Anne-marie Poustka

Anne-marie Poustka's AcademicInfluence.com Rankings

Anne-marie Poustka

Biology

#11343

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#14731

Historical Rank

Genetics

#1222

World Rank

#1323

Historical Rank

Molecular Biology

#1738

World Rank

#1767

Historical Rank

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Biology

Anne-marie Poustka's Degrees

PhD Genetics Stanford University

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Anne-marie Poustka's Published Works

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

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

Published Works

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes (1993) (7826)
Variance stabilization applied to microarray data calibration and to the quantification of differential expression (2002) (2276)
Functional impact of global rare copy number variation in autism spectrum disorders (2010) (1891)
Lambda replacement vectors carrying polylinker sequences. (1983) (1447)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007) (1382)
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping (1990) (1288)
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters (1993) (1129)
The DNA sequence of the human X chromosome (2005) (1072)
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets (1995) (1005)
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions (1998) (913)
Cloning of the T gene required in mesoderm formation in the mouse (1990) (853)
A physical map of the human genome (2001) (753)
A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast (1996) (586)
A genome-wide scan for common alleles affecting risk for autism (2010) (567)
A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium. (1998) (537)
Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti (2000) (531)
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. (2001) (466)
DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3–26.1 is deleted in malignant brain tumours (1997) (452)
Systematic subcellular localization of novel proteins identified by large‐scale cDNA sequencing (2000) (351)
Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (346)
Modeling ERBB receptor-regulated G1/S transition to find novel targets for de novo trastuzumab resistance (2009) (312)
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. (2000) (302)
Serotonin transporter (5-HTT) gene variants associated with autism? (1997) (276)
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene (1996) (249)
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. (1999) (238)
Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal‐Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1 (1999) (220)
Dickkopf genes are co-ordinately expressed in mesodermal lineages (1999) (206)
Cloning of gp-340, a putative opsonin receptor for lung surfactant protein D. (1999) (206)
Parameter estimation for the calibration and variance stabilization of microarray data (2003) (200)
Identification and classification of differentially expressed genes in renal cell carcinoma by expression profiling on a global human 31,500-element cDNA array. (2001) (200)
GOSim – an R-package for computation of information theoretic GO similarities between terms and gene products (2007) (196)
Fragile X syndrome without CCG amplification has an FMR1 deletion (1992) (188)
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder (2011) (186)
Global gene expression analysis reveals specific patterns of cell junctions in non-small cell lung cancer subtypes. (2009) (182)
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. (2001) (181)
A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. (1992) (175)
DMBT1 encodes a protein involved in the immune defense and in epithelial differentiation and is highly unstable in cancer. (2000) (168)
Comprehensive Allelotype and Genetic Analysis of 466 Human Nervous System Tumors (2000) (166)
Regulation of DMBT1 via NOD2 and TLR4 in Intestinal Epithelial Cells Modulates Bacterial Recognition and Invasion1 (2007) (165)
Processing and quality control of DNA array hybridization data (2000) (164)
Identification of a common gene expression signature in dilated cardiomyopathy across independent microarray studies. (2006) (159)
Identification of the Bacteria-binding Peptide Domain on Salivary Agglutinin (gp-340/DMBT1), a Member of the Scavenger Receptor Cysteine-rich Superfamily* (2002) (158)
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM (1994) (153)
A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression. (1999) (153)
