24)
Alternative splicing in the first nucleotide binding fold of CFTR. (1993) (24)
Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8. (1989) (24)
Approaches to localizing disease genes as applied to cystic fibrosis. (1990) (23)
A new mutation (1078delT) in exon 7 of the CFTR gene in a southern French adult with cystic fibrosis. (1992) (23)
The livestock photosensitizer, phytoporphyrin (phylloerythrin), is a substrate of the ATP-binding cassette transporter ABCG2. (2006) (23)
The ERCC6 Gene and Age-Related Macular Degeneration (2010) (23)
Polymorphisms in metalloproteinase-9 are associated with the risk for asthma in Mexican pediatric patients. (2013) (22)
The UBIAD1 Prenyltransferase Links Menaquinone‐4 Synthesis to Cholesterol Metabolic Enzymes (2013) (22)
Increased incidence and disparity of diagnosis of retinoblastoma patients in Guatemala. (2014) (22)
Next Generation Sequencing Reveals High Prevalence of BRCA1 and BRCA2 Variants of Unknown Significance in Early-Onset Breast Cancer in African American Women. (2017) (22)
Prevalence and spectrum of germline rare variants in BRCA1/2 and PALB2 among breast cancer cases in Sarawak, Malaysia (2017) (22)
Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: identification of six novel mutations. (2008) (22)
Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer (2009) (22)
Helpful hints for the detection of single-stranded conformation polymorphisms. (1991) (22)
Polarity, proliferation and the hedgehog pathway (1996) (22)
The genetic structure and adaptation of Andean highlanders and Amazonians are influenced by the interplay between geography and culture. (2020) (21)
Cloning of novel ABC transporter genes. (1998) (21)
Chromosomal localization of the met proto-oncogene in the mouse and cat genome. (1987) (21)
Research article - The genome of the sea urchin Strongylocentrotus purpuratus (2006) (21)
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls (2018) (20)
Comprehensive Analysis of Germline Variants in Mexican Patients with Hereditary Breast and Ovarian Cancer Susceptibility (2018) (20)
The SERPING1 gene and age-related macular degeneration (2008) (20)
ATP‐Binding Cassette (ABC) Transporters (2002) (20)
Identifying and characterizing a five‐gene cluster of ATP‐binding cassette transporters mapping to human chromosome 17q24: a new subgroup within the ABCA subfamily (2001) (20)
CCR5-Δ32 gene deletion in HIV-1 infected patients (1997) (20)
Analysis of the ABCA 4 Gene by Next-Generation Sequencing (2011) (20)
Three ATP-binding cassette transporter genes, Abca14, Abca15, and Abca16, form a cluster on mouse Chromosome 7F3 (2004) (19)
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers (2011) (19)
HPV self-sampling acceptability in rural and indigenous communities in Guatemala: a cross-sectional study (2019) (19)
Association assessment of copy number polymorphism and risk of age-related macular degeneration. (2011) (19)
Moving out: from sterol transport to drug resistance – the ABCG subfamily of efflux pumps (2011) (19)
Genetic signatures of gene flow and malaria-driven natural selection in sub-Saharan populations of the "endemic Burkitt Lymphoma belt" (2019) (19)
The use of DNA heteroduplex patterns to map recombination within the HLA class II region. (1991) (19)
Influence of the CCR 2V 64 I Polymorphism on Human Immunodeficiency Virus Type 1 Coreceptor Activity and on Chemokine Receptor Function of CCR 2 b , CCR 3 , CCR 5 , and CXCR 4 (1998) (19)
A Recurrent BRCA2 Mutation Explains the Majority of Hereditary Breast and Ovarian Cancer Syndrome Cases in Puerto Rico (2018) (19)
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022) (18)
Single‐stranded conformation polymorphism analysis of the CFTR gene in slovenian cystic fibrosis patients: Detection of mutations and sequence variations (1993) (18)
CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X. (1993) (18)
