Anne M. Bowcock

Q: What Schools Are Affiliated With Anne M. Bowcock

Anne M. Bowcock is affiliated with the following schools: Washington University in St. Louis, University of California, Berkeley, Imperial College London, Icahn School of Medicine at Mount Sinai, Princeton University, Stanford University, Columbia University, University of the Witwatersrand, University of Texas Southwestern Medical Center

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Anne M. Bowcock

Biology

#9128

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#12296

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Evolutionary Biology

#209

World Rank

#230

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Genetics

#929

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#1025

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Molecular Biology

#1221

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#1247

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Biology

Anne M. Bowcock's Degrees

PhD Genetics University of California, Berkeley
Masters Biology Stanford University

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Anne M. Bowcock's Published Works

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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

High resolution of human evolutionary trees with polymorphic microsatellites (1994) (1843)
Pathogenesis and therapy of psoriasis (2007) (1634)
Genomewide Scan Reveals Association of Psoriasis with IL-23 and NF-κB Pathways (2008) (1070)
Frequent Mutation of BAP1 in Metastasizing Uveal Melanomas (2010) (1032)
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome. (2000) (953)
Identification of a RING protein that can interact in vivo with the BRCA1 gene product (1996) (750)
A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci (2008) (670)
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity (2012) (555)
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis (2009) (520)
Psoriasis pathophysiology: current concepts of pathogenesis (2005) (506)
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34 (2002) (487)
Getting under the skin: the immunogenetics of psoriasis (2005) (478)
The immunogenetics of Psoriasis: A comprehensive review. (2015) (421)
Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma (2013) (419)
The C-terminal (BRCT) Domains of BRCA1 Interact in Vivo with CtIP, a Protein Implicated in the CtBP Pathway of Transcriptional Repression* (1998) (411)
Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) (397)
Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. (1991) (370)
Nonlesional atopic dermatitis skin is characterized by broad terminal differentiation defects and variable immune abnormalities. (2011) (357)
PSORS2 is due to mutations in CARD14. (2012) (351)
Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis. (2012) (325)
Novel mechanisms of T-cell and dendritic cell activation revealed by profiling of psoriasis on the 63,100-element oligonucleotide array. (2003) (322)
Genome-wide association analysis identifies three psoriasis susceptibility loci (2010) (314)
Oncogenic mutations in GNAQ occur early in uveal melanoma. (2008) (313)
Association analyses identify six new psoriasis susceptibility loci in the Chinese population (2010) (307)
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis (2003) (297)
Psoriasis vulgaris: cutaneous lymphoid tissue supports T-cell activation and "Type 1" inflammatory gene expression. (2004) (289)
Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C. (2000) (277)
The genetics of psoriasis: a complex disorder of the skin and immune system. (1998) (266)
The genetics of psoriasis, psoriatic arthritis and atopic dermatitis. (2004) (266)
Insights into psoriasis and other inflammatory diseases from large-scale gene expression studies. (2001) (259)
Psoriasis genetics: breaking the barrier. (2010) (245)
Histone Deacetylase Inhibitors Induce Growth Arrest and Differentiation in Uveal Melanoma (2011) (243)
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. (2015) (240)
Broad defects in epidermal cornification in atopic dermatitis identified through genomic analysis. (2009) (236)
Deep sequencing of small RNAs from human skin reveals major alterations in the psoriasis miRNAome. (2011) (231)
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. (2012) (231)
Association mapping of disease loci, by use of a pooled DNA genomic screen. (1997) (228)
Differential contributions of BRCA1 and BRCA2 to early-onset breast cancer. (1997) (221)
Psoriasis: genetic associations and immune system changes (2007) (201)
Completing the map of human genetic variation (2007) (199)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. (1989) (198)