Jumping libraries and linking libraries: the next generation of molecular tools in mammalian genetics (1986) (142)
A 15q13.3 microdeletion segregating with autism (2009) (139)
Functional Annotation of Mouse Genome Sequences (2001) (136)
Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. (2001) (126)
A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome. (2002) (125)
The melanoma antigen gene (MAGE) family is clustered in the chromosomal band Xq28. (1995) (124)
Bacteria Binding by DMBT1/SAG/gp-340 Is Confined to the VEVLXXXXW Motif in Its Scavenger Receptor Cysteine-rich Domains* (2004) (123)
Alternative splicing in the fragile X gene FMR1. (1993) (122)
Construction and use of human chromosome jumping libraries from NotI-digested DNA (1987) (120)
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions (2000) (119)
Selective isolation of cosmid clones by homologous recombination in Escherichia coli. (1984) (118)
A strategy for the selection of transcribed sequences in the Xq28 region. (1992) (118)
Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad. (1993) (116)
A microscope‐based screening platform for large‐scale functional protein analysis in intact cells (2003) (114)
Effects of infiltrating lymphocytes and estrogen receptor on gene expression and prognosis in breast cancer (2009) (114)
The (6;9) chromosome translocation, associated with a specific subtype of acute nonlymphocytic leukemia, leads to aberrant transcription of a target gene on 9q34 (1990) (112)
Prognostic impacts of cytogenetic findings in clear cell renal cell carcinoma: gain of 5q31-qter predicts a distinct clinical phenotype with favorable prognosis. (2001) (112)
Combinatorial synthesis of peptide arrays with a laser printer. (2008) (107)
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism (2006) (101)
Mutation analysis of the coding sequence of the MECP2 gene in infantile autism (2002) (101)
A Compendium to Ensure Computational Reproducibility in High-Dimensional Classification Tasks (2004) (101)
The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcripts. (1998) (99)
DMBT1 confers mucosal protection in vivo and a deletion variant is associated with Crohn's disease. (2007) (97)
Molecular cloning of tissue-specific transcripts of a transketolase-related gene: implications for the evolution of new vertebrate genes. (1996) (96)
Gene expression in kidney cancer is associated with cytogenetic abnormalities, metastasis formation, and patient survival. (2005) (95)
Deleted in Malignant Brain Tumors 1 is a versatile mucin-like molecule likely to play a differential role in digestive tract cancer. (2001) (95)
Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue. (2005) (94)
Human histone gene organization: nonregular arrangement within a large cluster. (1997) (91)
Recombination events suggest potential sites for the Huntington's disease gene (1989) (88)
Systematic analysis of T7 RNA polymerase based in vitro linear RNA amplification for use in microarray experiments (2004) (88)
The genomic structure of the DMBT1 gene: evidence for a region with susceptibility to genomic instability (1999) (88)
Analysis of cosmids using linearization by phage lambda terminase. (1985) (88)
SMART amplification combined with cDNA size fractionation in order to obtain large full-length clones (2004) (85)
The Murine GABAA Receptor δ-Subunit Gene: Structure and Assignment to Human Chromosome 1 (1990) (84)
Infrared‐based protein detection arrays for quantitative proteomics (2007) (81)
Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs (2001) (81)
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q (2005) (79)
Genomic organization of the adrenoleukodystrophy gene. (1994) (78)
CRP‐ductin, the mouse homologue of gp‐340/deleted in malignant brain tumors 1 (DMBT1), binds gram‐positive and gram‐negative bacteria and interacts with lung surfactant protein D (2003) (77)
Down‐regulation of HLA Class I and NKG2D ligands through a concerted action of MAPK and DNA methyltransferases in colorectal cancer cells (2009) (76)
Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome. (2000) (74)
Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1. (1995) (73)
Genomic structure of a novel chloride channel gene, CLIC2, in Xq28. (1997) (72)
Transcriptional organization of a 450-kb region of the human X chromosome in Xq28. (1993) (71)
Differential expression of apoptotic genes PDIA3 and MAP3K5 distinguishes between low- and high-risk prostate cancer (2009) (71)
Dyskerin localizes to the nucleolus and its mislocalization is unlikely to play a role in the pathogenesis of dyskeratosis congenita. (1999) (70)
Molecular approaches to mammalian genetics. (1986) (68)