Screening for CF mutations in adult cystic fibrosis patients with a directed and optimized SSCP strategy (1994) (18)
PIK3Cδ expression by fibroblasts promotes triple-negative breast cancer progression. (2020) (17)
Molecular Cloning and Characterization of the Human ErbB4 Gene: Identification of Novel Splice Isoforms in the Developing and Adult Brain (2010) (17)
Allelic distribution of CCR5 and CCR2 genes in an Italian population sample. (2000) (17)
Cystic fibrosis patients from the black sea region: The 1677delTA mutation (1994) (17)
Resolving DNA mutations (1995) (17)
Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer (2010) (17)
Androgen receptor signaling regulates the transcriptome of prostate cancer cells by modulating global alternative splicing (2019) (17)
Use of denaturing HPLC to map human and murine genes and to validate single-nucleotide polymorphisms. (2000) (17)
Towards a unified model of tumor suppression: lessons learned from the human patched gene. (1997) (17)
Mosaic chromosome 20q deletions are more frequent in the aging population. (2017) (17)
Embryonic liver developmental trajectory revealed by single-cell RNA sequencing in the Foxa2eGFP mouse (2020) (16)
Polymorphisms in the 3′ untranslated region of the IκB/MAD-3 (NFKBI) gene located on chromosome 14 (1994) (15)
Genetics of the nevoid basal cell carcinoma syndrome. (1996) (15)
Human duplex sex determination PCR. (2001) (15)
Linkage mapping of the human CSF2 and IL3 genes. (1991) (14)
Common Genetic Variants and Modification of Penetrance of BRCA 2-Associated Breast Cancer (2010) (14)
Variants of CCR5, which are permissive for HIV-1 infection, show distinct functional responses to CCL3, CCL4 and CCL5 (2005) (14)
ABCC6 and Pseudoxanthoma Elasticum: The Face of a Rare Disease from Genetics to Advocacy (2017) (14)
The gene causing familial mediterranean fever maps to the short arm of chromosome 16 in Druze and Moslem Arab families (1994) (14)
The human chromogranin A gene: chromosome assignment and RFLP analysis. (1989) (14)
Contamination of cDNA- libraries and expressed-sequence-tags databases. (1995) (14)
Characterization of a class 3 tyrosine kinase. (1992) (14)
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia. (2020) (13)
Detection of an Infectious Retrovirus, XMRV, in Blood Cells of Patients with Chronic Fatigue Syndrome (2009) (13)
C to A single nucleotide polymorphism in intron 18 of the human MST1R (RON) gene that maps at 3p21.3. (2003) (13)
Partial Retraction (2011) (13)
Integrative molecular characterization of gallbladder cancer reveals microenvironment-associated subtypes. (2020) (13)
Phenotypic expressions of CCR5-delta32/delta32 homozygosity. (1999) (13)
Screening for cystic fibrosis mutations in Southern France: Identification of a frameshift mutation and two missense variations (1992) (12)
Metastatic and recurrent adrenocortical cancer is not defined by its genomic landscape (2020) (12)
Characterization and mapping of three new mammalian ATP-binding transporter genes from an EST database (1995) (12)
cDNA cloning and mapping of mouse pleckstrin (Plek), a gene upregulated in transformation-resistant cells. (2000) (12)
Identification of cystic fibrosis mutations. (1991) (11)
Whole‐exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data (2018) (11)
Determining the hybridization temperature for S1 nuclease mapping. (1987) (11)
Erratum: 3pK, a new mitogen-activated protein kinase-activated protein kinase located in the small cell lung cancer tumor suppressor gene region (Molecular and Cellular Biology 16:3 (868)) (1996) (11)
Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls (2015) (11)
CHAPTER 3 – HUMAN AND DROSOPHILA ABC PROTEINS (2003) (11)
Participants in HIV Study: Correction. (1996) (10)
Cystic fibrosis gene mutations detected in hereditary pancreatitis (2006) (10)
Frequency of thiopurine S-methyltransferase mutant alleles in indigenous and admixed Guatemalan patients with acute lymphoblastic leukemia (2013) (10)