Fine Mapping Major Histocompatibility Complex Associations in Psoriasis and Its Clinical Subtypes (2014) (190)
Reversal of atopic dermatitis with narrow-band UVB phototherapy and biomarkers for therapeutic response. (2011) (188)
A gene for congenital generalized lipodystrophy maps to human chromosome 9q34. (1999) (187)
Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers. (1998) (183)
Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q (1992) (181)
Cell cycle-dependent colocalization of BARD1 and BRCA1 proteins in discrete nuclear domains. (1997) (180)
Driver Mutations in Uveal Melanoma: Associations With Gene Expression Profile and Patient Outcomes. (2016) (179)
Genomic analysis defines a cancer-specific gene expression signature for human squamous cell carcinoma and distinguishes malignant hyperproliferation from benign hyperplasia. (2006) (175)
The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. (1988) (168)
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. (1993) (167)
Multiple Loci within the Major Histocompatibility Complex Confer Risk of Psoriasis (2009) (158)
Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21–22 (1998) (156)
Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene. (2002) (149)
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility (2015) (149)
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study. (1986) (148)
Localization of Susceptibility to Familial Idiopathic Scoliosis (2000) (145)
Genetic instability in human ovarian cancer cell lines. (1994) (143)
New insights into the pathogenesis and genetics of psoriatic arthritis (2009) (139)
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation. (2008) (134)
A subset of methylated CpG sites differentiate psoriatic from normal skin (2011) (134)
Punctuated evolution of canonical genomic aberrations in uveal melanoma (2018) (133)
The genetics of psoriasis and autoimmunity. (2005) (133)
Loss of Heterozygosity of Chromosome 3 Detected with Single Nucleotide Polymorphisms Is Superior to Monosomy 3 for Predicting Metastasis in Uveal Melanoma (2007) (130)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (1991) (129)
BRCA1 and BRCA2 mRNA levels are coordinately elevated in human breast cancer cells in response to estrogen. (1996) (123)
BAP1 deficiency causes loss of melanocytic cell identity in uveal melanoma (2013) (122)
Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene. (2001) (121)
Structure and Characterization of the Human Tissue Inhibitor of Metalloproteinases-2 Gene* (1996) (120)
Genome-wide meta-analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL (2011) (120)
A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16 (2000) (118)
CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis. (2007) (117)
Interferon alpha-inducible protein 27 (IFI27) is upregulated in psoriatic skin and certain epithelial cancers. (2004) (114)
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. (2011) (113)
A Regulatory Role for 1-Acylglycerol-3-phosphate-O-acyltransferase 2 in Adipocyte Differentiation* (2006) (113)
Molecular cloning and characterization of the human CLOCK gene: expression in the suprachiasmatic nuclei. (1999) (113)
Inactivation of human SRBC, located within the 11p15.5-p15.4 tumor suppressor region, in breast and lung cancers. (2001) (107)
Direct genomic selection (2005) (104)
Activating killer cell immunoglobulin-like receptor gene KIR2DS1 is associated with psoriatic arthritis. (2005) (101)
Genome-wide scan reveals association of psoriasis with IL-23 and NFB pathways (2016) (93)
Human population expansion and microsatellite variation. (2000) (92)
Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility (2002) (92)
A Genetic Risk Score Combining Ten Psoriasis Risk Loci Improves Disease Prediction (2011) (88)
Genetics of psoriasis: the potential impact on new therapies. (2003) (88)
Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7. (1989) (88)
High-density genetic map of the BRCA1 region of chromosome 17q12-q21. (1993) (86)
Epigenetic reprogramming and aberrant expression of PRAME are associated with increased metastatic risk in Class 1 and Class 2 uveal melanomas (2016) (86)
Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22. (2009) (84)
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21. (1993) (84)
The International Psoriasis Genetics Study: assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairs. (2003) (84)
Report of the committee on human gene mapping by recombinant DNA techniques. (1988) (84)
Rapid detection and sequencing of alleles in the 3' flanking region of the interleukin-6 gene. (1989) (82)
