PubRank

S Weremowicz

Author PubWeight™ 58.30‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations. Proc Natl Acad Sci U S A 1999 2.70
2 Disruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains. Cell 1995 2.15
3 Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner. Mol Cell Biol 1993 2.05
4 RSK3 encodes a novel pp90rsk isoform with a unique N-terminal sequence: growth factor-stimulated kinase function and nuclear translocation. Mol Cell Biol 1995 1.86
5 Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex. J Clin Invest 2000 1.72
6 Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9. Genomics 1997 1.46
7 Characterization of human and mouse cartilage oligomeric matrix protein. Genomics 1994 1.38
8 Is HMGIC rearranged due to cryptic paracentric inversion of 12q in karyotypically normal uterine leiomyomas? Genes Chromosomes Cancer 1999 1.38
9 An eukaryotic RuvB-like protein (RUVBL1) essential for growth. J Biol Chem 1998 1.37
10 Functional and molecular characterization of the human neutral solute channel aquaporin-9. Am J Physiol 1999 1.37
11 Human calcium transport protein CaT1. Biochem Biophys Res Commun 2000 1.33
12 Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57KIP2. Am J Surg Pathol 2001 1.26
13 Identification, localization, and expression of two novel human genes similar to deoxyribonuclease I. Genomics 1997 1.24
14 Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects. J Biol Chem 1998 1.22
15 Human vitamin C (L-ascorbic acid) transporter SVCT1. Biochem Biophys Res Commun 2000 1.22
16 A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mapping. Genomics 2000 1.19
17 Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case. Mod Pathol 2002 1.18
18 Ribonucleolytic activity of angiogenin: essential histidine, lysine, and arginine residues. Proc Natl Acad Sci U S A 1987 1.15
19 The human homolog of Saccharomyces cerevisiae CDC45. J Biol Chem 1998 1.14
20 SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseases. Genomics 2000 1.06
21 Cytogenetic abnormalities in uterine myomas are associated with myoma size. Mol Hum Reprod 1998 1.06
22 Chromosomal translocation t(8;12) induces aberrant HMGIC expression in aggressive angiomyxoma of the vulva. Genes Chromosomes Cancer 2001 1.05
23 Isolation and chromosomal localization of the human endothelial nitric oxide synthase (NOS3) gene. Genomics 1994 1.05
24 Novel isoform of lymphoid adaptor FYN-T-binding protein (FYB-130) interacts with SLP-76 and up-regulates interleukin 2 production. J Biol Chem 1999 1.05
25 Structure and chromosomal assignment of the human cathepsin K gene. Genomics 1997 1.02
26 Genomic organization, complete sequence, and chromosomal location of the gene for human eotaxin (SCYA11), an eosinophil-specific CC chemokine. Genomics 1997 0.98
27 Cloning of human RTEF-1, a transcriptional enhancer factor-1-related gene preferentially expressed in skeletal muscle: evidence for an ancient multigene family. Genomics 1996 0.95
28 Somatic mosaicism for deletion of the entire NF1 gene identified by FISH. Hum Genet 1997 0.92
29 The human ortholog of rhesus mannose-binding protein-A gene is an expressed pseudogene that localizes to chromosome 10. Mamm Genome 1998 0.91
30 Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female. Cytogenet Genome Res 2010 0.90
31 Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: sequence, expression, alternative splicing, and chromosomal localization. Genomics 2000 0.90
32 Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas. Genes Chromosomes Cancer 1996 0.89
33 Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomata. Genomics 1995 0.89
34 Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16q. Diabetes 1995 0.89
35 An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1). Genomics 1997 0.88
36 Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease. Genomics 1995 0.88
37 Expression of two human skeletal calcitonin receptor isoforms cloned from a giant cell tumor of bone. The first intracellular domain modulates ligand binding and signal transduction. J Clin Invest 1995 0.87
38 The thrombospondin-4 gene. Mamm Genome 1999 0.84
39 Translocations in 7q22 define a critical region in uterine leiomyomata. Cancer Genet Cytogenet 1994 0.82
40 Localization of serum biotinidase (BTD) to human chromosome 3 in band p25. Genomics 1994 0.81
41 Expression of HMGIY in three uterine leiomyomata with complex rearrangements of chromosome 6. Cancer Genet Cytogenet 1999 0.81
42 Balanced translocation of 10q and13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome. J Clin Endocrinol Metab 1999 0.81
43 Assignment of the gene coding for the human high-affinity glutamate transporter EAAC1 to 9p24: potential role in dicarboxylic aminoaciduria and neurodegenerative disorders. Genomics 1994 0.81
44 Localization and expression of the human estrogen receptor beta gene in uterine leiomyomata. Genes Chromosomes Cancer 1998 0.80
45 Assignment of C1QBP encoding the C1q globular domain binding protein (gC1q-R) to human chromosome 17 band p13.3 by in situ hybridization. Cytogenet Cell Genet 1997 0.79
46 A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis. Genes Chromosomes Cancer 2000 0.79
47 Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14. Genes Chromosomes Cancer 2000 0.79
48 STK25 is a candidate gene for pseudopseudohypoparathyroidism. Genomics 2001 0.79
49 Genomic organization and chromosomal localization of the DUSP2 gene, encoding a MAP kinase phosphatase, to human 2p11.2-q11. Genomics 1995 0.78
50 Cloning and expression of a murine histone deacetylase 3 (mHdac3) cDNA and mapping to a region of conserved synteny between murine chromosome 18 and human chromosome 5. Mol Cell Biol Res Commun 1999 0.77
51 Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to chromosome 16p13.3. Genomics 1998 0.77
52 A gene similar to PKD1 maps to chromosome 4q22: a candidate gene for PKD2. Genomics 1996 0.76
53 The protein tyrosine phosphatase epsilon gene maps to mouse chromosome 7 and human chromosome 10q26. Genomics 1996 0.76
54 Sites of modification of human angiogenin by bromoacetate at pH 5.5. Biochem Biophys Res Commun 1988 0.76
55 Laboratory investigations on equine influenza during the outbreak in Poland in 1980. Zentralbl Veterinarmed B 1983 0.75
56 Polypeptides of equine influenza virus A/Equi-2/Warszawa/9/69. Zentralbl Veterinarmed B 1980 0.75
57 Fluorescence in situ hybridization for the detection of aneuploidy from archived fetal cells. Obstet Gynecol 1996 0.75
58 Primary parauterine leiomyoma with a t(6;14) Genes Chromosomes Cancer 1999 0.75
59 [Purification of equine influenza virus A/Equi-2/W/9/69 by the sucrose step density gradient ultracentrifugation]. Med Dosw Mikrobiol 1978 0.75