The met oncogene: a new member of the tyrosine kinase family and a marker for cystic fibrosis. (1986) (10)
Aflatoxin B1 exposure and liver cirrhosis in Guatemala: a case–control study (2020) (10)
Regular ArticleThe CEPH Consortium Linkage Map of Human Chromosome 11 (1995) (9)
Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation (2004) (9)
Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens (2000) (9)
Low-cost HPV testing and the prevalence of cervical infection in asymptomatic populations in Guatemala (2017) (9)
A closely linked genetic marker for cystic fibrosis (1986) (9)
Assessment of a New Lower-Cost Real-Time PCR Assay for Detection of High-Risk Human Papillomavirus: Useful for Cervical Screening in Limited-Resource Settings? (2017) (9)
The Human TET2 Gene Contains Three Distinct Promoter Regions With Differing Tissue and Developmental Specificities (2019) (9)
Variants in ARID5B gene are associated with the development of acute lymphoblastic leukemia in Mexican children (2018) (9)
A rare null allele potentially encoding a dominant-negative TRIM5alpha protein in Baka pygmies. (2009) (9)
The genetic structure and adaptation of Andean highlanders and Amazonian dwellers is influenced by the interplay between geography and culture (2020) (8)
Tumor heterogeneity assessed by sequencing and fluorescence in situ hybridization (FISH) data (2020) (8)
Reply to ‘Mosaic loss of chromosome Y in leukocytes matters’ (2018) (8)
The Dopamine D2 Receptor Gene and Alcoholism-Reply (1991) (8)
Cystic fibrosis-related diabetes is associated with HLADQB1 alleles encoding Asp-57− molecules (1994) (8)
CCR5-delta 32 gene deletion in HIV-1 infected patients. (1997) (8)
ATM mutations and protein expression are not associated with familial B-CLL cases. (2003) (8)
Genomic DNA sequence of Rhesus (M. mulatta) cystic fibrosis (CFTR) gene (1998) (8)
Evidence that hereditary pancreatitis is genetically heterogeneous disorder (2000) (7)
Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel‐type zinc finger sequence on chromosome segment 9q22.3 (1997) (7)
Characterization of a new SNP c767A/T (Arg222Trp) in the candidate TSG FUS2 on human chromosome 3p21.3: prevalence in Asian populations and analysis of association with nasopharyngeal cancer. (2004) (7)
Metformin and Androgen Receptor-Axis-Targeted (ARAT) Agents Induce Two PARP-1-Dependent Cell Death Pathways in Androgen-Sensitive Human Prostate Cancer Cells (2021) (7)
New Nomenclature of Human ABC Transporter Genes (2000) (7)
The human met oncogene is a member of the tyrosine kinase family. (1986) (7)
Characterization of a human homolog (OVOL1) of the Drosophila ovo gene, which maps to Chromosome 11q13 (1997) (7)
A 22-bp deletion in the coding region of the cystic fibrosis gene. (1992) (7)
Abrogation of IL-3 dependence of myeloid FDC-P1 cells by tyrosine kinase oncogenes is associated with induction of c-myc. (1988) (7)
Using self-collection HPV testing to increase engagement in cervical cancer screening programs in rural Guatemala: a longitudinal analysis (2020) (6)
The ERCC 6 Gene and Age-related Macular Degeneration (2010) (6)
Linkage mapping of human polymorphic proteins identified by two-dimensional electrophoresis. (1991) (6)
New ABC transporters in multi-drug resistance (2000) (6)
Natural animal models of human genetic diseases. (2002) (6)
Identification of a rare cystic fibrosis mutation (S4X) in a Slovenian population. (1993) (6)
Identification of P-glycoprotein/multidrug resistance genes from model organisms. (1993) (6)
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. (2021) (6)
Comprehensive analysis of immune evasion in breast cancer by single-cell RNA-seq (2018) (6)
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration (2012) (5)
Two Novel Missense Mutations (R766M and R792G) in Exon 13 of the CFTR Gene in a Patient with Congenital Bilateral Absence of the Vas deferens (2000) (5)
Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer (2010) (5)
LMTK 3 confers chemo-resistance in breast cancer (2018) (5)
Genetic and Epigenetic Regulation of the Smoothened Gene (SMO) in Cancer Cells (2020) (5)
Genome diversity in Ukraine (2020) (5)
Cellular oncogenes, growth factors, and cellular growth control. (1984) (5)
CHRM2 but not CHRM1 or CHRM3 polymorphisms are associated with asthma susceptibility in Mexican patients (2014) (5)
Aflatoxin and the Etiology of Liver Cancer and Its Implications for Guatemala. (2021) (4)
Screening methods for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in non-human primates (2000) (4)
ABC Transport Genes in Mitoxantrone-resistant Cells : Demonstration of Homology Molecular Cloning of cDNAs Which Are Highly Overexpressed (1998) (4)
Description of Genetic Variants in BRCA Genes in Mexican Patients with Ovarian Cancer: A First Step towards Implementing Personalized Medicine (2018) (4)
Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia (1993) (4)
ATP-binding Cassette (ABC) Transporter Supergene Family: Genetics and Evolution (2006) (4)
The 6 q 22 . 33 Locus and Breast Cancer Susceptibility (2009) (4)
An oncogenic chromosome 8-9 gene fusion isolated following transfection of human ovarian carcinoma cell line DNA. (1990) (4)
Evidence that hereditary pancreatitis is genetically heterogeneous disorder (2000) (4)
T cell antigen receptor-eta subunit. Low levels of expression and limited cross-species conservation. (1993) (4)
Targeted Deep Sequencing of Bladder Tumors Reveals Novel Associations between Cancer Gene Mutations and Mutational Signatures with Major Risk Factors (2019) (4)
Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region. (1997) (4)
Extended Haplotypes in the Complement Factor H (CFH) and CFH- related (CFHR) Family of Genes that Protect against Age-related Macular Degeneration: Identification, Ethnic Distribution and Evolutionary Implications (2007) (3)
ABC transporters in the Daphnia pulex genome: Implications for ecotoxicology and drug resistance in crustacean parasites (2009) (3)
New inhibitors of ABCG 2 identified by high-throughput screening (2007) (3)
Characterization of Philadelphia-like Pre-B Acute Lymphoblastic Leukemia: Experiences in Mexican Pediatric Patients (2022) (3)
Biochemical and genetic analysis of a child with cystic fibrosis and cystinosis. (1991) (3)
The D2 and D3 Sublineages of Human Papilloma Virus 16–Positive Cervical Cancer in Guatemala Differ in Integration Rate and Age of Diagnosis (2020) (3)
Joint Clustering of Single-Cell Sequencing and Fluorescence In Situ Hybridization Data for Reconstructing Clonal Heterogeneity in Cancers (2021) (3)
scDPN for High-throughput Single-cell CNV Detection to Uncover Clonal Evolution During HCC Recurrence (2021) (3)
Germline variants in hereditary breast cancer genes are associated with early age at diagnosis and family history in Guatemalan breast cancer (2020) (3)
Spatially resolved gene regulatory and disease-related vulnerability map of the adult Macaque cortex (2022) (3)
Cancer Stem Cells: Similarities and Variations in the Theme of Normal Stem Cells (2008) (3)
Deregulation of the c-myc and N-myc genes in transformed cells. (1988) (3)
Screening methods for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in non-human primates (2000) (3)
Analysis of TP53 aflatoxin signature mutation in hepatocellular carcinomas from Guatemala: A cross‐sectional study (2016‐2017) (2020) (3)
Tracing the Distribution of European Lactase Persistence Genotypes Along the Americas (2021) (2)
Two Rare Confounding Polymorphisms Proximal to the Factor V Leiden Mutation (2001) (2)
Chromosomal localization of the human and murine orthologues of the Drosophila smoothened gene. (1998) (2)
Cervical Visual Inspection with Acetic Acid (VIA) and Oncogenic Human Papillomavirus Screening in Rural Indigenous Guatemalan Women: Time to Rethink VIA (2021) (2)