Biology of advanced uveal melanoma and next steps for clinical therapeutics (2014) (79)
Eight closely linked loci place the Wilson disease locus within 13q14-q21. (1988) (77)
Genetic Linkage Localizes an Adolescent Idiopathic Scoliosis and Pectus Excavatum Gene to Chromosome 18 q (2009) (71)
Breast cancer : molecular genetics, pathogenesis, and therapeutics (1999) (70)
Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR (2005) (70)
Localization of a gene for familial recurrent arthritis. (2000) (68)
AKT Inhibitors Promote Cell Death in Cervical Cancer through Disruption of mTOR Signaling and Glucose Uptake (2014) (67)
Association of Cardiovascular and Metabolic Disease Genes with Psoriasis (2012) (67)
The serotonin receptor subtype 2 locusHTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14 (1990) (66)
A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents (2004) (65)
CARD14‐associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris (2018) (64)
Carriers of rare missense variants in IFIH1 are protected from psoriasis. (2010) (64)
Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety. (2003) (64)
Microsatellite polymorphism linkage map of human chromosome 13q. (1993) (63)
Psoriasis Patients Are Enriched for Genetic Variants That Protect against HIV-1 Disease (2012) (62)
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1. (1996) (61)
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. (1987) (59)
Disruption of sodium bicarbonate transporter SLC4A10 in a patient with complex partial epilepsy and mental retardation. (2008) (59)
Study of 47 DNA markers in five populations from four continents. (1987) (55)
SNTG1, the gene encoding γ1-syntrophin: a candidate gene for idiopathic scoliosis (2004) (54)
Psoriasis mutations disrupt CARD14 autoinhibition promoting BCL10-MALT1-dependent NF-κB activation. (2016) (54)
Peptidoglycan recognition proteins Pglyrp3 and Pglyrp4 are encoded from the epidermal differentiation complex and are candidate genes for the Psors4 locus on chromosome 1q21 (2006) (53)
CARD14 Expression in Dermal Endothelial Cells in Psoriasis (2014) (52)
Predictive testing for Wilson's disease using tightly linked and flanking DNA markers (1991) (52)
Evolution of modern humans: evidence from nuclear DNA polymorphisms. (1992) (51)
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites. (1993) (51)
Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21. (1997) (48)
Conservation of function and primary structure in the BRCA1-associated RING domain (BARD1) protein (1998) (43)
The study of variation in the human genome. (1991) (43)
Noncanonical microRNAs and endogenous siRNAs in normal and psoriatic human skin. (2013) (43)
Mutations in the Novel Protein PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions (IN10-2.005) (2012) (42)
Genomics: Guilt by association (2007) (42)
DNA markers and genetic variation in the human species. (1986) (41)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14) (1990) (41)
Genetic analysis of PSORS2 markers in a UK dataset supports the association between RAPTOR SNPs and familial psoriasis (2004) (40)
Psoriasis bench to bedside: genetics meets immunology. (2009) (40)
Paroxysmal kinesigenic dyskinesia and infantile convulsions. Clinical and linkage studies. 2000. (2001) (39)
The human cationic amino acid transporter (ATRC1): physical and genetic mapping to 13q12-q14. (1992) (38)
Combined PKC and MEK inhibition for treating metastatic uveal melanoma (2014) (34)
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer (2018) (33)
Wilson's disease in Israel: a genetic and epidemiological study (1990) (33)
CARD14 alterations in Tunisian patients with psoriasis and further characterization in European cohorts (2016) (33)
Fine mapping of eight psoriasis susceptibility loci (2014) (32)
The PLC/PRF/5 human hepatoma cell line. II. Chromosomal assignment of hepatitis B virus integration sites. (1985) (32)
Study of an additional 58 DNA markers in five human populations from four continents. (1991) (31)
A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5.1 centimorgans. (1991) (31)
Management of resectable colorectal lung metastases (2016) (30)
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites. (1994) (30)
SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis. (2004) (29)
The Tetratricopeptide Repeat Domain 7 Gene is Mutated in Flaky Skin Mice: A Model for Psoriasis, Autoimmunity, and Anemia (2005) (29)
Human gastric cathepsin E gene. Multiple transcripts result from alternative polyadenylation of the primary transcripts of a single gene locus at 1q31-q32. (1992) (29)
Inhibitory KIR3DL1 alleles are associated with psoriasis (2016) (27)