High-content screening microscopy identifies novel proteins with a putative role in secretory membrane traffic. (2004) (68)
Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries. (1995) (67)
Candidate genes for cross-resistance against DNA-damaging drugs. (2002) (66)
Identifying splits with clear separation: a new class discovery method for gene expression data (2001) (66)
A gene in human chromosome band Xq28 (GABRE) defines a putative new subunit class of the GABAA neurotransmitter receptor. (1997) (64)
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region. (1996) (64)
New genes in the class II region of the human major histocompatibility complex. (1991) (63)
Pore membrane and/or filament interacting like protein 1 (POMFIL1) is predominantly expressed in the nervous system and encodes different protein isoforms. (2002) (63)
Sequential changes of the DMBT1 expression and location in normal lung tissue and lung carcinomas (2002) (63)
Large‐scale protein expression for proteome research (2005) (61)
DMBT1 functions as pattern‐recognition molecule for poly‐sulfated and poly‐phosphorylated ligands (2009) (59)
High‐resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith‐Magenis region, an unstable region in chromosome band 17p11.2 (1997) (57)
arrayMagic: two-colour cDNA microarray quality control, preprocessing (2005) (57)
Large scale statistical inference of signaling pathways from RNAi and microarray data (2007) (56)
Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport. (1995) (56)
Combinatorial RNAi for quantitative protein network analysis (2007) (56)
Dyskeratosis congenita caused by a 3' deletion: germline and somatic mosaicism in a female carrier. (1999) (55)
DMBT1 expression is down-regulated in breast cancer (2004) (55)
Subtractive gene expression profiling of articular cartilage and mesenchymal stem cells: serpins as cartilage-relevant differentiation markers. (2008) (54)
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region. (1994) (53)
Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients (1997) (53)
Construction of a transcription map of a 300 kb region around the human G6PD locus by direct cDNA selection. (1993) (53)
A gene for FG syndrome maps in the Xq12-q21.31 region. (1997) (51)
Highly homologous loci on the X and Y chromosomes are hot–spots for ectopic recombinations leading to XX maleness (1994) (51)
Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours. (1998) (51)
Identification of cellular targets for the human papillomavirus E6 and E7 oncogenes by RNA interference and transcriptome analyses (2007) (51)
Reduced expression of vacuole membrane protein 1 affects the invasion capacity of tumor cells (2007) (49)
LIFEdb: a database for functional genomics experiments integrating information from external sources, and serving as a sample tracking system (2004) (49)
Frequent downregulation of DMBT1 and galectin‐3 in epithelial skin cancer (2003) (49)
From ORFeome to biology: a functional genomics pipeline. (2004) (49)
Identification and meta‐analysis of a small gene expression signature for the diagnosis of estrogen receptor status in invasive ductal breast cancer (2006) (49)
Estimating large-scale signaling networks through nested effect models with intervention effects from microarray data (2008) (49)
Genetic mapping in mice identifies DMBT1 as a candidate modifier of mammary tumors and breast cancer risk. (2007) (48)
Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3 (1992) (48)
Differential transcriptional regulation of the monocyte-chemoattractant protein-1 (MCP-1) gene in tumorigenic and non-tumorigenic HPV 18 positive cells: The role of the chromatin structure and AP-1 composition (2000) (48)
Analysis of genetic variations of protein tyrosine kinase fyn and their association with alcohol dependence in two independent cohorts (2003) (48)
The SRCR/SID region of DMBT1 defines a complex multi‐allele system representing the major basis for its variability in cancer (2002) (47)
Functional characterization of DNase X, a novel endonuclease expressed in muscle cells. (2000) (47)
Marked gene transcript level alterations occur early during radical prostatectomy. (2008) (47)
Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q) (1999) (47)
Systematic comparison of surface coatings for protein microarrays (2005) (45)
Extraction and processing of high quality RNA from impalpable and macroscopically invisible prostate cancer for microarray gene expression analysis. (2005) (44)
Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare (1991) (44)