Extrachromosomal Amplification of Human Papillomavirus Episomes as a Mechanism of Cervical Carcinogenesis (2021) (2)
Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens. (2000) (2)
Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8 (1990) (2)
HPV16 E7 Nucleotide Variants Found in Cancer-Free Subjects Affect E7 Protein Expression and Transformation (2021) (2)
Activation of proto-oncogene expression by growth regulatory signals. (1986) (2)
Overproduction of immunoglobulin mRNA by a murine myeloma MOPC 315 variant cell line. (1984) (2)
The Human Genes that Limit AIDS (2000) (2)
Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error? (1993) (2)
Dinucleotide repeat and alu repeat polymorphisms at the 5-HT1A(HTR1 A) receptor gene (1993) (2)
Gene Panel Sequencing in a Chinese High-risk Breast Cancer Cohort (2019) (2)
C306A single nucleotide polymorphism in the human CEBPD gene that maps at 8p11.1-p11.2. (2001) (2)
Associations between aflatoxin B1 ‐albumin adduct levels with metabolic conditions in Guatemala: A cross‐sectional study (2022) (1)
Advances in Brief Reduced Risk of AIDS Lymphoma in Individuals Heterozygous for the CCR 5D 32 Mutation 1 (1999) (1)
A retrospective family study of childhood medulloblastoma (Am J Med Genet 134A(4): 399–403) (2005) (1)
Abstract 1294: Prevalence and spectrum of germline rare variants inBRCA1/2andPALB2among breast cancer cases in Sarawak, Malaysia (2017) (1)
Abstract 4783: Novel molecular markers of bladder cancer progression identified by global chromatin profiling (2015) (1)
What can we learn about AMD from other retinal diseases ? (1999) (1)
Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens (2000) (1)
Mosaic loss of chromosome Y is associated with common variation near TCL 1 A 1 2 (2016) (1)
hOGG1 Genotype, Green Tea and Oxidative DNA Damage among Heavy Smokers (2004) (1)
The D2 Dopamine Receptor Gene and CSF Homovanillic Acid. (1992) (1)
Linkage Analysis for Monogenic Traits (2010) (1)
Mapping of 22Notl linking clones on human chromosome 3 by polymerase chain reaction and somatic cell hybrid panels (2005) (1)
Abstract 1333: Specific RB1 mutations and risk of subsequent neoplasms among survivors of hereditary retinoblastoma. (2013) (1)
Combined somatic mutation and copy number analysis in the survival of familial CLL (2018) (1)
Biology of Human Tumors Concurrent Alterations in TERT , KDM 6 A , and the BRCA Pathway in Bladder Cancer (2014) (1)
Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2020) (1)
Single-cell regulatory landscape and disease vulnerability map of adult Macaque cortex (2020) (1)
High prevalence of precocious menarche in Puerto Barrios, Guatemala (2019) (1)
Syndrome Blood Cells of Patients with Chronic Fatigue Detection of an Infectious Retrovirus , XMRV (2010) (1)
Molecular analysis of northwestern Mexican patients with cystic fibrosis: screening of 10 known mutations. Mutations in brief no. 185. Online. (1998) (1)
Genetic markers for oncogenes, growth factors, and cystic fibrosis. (1989) (1)
Human papillomavirus 16 positive cervical cancer in Guatemala: The D2 and D3 sublineages differ in integration rate and age of diagnosis (2020) (1)
Cancer Stem Cells and New Therapeutic Approaches (2008) (1)
Diverse evolutionary dynamics in glioblastoma inference by multi-region and single-cell sequencing. (2016) (1)
Genome-Wide Association Study Identifies a Novel Susceptibility Locus At 10p12.31-12.2 for Childhood Acute Lymphoblastic Leukemia in Ethinically Diverse Populations (2012) (1)
Breast Cancer Stem Cells (2009) (1)
Spatially resolved gene regulatory and disease vulnerability map of the adult Macaque cortex (2022) (1)
Sequence Variant in the TRIM39-RPP21 Gene Readthrough is Shared Across a Cohort of Arabian Foals Diagnosed with Juvenile Idiopathic Epilepsy. (2022) (1)