Meta-Analysis of the TNFAIP3 Region in Psoriasis Reveals a Risk Haplotype that is Distinct from Other Autoimmune Diseases (2014) (27)
Deletion of the activating NKG2C receptor and a functional polymorphism in its ligand HLA‐E in psoriasis susceptibility (2013) (26)
A 12 megabase restriction map at the cystic fibrosis locus. (1989) (25)
Psoriasis genetics: the way forward. (2004) (25)
Understanding the pathogenesis of psoriasis, psoriatic arthritis, and autoimmunity via a fusion of molecular genetics and immunology (2005) (25)
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities. (2013) (23)
Mutations in the Novel Protein PRRT2 Cause Infantile Convulsions with Paroxysmal Kinesigenic Dyskinesia (2012) (23)
A FINE-STRUCTURE LINKAGE MAP FOR CHROMOSOME-13 (1989) (22)
High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q. (1988) (21)
Protective Effect of Human Endogenous Retrovirus K dUTPase Variants on Psoriasis Susceptibility (2012) (21)
Abstracts for the committee on the genetic constitution of chromosome 1 (1991) (21)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. (1990) (21)
Familial and Somatic BAP1 Mutations Inactivate ASXL1/2-Mediated Allosteric Regulation of BAP1 Deubiquitinase by Targeting Multiple Independent Domains. (2018) (20)
Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11–q22.3 (2006) (20)
Direct selection of expressed sequences within a 1-Mb region flanking BRCA1 on human chromosome 17q21. (1995) (19)
Contribution of genetic factors for melanoma susceptibility in sporadic US melanoma patients (2009) (19)
Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitis. (2005) (19)
Infrequency of BRCA2 alterations in head and neck squamous cell carcinoma (1997) (19)
Absence of HOXD10 Mutations in Idiopathic Clubfoot and Sporadic Vertical Talus (2007) (19)
In vitro transformation of cell lines from human salivary gland tumors (1999) (18)
Amplification and characterization of the retinoblastoma gene VNTR by PCR. (1992) (18)
Pleomorphic adenoma gene 1 is expressed in cultured benign and malignant salivary gland tumor cells. (1999) (18)
Influence of Crohn's Disease Risk Alleles and Smoking on Disease Location (2011) (18)
DNA copy number changes as diagnostic tools for lung cancer (2013) (17)
The growth hormone receptor gene in the African pygmy. (1989) (16)
Primary ciliary dyskinesia in Amish communities. (2010) (16)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 (1989) (16)
Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families. (1986) (15)
An alpha satellite DNA polymorphism specific for the centromeric region of chromosome 13. (1990) (14)
Loss of heterozygosity for chromosome 22 DNA sequences in human meningioma. (1991) (14)
A high-resolution annotated physical map of the human chromosome 13q12-13 region containing the breast cancer susceptibility locus BRCA2. (1996) (14)
Molecular cloning of BRCA1: a gene for early onset familial breast and ovarian cancer (1993) (14)
JAK3 maps to human chromosome 19p12 within a cluster of proto-oncogenes and transcription factors. (1997) (14)
Integrative Copy Number Analysis of Uveal Melanoma Reveals Novel Candidate Genes Involved in Tumorigenesis Including a Tumor Suppressor Role for PHF10/BAF45a (2019) (13)
Genetic locus for psoriasis identified. (1995) (13)
The NGF and kallikrein genes of mouse, the African rat Mastomys natalensis and man: their distribution and mode of expression in the salivary gland. (1988) (13)
A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus. (1993) (13)
The Molecular Revolution in Cutaneous Biology: The Era of Genome-Wide Association Studies and Statistical, Big Data, and Computational Topics. (2017) (12)
A PstI polymorphism for the human erythrocyte surface protein band 3 (EPB3) demonstrates close linkage of EPB3 to the nerve growth factor receptor. (1989) (12)
Km typing with PCR: application to population screening. (1991) (12)
The tumor genetics of acral melanoma: What should a dermatologist know? (2020) (12)
Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer. (1990) (11)
Polymorphism and mapping of the IGF1 gene, and absence of association with stature among African Pygmies (1990) (11)
CARD14E138A signalling in keratinocytes induces TNF-dependent skin and systemic inflammation (2020) (11)
Runx Transcription Factors Repress Human and Murine c-Myc Expression in a DNA-Binding and C-Terminally Dependent Manner (2013) (11)
Genome-wide association studies and infectious disease. (2010) (10)
Targeting skin: vitiligo and autoimmunity. (2012) (10)
Report of the committee on the genetic constitution of chromosome 13. (1990) (10)
An RFLP associated with pcDLeu2-14, a human T-cell differentiation antigen CD8 (Leu2) cDNA mapped to 2p12. (1986) (9)