γ‐BAR, a novel AP‐1‐interacting protein involved in post‐Golgi trafficking (2005) (44)
A database of germline p53 mutations in cancer-prone families (1998) (43)
Integration of human papillomavirus type 6a DNA in a tonsillar carcinoma: chromosomal localization and nucleotide sequence of the genomic target region. (1994) (41)
Carcinogen inducibility in vivo and down‐regulation of DMBT1 during breast carcinogenesis (2004) (41)
The LIFEdb database in 2006 (2005) (41)
Analysis of pigmented villonodular synovitis with genome-wide complementary DNA microarray and tissue array technology reveals insight into potential novel therapeutic approaches. (2006) (41)
A family of cosmid vectors with the multi-copy R6K replication origin. (1987) (41)
Molecular characterisation of non-absorptive and absorptive enterocytes in human small intestine (2005) (39)
Enhanced Fmr–1 expression in testis (1993) (39)
Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathy. (1997) (39)
1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis. (1998) (39)
International molecular genetic study of autism consortium (IMGSAC). Towards identification of autism susceptibility variants in the IMGSAC sample (2004) (38)
The full-ORF clone resource of the German cDNA Consortium (2007) (37)
Generation of a vector system facilitating cloning of DMBT1 variants and recombinant expression of functional full-length DMBT1. (2005) (37)
Loss of 9p leads to p16INK4A down‐regulation and enables RB/E2F1‐dependent cell cycle promotion in gastrointestinal stromal tumours (GISTs) (2008) (37)
Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes. (1999) (37)
FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome (2009) (37)
Quantitative protein microarrays for time‐resolved measurements of protein phosphorylation (2008) (36)
Utility of lab‐on‐a‐chip technology for high‐throughput nucleic acid and protein analysis (2005) (35)
Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder (2011) (34)
A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers. (1988) (33)
The genomic organization of a human creatine transporter (CRTR) gene located in Xq28. (1996) (33)
Basal transcription activity of the dyskeratosis congenita gene is mediated by Sp1 and Sp3 and a patient mutation in a Sp1 binding site is associated with decreased promoter activity. (2002) (33)
Identification of novel mutations in three families with Emery-Dreifuss muscular dystrophy. (1995) (30)
Extending pathways based on gene lists using InterPro domain signatures (2008) (30)
Site‐characteristic expression and induction of trefoil factor family 1, 2 and 3 and malignant brain tumor‐1 in normal and diseased intrahepatic bile ducts relates to biliary pathophysiology (2004) (30)
BRAF mutations distinguish anorectal from cutaneous melanoma at the molecular level. (2004) (30)
An anthropoid-specific segmental duplication on human chromosome 1q22. (2006) (30)
Human and mouse XAP-5 and XAP-5-like (X5L) genes: identification of an ancient functional retroposon differentially expressed in testis. (1999) (29)
Molecular cancer phenotype in normal prostate tissue. (2009) (29)
Genomic structure of a novel LIM domain gene (ZNF185) in Xq28 and comparisons with the orthologous murine transcript. (1997) (29)
One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC). (2001) (28)
Identification of aberrant chromosomal regions from gene expression microarray studies applied to human breast cancer (2007) (28)
Haplotype analysis of the COMT‐ARVCF gene region in Israeli anorexia nervosa family trios (2005) (28)
Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs. (1997) (28)
A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1). (1996) (27)
Statistical methods and software for the analysis of highthroughput reverse genetic assays using flow cytometry readouts (2006) (27)
Alternative pre-mRNA processing regulates cell-type specific expression of the IL4l1 and NUP62 genes (2005) (27)
Distribution and early development of microarray technology in Europe (1999) (27)
Alternative splicing in the fragile X gene FMR1. (1993) (26)
Transcription mapping in a 700-kb region around the DXS52 locus in Xq28: isolation of six novel transcripts and a novel ATPase isoform (hPMCA5). (1996) (26)
Genomic analysis reveals poor separation of human cardiomyopathies of ischemic and nonischemic etiologies. (2008) (26)
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers (1996) (26)
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]? (2000) (26)
The systematic functional characterisation of Xq28 genes prioritises candidate disease genes (2006) (25)
CDNAs for functional genomics and proteomics: the German Consortium. (2003) (25)
Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1). (1998) (25)
Respiratory Deleted in Malignant Brain Tumours 1 (DMBT1) levels increase during lung maturation and infection (2007) (24)
Point mutation analysis of the FMR-1 gene in autism. (1996) (24)
Automated production of recombinant human proteins as resource for proteome research (2008) (24)
Expression of acyl‐CoA synthetase 5 reflects the state of villus architecture in human small intestine (2004) (23)
High-throughput protein analysis integrating bioinformatics and experimental assays. (2004) (23)
The 5-HT transporter genel inked polymorphic region ( 5H T T L P R ) in evolut ionary perspective : alternative biallelic variation in rhesus m o n k e y s Rapid Communication (23)
Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28. (2002) (23)
An integrative model on the role of DMBT1 in epithelial cancer. (2002) (23)
Predicting pathway membership via domain signatures (2008) (23)
Rare mutations of the DMBT1 gene in human astrocytic gliomas (2002) (23)
Transcriptional analysis of the candidate region for incontinentia pigmenti (IP2) in Xq28. (1996) (22)
Chromosome Jumping: A Long Range Cloning Technique (1988) (22)
Isolation, differential splicing and protein expression of a DNase on the human X chromosome. (1996) (22)
The murine genes Hox-5.1 and Hox-4.1 belong to the same HOX complex on chromosome 2. (1990) (21)
Physical and transcriptional mapping of the 17p13.3 region that is frequently deleted in human cancer. (2000) (21)
X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684). (1994) (21)
Direct visual resolution of gene copy number in the human photopigment gene array. (1999) (21)
In vitro–targeted gene identification in patients with hepatitis C using a genome‐wide microarray technology (2009) (21)
The human glycine receptor beta subunit gene (GLRB): structure, refined chromosomal localization, and population polymorphism. (1998) (20)
Mutation analysis of the coding sequence of the MECP2 gene in infantile autism (2002) (20)
Decrease of Deleted in Malignant Brain Tumour‐1 (DMBT‐1) expression is a crucial late event in intrahepatic cholangiocarcinoma (2003) (20)
Functional profiling: from microarrays via cell-based assays to novel tumor relevant modulators of the cell cycle. (2005) (20)
Association studies of the HOPA dodecamer duplication variant in different subtypes of autism. (2002) (20)
Gene structure and expression of the mouse dyskeratosis congenita gene, dkc1. (2000) (20)
DMBT1 is frequently downregulated in well-differentiated gastric carcinoma but more frequently upregulated across various gastric cancer types. (2007) (19)
Increased KIT signalling with up‐regulation of cyclin D correlates to accelerated proliferation and shorter disease‐free survival in gastrointestinal stromal tumours (GISTs) with KIT exon 11 deletions (2008) (19)
The German cDNA Network: cDNAs, functional genomics and proteomics (2003) (18)
The 3of5 web application for complex and comprehensive pattern matching in protein sequences (2006) (18)
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosome. (1992) (18)
Assignment of CASP81 to human chromosome band 2q33→q34 and Casp82 to the murine syntenic region on chromosome 1B-proximal C by in situ hybridization (1998) (17)
Thioredoxin, a regulator of gene expression (2004) (17)
Discrimination of Direct and Indirect Interactions in a Network of Regulatory Effects (2007) (17)
Allelic variants of CAMTA1 and FLJ10737 within a commonly deleted region at 1p36 in neuroblastoma. (2007) (16)
Identification and characterization of a new gene in the human Xq28 region. (1992) (16)
Direct selection of DNA sequences conserved between species. (1993) (16)
Allelic imbalance and fine mapping of the 17p13.3 subregion in sporadic breast carcinomas. (2001) (16)
Dyskeratosis Congenita Caused by a 3′ Deletion: Germline and Somatic Mosaicism in a Female Carrier (1999) (16)
Physical mapping by PFGE (1990) (15)
Analysis of Losses of Heterozygosity of the Candidate Tumour Suppressor Gene DMBT1 in Melanoma Resection Specimens (2002) (15)
Salivary Agglutinin/DMBT1SAG Expression is Up-regulated in the Presence of Salivary Gland Tumors (2004) (14)
Deleted in Malignant Brain Tumors 1 (DMBT1) is present in hyaline membranes and modulates surface tension of surfactant (2007) (14)
Contact spotting of protein microarrays coupled with spike‐in of normalizer protein permits time‐resolved analysis of ERBB receptor signaling (2008) (14)
IRS-long range (LR) PCR: A simple method for efficient amplification of human genomic DNA from complex sources (1994) (14)