Common Mechanisms of Virus-Mediated Oncogenesis in Bladder Cancers Arising In Solid Organ Transplant Recipients (2021) (1)
Immune regulation of the c-myc oncogene in a murine B lymphoma. (1984) (1)
Activation of the met proto-oncogene in a human cell line. (1987) (1)
Clinically Relevant Germline Mutations in a Cohort of Young Women with Breast Cancer: A Comprehensive Analysis of Hereditary-Cancer Genes from Whole-Exome Sequencing (2020) (1)
Use of genome-wide scan in women with breast cancer to identify common germline variants that may be associated with recurrence. (2009) (0)
Abstract 1240: Comprehensive analysis of germline variants in Mexican patients with hereditary breast and ovarian cancer susceptibility (2018) (0)
Mutated UBIAD1 in Schnyder Corneal Dystrophy Binds HMGCR and Vitamin K Biosynthesis Is Impaired (2012) (0)
Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2021) (0)
DNA markers for the cystic fibrosis locus. (1987) (0)
Inherited GATA3 genetic Variants Are Associated With Childhood BCR-ABL1-Like Acute Lymphoblastic Leukemia and Increased Risk Of Relapse (2013) (0)
Systematic Reviews and Meta- and Pooled Analyses Variations in Apolipoprotein E FrequencyWith Age in a Pooled Analysis of a Large Group of Older People (2011) (0)
Abstract 148: Analysis of the tumor microenvironment in seven cancer types by single-cell RNA-seq (2019) (0)
From Gene to Therapy: Understanding Human Disease through Genetics (2017) (0)
Exome sequencing of multiple metastases from a lethal prostate cancer reveals BRCA1 deficiency and additional somatic alterations which suggest alternate therapeutic options (2010) (0)
Abstract 4782: Genome-wide chromatin profiling in bladder and prostate cancers (2015) (0)
ATP‐Binding Cassette (ABC) Transporter Supergene Family: Genetics and Evolution (2006) (0)
Table 3, ABC genes: human and mouse orthologs (2002) (0)
Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts (2012) (0)
Identification of a new breast cacner risk locus in a genome-wide association study of Ashkenazi Jews (2008) (0)
Table 5, Drosophila ABC genes (2002) (0)
Abstract C121: Genomic characterization of invasive cervical cancer in Guatemala and Venezuela: Common activation of the PIK3CA pathway. (2013) (0)
HIV‐1 Infection in Individuals With the CCR5‐&dgr;32/&dgr;32 Genotype: Acquisition of Syncytium‐Inducing Virus at Seroconversion (2002) (0)
Discovery of A Novel UBIAD1 Mutation In A Swede Finn Pedigree With Schnyder Corneal Dystrophy Identified Two Decades Ago (2011) (0)
Aflatoxin levels and prevalence of TP53 aflatoxin-mutations in hepatocellular carcinomas in Mexico. (2022) (0)
Figure 5, Map of the Drosophila ABC genes (2002) (0)
Polymorphic Admixture TypinginHuman Ethnic Populations (1994) (0)
Characterizing the Emergence of Liver and Gallbladder from the Embryonic Endoderm through Single-Cell RNA-Seq (2019) (0)
Embryonic liver developmental trajectory revealed by single-cell RNA sequencing in the Foxa2eGFP mouse (2020) (0)
Correction to: Low-cost HPV testing and the prevalence of cervical infection in asymptomatic populations in Guatemala (2020) (0)
Screening methods for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in non-human primates. (2000) (0)
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022) (0)
Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia (2019) (0)
D7S449 detects a HindIII polymorphism tightly linked to the MET gene on chromosome 7. (1990) (0)
Low-cost HPV testing and the prevalence of cervical infection in asymptomatic populations in Guatemala (2018) (0)
Abstract 2198: Exome and transcriptome sequencing of human tumors and tumor-derived cell lines (2010) (0)
Elaborating the Tumor Ecosystem of Primary and Relapsed Hepatocellular Carcinoma by Single-Cell RNA Sequencing (2019) (0)
Correction to: Low-cost HPV testing and the prevalence of cervical infection in asymptomatic populations in Guatemala (2020) (0)