Localization of the human c-mos gene by in situ hybridization in two cases of acute nonlymphocytic leukemia type M2. (1987) (9)
Abstracts for the committee on comparative gene mapping (1991) (9)
A somatic cell hybrid map of human chromosome 13. (1993) (9)
Gain of function p.E138A alteration in Card14 leads to psoriasiform skin inflammation and implicates genetic modifiers in disease severity. (2019) (9)
Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes (1999) (9)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 27 of 27) (1991) (9)
Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs (2020) (9)
Zeroing in on tolerance (2001) (9)
Molecular profiling of colorectal pulmonary metastases and primary tumours: implications for targeted treatment (2017) (8)
Markers and methods for reconstructing modern human history. (1998) (8)
Molecular profiling of colorectal pulmonary metastases and primary tumours: implications for targeted treatment. (2017) (8)
Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation. (2005) (8)
CARD14‐associated papulosquamous eruption (CAPE) in pediatric patients: Three additional cases and review of the literature (2021) (8)
RFLPs associated with MDR2, a member of the human multidrug resistance gene family mapped to chromosome 7. (1987) (8)
Genome-wide scan and schizophrenia in African Americans (1998) (8)
Additional evidence of a locus for complex febrile and afebrile seizures on chromosome 12q22-23.3 (2006) (8)
An SspI RFLP at the D13S25 locus identified by the anonymous single copy probe H2-42. (1990) (7)
Investigation of the Possible Role of WNT Genes in Human Breast Cancer (1995) (7)
Use of pharmacogenomics in psoriasis (2011) (7)
Human carboxypeptidase A identifies a BglII RFLP and maps to 7q31-qter. (1990) (7)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
The pro alpha 1 (IV) collagen gene is linked to the D13S3 locus at the distal end of human chromosome 13q. (1987) (6)
Ovarian tumors display persistent microsatellite instability caused by mutation in the mismatch repair gene hMSH-2. (1994) (6)
Canonical and Interior Circular RNAs Function as Competing Endogenous RNAs in Psoriatic Skin (2021) (6)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 6 of 14) (1990) (6)
A highly informative polymorphism of the pepsinogen C gene detected by polymerase chain reaction. (1991) (6)
HLA genes in familial psoriasis vulgaris (PV): Evidence for genetic heterogeneity (1994) (5)
Integrated genomics point to immune vulnerabilities in pleural mesothelioma (2021) (5)
The Immunogenetics of Inflammatory Skin Disease (2004) (5)
Hereditary Breast Cancer Genes (1999) (5)
Dinucleotide repeat polymorphism at the D1S167 locus. (1992) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3) (1991) (5)
Abstracts for the committee on the genetic constitution of chromosome 17 (1991) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Detection of a polymorphism within the pepsinogen C gene with PCR: construction of a linkage map around PGC from 6p11-6p21.3. (1992) (4)
Further evidence for psoriasis susceptibility loci on chromosomes 6p21 and 17q and evidence for novel candidate regions at 1q21–q23, 4q13–q21 and 14q31 (1998) (4)
The single copy probe pG24E2.4 [D13S21] reveals a Bsp1286 RFLP at 13q14.1-q14.2. (1989) (4)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 14 of 14) (1990) (4)
Abstracts for the committee on the genetic constitution of chromosome 2 (1991) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
A new human RFLP identified by 7D2 places D13S10 proximal to esterase D. (1987) (4)
A high frequency RFLP identified by an anonymous single copy genomic clone at 13q14.1-13q14.2 [HGM8 assignment no. D13S22] (1987) (4)
Polymorphisms revealed by random probe H2-10 [D13S26] which maps to chromosome 13q21-q22. (1988) (4)
Abstracts for the committee on the genetic constitution of chromosome 6 (1991) (4)
Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease (1988) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Report of the First International Workshop on Human Chromosome 13 Mapping 1992 (1993) (4)
Abstracts for the committee on the genetic constitution of chromosome 12 (1991) (3)
W1122 Serology Testing, Genotype, and Other Risk Factors for Repeat Ileocolic Resection in Crohn's Disease: A Time-to-Event Analysis (2008) (3)
Circulating tumor DNA is readily detectable among Ghanaian breast cancer patients supporting non-invasive cancer genomic studies in Africa (2020) (3)
Genome-wide association analysis of psoriatic arthritis (2014) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Dinucleotide repeat polymorphism at the D6S223 locus. (1992) (3)