Antibody microarrays as an experimental platform for the analysis of signal transduction networks. (2008) (13)
DMBT1 expression distinguishes anorectal from cutaneous melanoma (2009) (13)
The amphioxus rab GDP-dissociation inhibitor (GDI) gene is neural-specific: implications for the evolution of chordate rab GDI genes. (1999) (13)
Gene expression analysis of endobronchial epithelial lining fluid in the evaluation of indeterminate pulmonary nodules. (2009) (13)
Isolation of human and mouse HMG2a cDNAs: evidence for an HMG2a-specific 3' untranslated region. (1997) (13)
The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3. (1995) (13)
DMBT1 as an archetypal link between infection, inflammation, and cancer (2007) (13)
A 2.3-Mb yeast artificial chromosome contig spanning from Gabra3 to G6pd on the mouse X chromosome. (1994) (13)
Construction of a physical map of an autism susceptibility region in 7q32.3-q33. (2001) (12)
The murine GABAA receptor delta-subunit gene: structure and assignment to human chromosome 1. (1990) (12)
Genetic variation of Aflatoxin B1 aldehyde reductase genes (AFAR) in human tumour cells. (2008) (11)
The scavenging capacity of DMBT1 is impaired by germline deletions (2017) (11)
Expression of Deleted in Malignant Brain Tumor-1 (DMBT1) Molecule in Biliary Epithelium Is Augmented in Hepatolithiasis: Possible Participation in Lithogenesis (2003) (11)
Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI) (1994) (11)
Transcription profiling of renal cell carcinoma. (2002) (10)
Erratum: Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing (EMBO reports (2000) 1 (287-292) DOI: 10.1093/embo-reports/kvd058) (2009) (10)
Isolation of NotI sites from chromosome 22q11. (1993) (10)
High expression level of bone degrading proteins as a possible inducer of osteolytic features in pigmented villonodular synovitis. (2007) (10)
Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1. (1996) (10)
Exclusion of mutations in the MTMR1 gene as a frequent cause of X-linked myotubular myopathy. (2002) (9)
Large-scale mapping and chromosome jumping in the q27 region of the human X chromosome. (1989) (9)
DMBT 1 Encodes a Protein Involved in the Immune Defense and in Epithelial Differentiation and Is Highly Unstable in Cancer 1 (2000) (8)
Estimating Large Scale Scale Signaling Networks through Nested Effects Models from Intervention Effects in Microarray Data (2007) (8)
Reverse‐phase protein arrays for application‐orientated cancer research (2009) (8)
Rapid identification of gene sequences for transcriptional map assembly by direct cDNA screening of genomic reference libraries. (1994) (8)
Construction and use of chromosome jumping libraries. (1993) (7)
The human renin-binding protein gene (RENBP) maps in Xq28. (1994) (7)
Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X Chromosome (2004) (7)
Animal models of autism (2006) (7)
Novel mutations of the DKC1 gene in individuals affected with dyskeratosis congenita. (2010) (6)
Human homologue of the murine bare patches/striated gene is not mutated in incontinentia pigmenti type 2. (2000) (6)
High-Throughput Flow Cytometry–Based Assay to Identify Apoptosis-Inducing Proteins (2007) (6)
Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2. (2000) (6)
Variance Stabilization and Robust Normalization for Microarray Gene Expression Data (2002) (6)
The Human Glycine Receptor Subunit α3 (1998) (6)
Identification of tissue-specific expressed sequences in human band Xq28 with complex pig cDNA probes (1994) (5)
Multiplex reverse transcription‐polymerase chain reaction combined with on‐chip electrophoresis as a rapid screening tool for candidate gene sets (2005) (4)
MIACA – Minimum Information About a Cellular Assay: Standardized description of cell-based functional assay projects (2013) (4)
Molecular characterization of the porcine deleted in malignant brain tumors 1 gene (DMBT1). (2006) (4)
Recent advances in transcription profiling of human cancer. (2004) (3)
Approaching the mouse Steel locus from closely linked molecular markers. (1988) (3)
Systematic subcellular localization of novel proteins identified by large‐scale cDNA sequencing (2009) (2)
Mutation analysis of the DKC1 gene in incontinentia pigmenti (1999) (2)
Correction: Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (2)
Molecular Techniques in Mammalian Genetics: A New Era in Genetic Analysis (1987) (2)
The human rab GDI β gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13 (2009) (2)
DMBT1 (deleted in malignant brain tumors 1) (2011) (2)
CAFTAN: a tool for fast mapping, and quality assessment of cDNAs (2006) (2)