Correction to: Germline variants in hereditary breast cancer genes are associated with early age at diagnosis and family history in Guatemalan breast cancer (2021) (0)
Next GeNeratioN SequeNciNG revealS HiGH PrevaleNce (2017) (0)
United Kingdom: Implementation of EU Law (1995) (0)
Nationwide Study of Breast Cancer Risk Factors in Latinas (2011) (0)
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls (2018) (0)
Determination of Zearalenone in Urine Samples from Guatemala: A Pilot Assessment (2022) (0)
Analysis of TP53 gene mutations demonstrates that aflatoxin is a risk factor for hepatocellular carcinoma in Guatemala (2019) (0)
Figure 3, Phylogenetic tree of the human ABC genes (2002) (0)
Cancer: Blueprint of a Tumor (2018) (0)
OP-MOLB200033 1647..1656 (2020) (0)
Figure 2, ABC gene structure (2002) (0)
Abstract 1650: Deconvolution of copy number alterations combining bulk and single-cell genomic data (2019) (0)
The genome of Diuraphis noxia, a global aphid pest of small grains (2015) (0)
Genetics of Latin American Diversity (GLAD) Project: insights into population genetics and association studies in recently admixed groups in the Americas (2023) (0)
Abstract A69: Identification of prostate cancer genes in the African American Hereditary Prostate Cancer (AAHPC) study (2011) (0)
Abstract A52: Gene alterations associated with clinical characteristics of bladder cancer (2016) (0)
Author Correction: Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022) (0)
UvA-DARE ( Digital Academic Repository ) The ERCC 6 Gene and Age-Related Macular Degeneration (2010) (0)
Editorial: The Genetic Causes Underlying Immune Mediated Disease: A Focus on Autoimmunity and Cancer (2022) (0)
Genome-wide homozygosity and risk of four non-Hodgkin lymphoma subtypes (2021) (0)
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinsons Disease in African and African Admixed Populations (2023) (0)
High-throughput Single-cell CNV Detection Reveals Clonal Evolution During Hepatocellular Carcinoma Recurrence (2020) (0)
Abstract #5613: Functional analysis of the promoter of the beta-microseminoprotein gene MSMB demonstrates the importance of a single nucleotide polymorphism in prostate cancer susceptibility (2009) (0)
HLA-A*03 is a Predictive Biomarker of Poor Response to Immune Checkpoint Blockade in Cancer (2021) (0)
Table 2, Diseases and phenotypes caused by ABC genes (2002) (0)
Figure 4, Phylogenetic tree of the human and Drosophila G subfamily ABC genes (2002) (0)
Abstract 454:TET2alterations facilitate progression of metastatic prostate cancer (2014) (0)
Insights into eye diseases and biology using genetics (2014) (0)
Reply to ‘Mosaic loss of chromosome Y in leukocytes matters’ (2018) (0)
Table 6, ABC gene subfamilies in characterized eukaryotes (2002) (0)
Converging on Alzheimer Disease loci in chromosome 10 (2009) (0)
Strategies for Gene Discovery (2019) (0)
Sample collection for human genetics (2007) (0)
Lipoid proteinosis: a lysosomal storage disease? (1983) (0)
ABCR/Stargardt Disease (2002) (0)
Abstract 1105: Clinical associations between altered bladder cancer genes (2015) (0)
Sampling the Conformational Space of the Parkinson's Disease Associated Protein Alpha-Synuclen (2018) (0)
HLA-DQA and DQB allele frequencies in cystic fibrosis patients with insulin-dependent diabetes (IDDM) (1991) (0)
Abstract 861: Diesel engine exhaust is associated withTP53mutations and high-risk non-muscle invasive bladder cancer (2021) (0)
O-276 Diesel exhaust exposure and somatic mutations in bladder tumors (2021) (0)
Nitrated polycyclic aromatic hydrocarbon (nitro-PAH) signatures and somatic mutations in diesel exhaust-exposed bladder tumors. (2023) (0)
Evidence for virus-mediated oncogenesis in bladder cancers arising in solid organ transplant recipients. (2023) (0)
Abstract 1938: Germline mutations in breast cancer genes are associated with early age of diagnosis and triple negative disease in Guatemalan and US Hispanic women (2023) (0)