Reproducible Novel Transcriptional Differences Between Psoriatic Lesional and Non-Lesional Skin Show Increased Inflammation and Metabolism. (2015) (3)
The CEPH consortium linkage map of human chromosome 15q. (1992) (3)
The anonymous probe pR1-4 which identifies the locus D13S59 detects a BanII RFLP. (1989) (3)
The CEPH consortium linkage map of human chromosome 13. (1993) (3)
The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with SspI. (1989) (3)
HLA-DQa allelic frequencies detected with PCR in a variety of human populations. (1992) (3)
Abstracts for the committee on chromosomal changes in neoplasia (1991) (3)
Further data on linkage between cystic fibrosis and 7C22 (D7S16) (1987) (3)
Abstracts for the committee on the genetic constitution of chromosome 15 (1991) (3)
Multiple therapeutic pathways in malignant mesothelioma identified by genomic mapping (2020) (2)
The anonymous probe pF5A identifying the locus D13S61 detects RFLPs with XmnI and BanII. (1989) (2)
Nonrandom distribution of N-myc oncogene genotypes in neuroblastoma. (1991) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 9 of 14) (1990) (2)
MA23.10 Low Number of Mutations and Frequent Co-Deletions of CDKN2A and IFN Type I Characterize Malignant Pleural Mesothelioma (2019) (2)
High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13 q ( DNA polymorphisms / chromosome 13 / linkage / haplotypes / linkage disequilibrium (2)
Abstracts for the committee on the genetic constitution of chromosome 22 (1991) (2)
Erratum: Getting under the skin: the immunogenetics of psoriasis (2005) (2)
Linkage analysis of the monoamine A and B genes using newly-defined polymorphisms. (1993) (2)
Two RFLPs for the human dihydrofolate reductase gene (DHFR). (1987) (2)
Clinicopathological features and associations in a series of South African acral melanomas (2021) (2)
Abstracts for the committee on the genetic constitution of chromosome 16 (1991) (2)
The gene for pancreatic polypeptide (PPY) and the anonymous marker D17S78 are within 45 kb of each other on chromosome 17q21. (1994) (2)
Abstracts for the committee on the genetic constitution of chromosome 11 (1991) (2)
Polymerase chain reaction polymorphisms in HLA-DQ alpha and IL6 from Mongoloid and Caucasoid populations. (1991) (2)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27) (1991) (2)
The CA repeat marker D17S791 is located within 40 kb of the WNT3 gene on chromosome 17q. (1993) (2)
Abstracts for the committee on the genetic constitution of chromosome 9 (1991) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 23 of 27) (1991) (1)
The molecular genetics of beta-2 interferon/interleukin-6 (IFN beta 2/IL6) alpha. (1989) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 21 of 27) (1991) (1)
Abstracts for the committee on the genetic constitution of chromosome 7 (2004) (1)
Abstracts for the committee on the genetic constitution of the Y chromosome (1991) (1)
The alpha chain of human propionyl CoA carboxylase (PCCA) mapped to chromosome 13) detects an RFLP with XmnI. (1989) (1)
BAP1 deficiency causes loss of melanocytic cell identity in uveal melanoma (2013) (1)
Abstracts for the committee on the genetic constitution of chromosome 13 (1991) (1)
Correction: AKT inhibitors promote cell death in cervical cancer through disruption of mTOR signaling and glucose uptake (PLoS One.(2014)9:4 (e92948)Doi: 10.1371/journal.pone.0092948) (2016) (1)
Chromosome 8p Status Predicts Disease-Free Survival in Aggressive Class 2 Uveal Melanomas (2007) (1)
Breast Cancer Genes (1997) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 22 of 27) (1991) (1)
Abstracts for the committee on the genetic constitution of chromosome 4 (1991) (1)
Montagna symposium 2008: the biologic basis of psoriasis. (2009) (1)
Loss of Heterozygosity of Chromosome 3 Detected with Single Nucleotide Polymorphisms Is Superior to Monosomy 3 for PredictingMetastasis in Uveal Melanoma (2007) (1)
Faculty Opinions recommendation of Gene expression differences in quiescent versus regenerating hair cells of avian sensory epithelia: implications for human hearing and balance disorders. (2003) (1)
Cystic fibrosis: diagnostic testing and the search for the gene. (1989) (1)
Report of the First International Workshop on Human Chromosome 13 Mapping. Dallas, Texas, September 21-22, 1992. (1993) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27) (1991) (1)
Contents Vol. 55, 1990 (1990) (1)
Investigation of KIR gene associations within two disease groups—Type I diabetes and psoriasis (2004) (1)
Contents Vol. 55, 1990 (1990) (1)
Abstracts for the committee on the genetic constitution of chromosome 10 (1991) (1)