[27] Construction and use of chromosome jumping libraries jumping libraries (1993) (2)
Identification of region-specific cosmid clones by hybridization with pooled Alu-LINE Polymerase Chain Reaction products of Yeast Artificial Chromosome clones (1993) (1)
Large insert linking-clone libraries: construction and use. (1993) (1)
[Microarrays for the identification of molecular markers in the diagnosis and therapy of renal cell carcinomas]. (2006) (1)
Phenotype with Favorable Prognosis qter Predicts a Distinct Clinical − Cell Carcinoma : Gain of 5 q 31 Prognostic Impacts of Cytogenetic Findings in Clear Cell Renal Updated (2001) (1)
Genetic analysis of placental dysplasia in mouse interspecific hybrids (1998) (1)
Modeling breast cell cycle regulation - overcoming drug resistance (2006) (1)
Deleted in Malignant Brain Tumors 1 (2015) (1)
[Molecular high throughput research in prostate carcinoma]. (2007) (1)
Statistical Applications in Genetics and Molecular Biology (2003) (0)
6515 ORAL Transcriptional changes in non-small cell lung cancer are associated with cell adhesion and cell migration processes (2007) (0)
Protein analogous to transketolase. (1996) (0)
Molecular Characterization of the Chromosome 9q34 Breakpoint in Patients with t(6;9) Acute Non-Lymphocytic Leukemia (ANLL) (1990) (0)
Molecular strategies in analysing human mutations (1987) (0)
[454] TARGETED IDENTIFICATION OF IRON REGULATED GENES IN PATIENTS WITH HEMOCHROMATOSIS AND HEPATITIS C USING A CUSTOM-MADE WHOLE GENOME cDNA MICROARRAY (2007) (0)
Bacterial Recognition and Invasion Intestinal Epithelial Cells Modulates via NOD2 and TLR4 in DMBT1 Regulation of (2007) (0)
Development of a rapid screening approach for candidate gene sets in cancer (2005) (0)
Engagement of pro- and antiapoptotic mechanisms in liver cells following administration of chemotherapeutic drugs revealed by microarray analysis (2000) (0)
Custom Megabase Sequencing of a Small Eucaryotic Genome in Germany (1997) (0)
Molecular Genetics of Breast Cancer (2001) (0)
[27] – Large Insert Linking-Clone Libraries: Construction and Use (1995) (0)
Regulated expression of Deleted in malignant brain tumours 1 (DMBT1) in intestinal epithelial cells: a protective mucosal defense mechanism (2005) (0)
Methods and apparatus for applying substances on a carrier, in particular of monomers for combinatorial synthesis of molecular libraries (1999) (0)
Molecular cloning and expression of the mouse Brachyury (T) gene (1989) (0)
GENETIC ANALYSIS OF CIRCADIAN RHYTHM GENES PER1 AND PER2 IN PATIENTS WITH ALCOHOL DEPENDENCE. (2004) (0)
A process for the preparation of protein libraries and selection of proteins from (2001) (0)
Integrated Transcriptional Maps of Large DNA Regions: Towards a Transcriptional Map of Human Chromosome 21 (1994) (0)
YAC CLONING IN GENOME ANALYSIS OF THE HUMAN X-CHROMOSOME (1991) (0)
The use of the microarray-technology in schizophrenia (2002) (0)
Genetic mapping in mice identifies DMBT1 as a candidate modifier of breast cancer risk (2007) (0)
4007 POSTER Molecular and functional profiling for an improved clinical management of prostate cancer (2007) (0)
Human papillomavirus (HPV)-associated carcinogenesis: Identification of putative cellular target genes by RNA interference affecting viral oncogene expression and subsequent transcriptome analysis. (2006) (0)
Multiple Serous Retinal Detachments Seen on Wide-Field Imaging in a Patient With Sympathetic Ophthalmia (2017) (0)
Familial Breast/ovarian Cancer - Progress Towards Isolation of a Predisposing Gene (1994) (0)
Transcriptional mapping by direct cDNA selection: From Xq28 to the entire X chromosome (1994) (0)
Targeted identification of iron regulated genes in patients with hemochromatosis and hepatitis C using a whole genome cDNA microarray (2008) (0)
A gene expression signature suggests molecular alterations preceding prostate tumor manifestation (2008) (0)
The scavenging capacity of DMBT1 is impaired by germline deletions (2017) (0)
DMBT 1 as an archetypal link between infection , inflammation , and cancer (2008) (0)
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder (2011) (0)
Infrared-based protein detection arrays for quantitative proteomics (2008) (0)
Procedure for the production of protein libraries and the selection of proteins from the same. (2001) (0)
Use of Nucleofector ® Technology to Establish Stably Expressing Cell Lines (2004) (0)
From ORFeome to Biology: Identification of Cancer Relevant Modulators of the Cell Cycle (2005) (0)
In the development of the CNS involved protein (TP) (1999) (0)

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