Abstract LB-051: Integrative, targeted deep sequencing of bladder tumors reveals novel associations between cancer gene mutations and mutational signatures with major risk factors (2019) (0)
In Search of AIDS-Resistance Genes A genetic trait that protects against AIDS has now been uncovered, and others are emerging. The findings open entirely new avenues for developing preventives and therapies (1997) (0)
Using Stem Cells To Repair The Brain And Spinal Cord (2002) (0)
Abstract 48: Characterization of Human Papillomavirus (HPV) Sequence and Integration and Analysis of Immune Response Genes for Application in Guatemalan Cervical Cancer (2021) (0)
Figure 6, Model of ABCG5 and ABCG8 dimers (2002) (0)
Ethical Decision Making (2007) (0)
Abstract A1-01: Translational genomics of urologic cancer genes (2015) (0)
Retinitis pigmentosa caused by a homozygous inactivating mutation in the Stargardt disease g ene ABCR (2012) (0)
Table 4, ABC transporters involved in drug resistance (2002) (0)
Abstract 4871: Whole-exome sequencing identifies a high frequency of germline deleterious variants in cancer predisposition genes in individuals with osteosarcoma (2017) (0)
Genomic Analysis of Etoposide Resistance Reveals Multiple Alterations of Gene and microRNA Expression (2011) (0)
REGULATION OF HEAVY CHAIN GENE EXPRESSION IN MOUSE MYELOMA MOPC 315 CELLS (1982) (0)
Abstract LB-157: Association of aflatoxin and gallbladder cancer in Shanghai (2017) (0)
Abstract LB-426: Potent inhibitors of RAS pathways that bind directly to Ras proteins (2012) (0)
Aberrant type I IFN pathway response to viral infection in chronic fatigue syndrome (CFS) (2009) (0)
Report of the second international workshop on human chromosome 5 mapping: consensus genetic map. (1992) (0)
Abstract 355: TET2-loss modifies androgen signaling in prostate cancer (2017) (0)
The Identification of Genes for Complex Genetic Diseases (2000) (0)
Novel Alleles oftheChemokine-Receptor GeneCCR5 (1997) (0)
Abstract 474: Changes in global chromatin landscape identify bladder cancer progression (2014) (0)
Global kinome silencing combined with 3D invasion screening of the tumor microenvironment identifies fibroblast-expressed PIK3Cδ involvement in triple-negative breast cancer progression (2019) (0)
Physical mapping of the Gorlin syndrome region on 9q22 by pulsed field gel electrophoresis (PFGE) and FISH (1994) (0)
Abstract LB-202: A novel neoepitope screening platform for generating effective and safe neoantigen-based vaccines and immunotherapeutics in a hepatocellular carcinoma model (2017) (0)
The abcc6a Gene is Required for Normal Zebrafish Development (2012) (0)
Figure 1, Diagram of a typical ABC transporter protein (2002) (0)
Genetic Analysis of Ion Transport (1992) (0)
Properties of the met oncogene. (1986) (0)
Evidence that hereditary pancreatitis is genetically heterogeneous disorder. (2000) (0)
Molecular Analysis ofChromosome9qDeletions inTwoGorlin Syndrome Patients (1996) (0)
Germline Mutations in Latin American Women With Breast Cancer (2020) (0)
Table 1, List of human ABC genes, chromosomal location, and function (2002) (0)
Characterization of the bidirectional activity of the human TET2 gene promoters (2020) (0)
The effects of α-lipoic acid on oxidative stress during pig oocyte maturation (2015) (0)
Box 1, ABC transporter superfamily web resources (2002) (0)
Abstract 3352: Genome-wide enhancer identify signature predictive of metastatic phenotypes in bladder cancers (2017) (0)
Participants in HIV Study: Correction (1996) (0)
Abstract 2160: Immune escape mutations in HLA Class I,B2MandCASP8genes shape tumor evolution (2020) (0)
[13] Comparison of the sensitivity of single-strand conformational polymorphism and heteroduplex methods (1995) (0)
Abstract 140: Comprehensive analysis of immune evasion in breast cancer by single-cell RNA-seq (2019) (0)

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