OA 03.02 Comprehensive Characterization of Thymic Epithelial Tumor Subtypes Through an Analysis of Somatic Mutations and Copy Number Alterations (2017) (0)
Referee Acknowledgement for 2016 (2017) (0)
Phosphorylated NF-κB (pNF-κB) was upregulated in psoriatic skin and dermal pNF-κB co-localized with CARD14 + ECs. (2014) (0)
Assignment of eight human genomic DNA sequences detecting high frequency restriction fragment length polymorphisms (1991) (0)
Faculty Opinions recommendation of Intense and highly localized gene conversion activity in human meiotic crossover hot spots. (2004) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
ZNF750 is a nuclear protein whose promoter sequence variants are found in psoriasis patients (2010) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 17 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 8 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 5 of 14) (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 19 of 27) (1991) (0)
Abstracts for the comparative subcommittee on human and mouse homologies (1991) (0)
Index by Abstract Number (1989) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 7 of 14) (1990) (0)
Review of a Unique Cooperative Undertaking by the Baylor Psoriasis Center, the University of Texas Southwestern Medical Center at Dallas, and the National Psoriasis Tissue Bank (1994) (0)
Exclusion oftheRetinoblastoma GeneandChromosome13q astheSiteofa Primary Lesion forHumanBreast Cancer (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 2 of 14) (1990) (0)
Abstracts for the committee on the genetic constitution of chromosome 5 (1991) (0)
Transfection of psoriasis-associated CARD14 mutations into dermal endothelial cells resulted in increased expression and of several chemokines. (2014) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 3 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 3 of 14) (1990) (0)
MA23.11 Analysis of Immune Phenotype Composition in Malignant Pleural Mesothelioma (MPM) Using Bulk RNA Sequencing (2019) (0)
Subject Index Vol. 44, 1987 (1987) (0)
Genetic Analysis ofCystic Fibrosis: Linkage ofDNA andClassical MarkersinMultiplex Families (1986) (0)
The Genetic Basis of Primary Ciliary Dyskinesia in Amish Communities. (2009) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 7 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 13 of 27) (1991) (0)
BAP1 DE‐UBIQUITINASE IS ALLOSTERICALLY REGULATED BY ASXL1/2: SOMATIC BAP1 MUTATION IN RCC AND OTHER TUMORS INACTIVE THIS REGULATION BY TARGETING MULTIPLE INDEPENDENT DOMAINS: PD46‐01 (2018) (0)
Punctuated evolution of canonical genomic aberrations in uveal melanoma (2018) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 6 of 27) (1991) (0)
Kinetic Characterization of ASXL1/2-Mediated Allosteric Regulation of the BAP1 Deubiquitinase (2021) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 4 of 14) (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 25 of 27) (1991) (0)
Targeted next-generation sequencing of malignant pleural mesothelioma identifies recurrent NRAS oncogene mutations (2018) (0)
Screening for mutations in the BARD1 gene in families with ovarian cancer. (1997) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 4 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 20 of 27) (1991) (0)
P1.04-63 Correlation of Mutations in TP53, CDKN2A and PIK3CA with VISTA Expression in Pleomorphic Lung Carcinoma (2019) (0)
Faculty Opinions recommendation of Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. (2003) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 26 of 27) (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 14 (1991) (0)
Integrated genomics identify novel immunotherapy targets for malignant mesothelioma (2020) (0)
Intratumoral heterogeneity in PD-L1 expression in pleomorphic lung carcinoma: implications for management of stage III disease (2019) (0)
An interaction between NOD2 and smoking revealed in operative recurrence of ileal Crohnʼs disease: O-0022. (2008) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 2 of 27) (1991) (0)
Index by Keyword (1989) (0)
Contents, Vol. 44, 1987 (1987) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 9 of 27) (1991) (0)
National Psoriasis Tissue Bank (1995) (0)
Abstracts for the committee on the genetic constitution of chromosome 19 (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 12 of 27) (1991) (0)
Immune activating effects of stimulation of TLR agonists and cytokines on keratinocytes from a patient with a CARD14 mediated pustular psoriasis (P6283) (2013) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 15 of 27) (1991) (0)
THRAI and DI7S 183 Flank an Interval of <4 cM for the Breast-Ovarian Cancer Gene (BRCA I) on Chromosome 1 7q2 (2006) (0)
Association mapping with a pooled DNA genomic screen of the non-HLA genes in IDDM, RA and MS (1996) (0)
pathogenesispathophysiology: current concepts of (2006) (0)
Dermal CARD14 expression in psoriasis (2013) (0)
Subject Index Vol. 58, 1991 (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 11 of 14) (1990) (0)
Km TypingwithPCR:Application toPopulation Screening (1991) (0)
Abstracts for the committee on the mitochondrial genome (1991) (0)
Copy number variations in malignant pleural mesothelioma reveal novel regions of genomic imbalances (2018) (0)
116: Somatic and germline mutations in thymic epithelial tumours and their correlation with histological and clinical phenotypes (2017) (0)
Abstracts for the committee on the genetic constitution of chromosome 20 (1991) (0)
Abstractsfor the informatics committee (1991) (0)
Abstract 81: Studying Ghanian Cancer Genomes Using Cell-free DNA (2021) (0)
Abstracts for the committee on the genetic constitution of chromosome 18 (1991) (0)
Abstracts for the committee on linkage and gene order (1991) (0)
The anonymous DNA probe p7-26 identifying the locus [D7S17], reveals an XmnI polymorphism. (1989) (0)
PD-L1 expression in pleomorphic lung carcinoma with STK11 mutations (2020) (0)
Kinetics characterization of ASXL1/2-mediated allosteric regulation of BAP1 deubiquitinase (2020) (0)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 2 of 3) (2004) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
394 Card14 knockin mouse model of psoriasis and psoriatic arthritis (2016) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 8 of 14) (1990) (0)
Index of GDB source ID numbers (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 12 of 14) (1990) (0)
EVIDENCE FOR THE 8Q CANDIDATE REGION IN SUSCEPTIBILITY TO ADOLESCENT IDIOPATHIC SCOLIOSIS. (2008) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 11 of 27) (1991) (0)
P1.17-019 B7-H3 Protein Expression in Thymic Epithelial Tumor Subtypes and Its Association with PD-L1 and Clinical Characteristics (2017) (0)
Abstracts dscribing resources, technological and other developments (1991) (0)
Increased expression of CARD14-modulated chemokines in psoriatic skin co-localized with dermal endothelial cells. (2014) (0)
Author response: CARD14E138A signalling in keratinocytes induces TNF-dependent skin and systemic inflammation (2020) (0)
Abstractsfor the DNA committee (1991) (0)
55: Somatic BAP1 and NF2 mutations in pleural malignant mesothelioma and their correlation with clinical phenotype (2017) (0)
Subject Index Vol. 62, 1993 (1993) (0)
Correlation between BAP1 Localization, Driver Mutations, and Patient Survival in Uveal Melanoma (2022) (0)
Abstracts for the committee on clinical disorders and chromosomal deletion syndromes (1991) (0)
Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma (2022) (0)
P-138 A comparison of the transcriptomic profiles of matched tissue from primary colorectal cancer and corresponding secondary lung metastases (2020) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 5 of 27) (1991) (0)
Comparison of the genetic profiles of primary colorectal cancers and their subsequent pulmonary metastases: Implications for targeted treatment. (2016) (0)
A Breath of Fresh Air: Opening up the Lung Cancer Genome. (2019) (0)
CARD14-Mediated Psoriasis and Pityriasis Rubra Piliaris (PRP) (2020) (0)
Abstract 3390: Clonal evolution in uveal melanoma (2017) (0)
Abstracts for the committee on the genetic constitution of chromosome 21 (1991) (0)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 (1989) (0)
Linkage of psoriasis to the MHC and evidence for additional loci in a large cohort (International Psoriasis Genetics Consortium). (2002) (0)
Abstracts for the committee on the genetic constitution of chromosome 8 (1991) (0)
Management of resectable colorectal lung metastases (2015) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 10 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 13 of 14) (1990) (0)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 (1989) (0)
Referee acknowledgement for 2017 (2018) (0)
MA21.03 Heterogeneity in MET Copy Number and Intratumoural Subsets in Pleomorphic Lung Carcinoma: Implications for MET Directed Therapy in NSCLC (2018) (0)
Expression of PD-L1, PD-L2 and PD-1 in thymic epithelial tumours (TETs). (2016) (0)
oligonucleotide array revealed by profiling of psoriasis on the 63,100-element Novel mechanisms of T-cell and dendritic cell activation (2016) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 14 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 18 of 27) (1991) (0)

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