PubRank

R Siebert

Author PubWeight™ 112.26‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A physical map of the human genome. Nature 2001 12.39
2 Identification of the familial cylindromatosis tumour-suppressor gene. Nat Genet 2000 3.42
3 The BCL11 gene family: involvement of BCL11A in lymphoid malignancies. Blood 2001 2.77
4 Inactivating mutations and overexpression of BCL10, a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32). Nat Genet 1999 1.96
5 An imprinted locus associated with transient neonatal diabetes mellitus. Hum Mol Genet 2000 1.73
6 Variable frequencies of MALT lymphoma-associated genetic aberrations in MALT lymphomas of different sites. Leukemia 2004 1.59
7 Recurrent finding of the FIP1L1-PDGFRA fusion gene in eosinophilia-associated acute myeloid leukemia and lymphoblastic T-cell lymphoma. Leukemia 2007 1.43
8 Translocations involving 8q24 in Burkitt lymphoma and other malignant lymphomas: a historical review of cytogenetics in the light of todays knowledge. Leukemia 2008 1.43
9 Loss of the tissue-specific proapoptotic BH3-only protein Nbk/Bik is a unifying feature of renal cell carcinoma. Cell Death Differ 2006 1.39
10 Disruption of the BCL11B gene through inv(14)(q11.2q32.31) results in the expression of BCL11B-TRDC fusion transcripts and is associated with the absence of wild-type BCL11B transcripts in T-ALL. Leukemia 2005 1.39
11 Cyclin D3 is a target gene of t(6;14)(p21.1;q32.3) of mature B-cell malignancies. Blood 2001 1.36
12 A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus. Hum Genet 2006 1.35
13 High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome. J Med Genet 2007 1.34
14 Inv(2)(p23q35) in anaplastic large-cell lymphoma induces constitutive anaplastic lymphoma kinase (ALK) tyrosine kinase activation by fusion to ATIC, an enzyme involved in purine nucleotide biosynthesis. Blood 2000 1.24
15 Gene expression profiling suggests primary central nervous system lymphomas to be derived from a late germinal center B cell. Leukemia 2007 1.18
16 Molecular analysis of the CALM/AF10 fusion: identical rearrangements in acute myeloid leukemia, acute lymphoblastic leukemia and malignant lymphoma patients. Leukemia 2000 1.18
17 Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease. Leukemia 2012 1.17
18 The DNA sequence and comparative analysis of human chromosome 10. Nature 2004 1.14
19 Eμ/miR-125b transgenic mice develop lethal B-cell malignancies. Leukemia 2011 1.14
20 Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32). Leukemia 2007 1.10
21 Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. Clin Genet 2010 1.10
22 Mapping of the gene encoding human beta-defensin-2 (DEFB2) to chromosome region 8p22-p23.1. Genomics 1997 1.05
23 Expression profile of human defensins and antimicrobial proteins in oral tissues. J Oral Pathol Med 2001 1.04
24 Gains of the proto-oncogene BCL11A and nuclear accumulation of BCL11A(XL) protein are frequent in primary mediastinal B-cell lymphoma. Leukemia 2006 1.04
25 Chromosomal abnormalities in nodal and extranodal CD30+ anaplastic large cell lymphomas: infrequent detection of the t(2;5) in extranodal lymphomas. Genes Chromosomes Cancer 1998 1.04
26 A 3-cM commonly deleted region in 6q21 in leukemias and lymphomas delineated by fluorescence in situ hybridization. Genes Chromosomes Cancer 2000 1.02
27 High incidence of chromosomal imbalances and gene amplifications in the classical follicular variant of follicle center lymphoma. Blood 1996 1.01
28 A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation. Leukemia 2007 1.00
29 Modern concepts in the biology, diagnosis, differential diagnosis and treatment of primary central nervous system lymphoma. Leukemia 2011 0.99
30 Detection of translocations affecting the BCL6 locus in B cell non-Hodgkin's lymphoma by interphase fluorescence in situ hybridization. Leukemia 2001 0.98
31 Molecular analysis of single B cells from T-cell-rich B-cell lymphoma shows the derivation of the tumor cells from mutating germinal center B cells and exemplifies means by which immunoglobulin genes are modified in germinal center B cells. Blood 1999 0.98
32 High expression of several tyrosine kinases and activation of the PI3K/AKT pathway in mediastinal large B cell lymphoma reveals further similarities to Hodgkin lymphoma. Leukemia 2007 0.97
33 Mutation of an IKK phosphorylation site within the transactivation domain of REL in two patients with B-cell lymphoma enhances REL's in vitro transforming activity. Oncogene 2006 0.97
34 Biallelic inactivation of TRAF3 in a subset of B-cell lymphomas with interstitial del(14)(q24.1q32.33). Leukemia 2009 0.97
35 Partial uniparental disomy: a recurrent genetic mechanism alternative to chromosomal deletion in malignant lymphoma. Leukemia 2006 0.96
36 Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13. Hum Genet 2000 0.95
37 ALK-positive diffuse large B-cell lymphoma with ALK-Clathrin fusion belongs to the spectrum of pediatric lymphomas. Leukemia 2005 0.94
38 Molecular-cytogenetic comparison of mucosa-associated marginal zone B-cell lymphoma and large B-cell lymphoma arising in the gastro-intestinal tract. Genes Chromosomes Cancer 2001 0.94
39 Unfavourable prognosis of patients with trisomy 18q21 detected by fluorescence in situ hybridisation in t(11;18) negative, surgically resected, gastrointestinal B cell lymphomas. J Clin Pathol 2004 0.94
40 Molecular cytogenetic detection of chromosomal breakpoints in T-cell receptor gene loci. Leukemia 2003 0.94
41 High frequency of the N34S mutation in the SPINK1 gene in chronic pancreatitis detected by a new PCR-RFLP assay. Am J Med Genet 2001 0.94
42 Loss of a novel tumor suppressor gene locus at chromosome 8p is associated with leukemic mantle cell lymphoma. Blood 2001 0.93
43 Segmental chromosomal aberrations and centrosome amplifications: pathogenetic mechanisms in Hodgkin and Reed-Sternberg cells of classical Hodgkin's lymphoma? Leukemia 2003 0.93
44 Array-based DNA methylation analysis in classical Hodgkin lymphoma reveals new insights into the mechanisms underlying silencing of B cell-specific genes. Leukemia 2011 0.92
45 Toward humanizing adoption. Child Welfare 1982 0.92
46 Frequent deletions of 6q23-24 in B-cell non-Hodgkin's lymphomas detected by fluorescence in situ hybridization. Genes Chromosomes Cancer 1997 0.91
47 Pathway activation patterns in diffuse large B-cell lymphomas. Leukemia 2008 0.91
48 Clinicopathogenetic significance of chromosomal abnormalities in patients with blastic peripheral B-cell lymphoma. Kiel-Wien-Lymphoma Study Group. Blood 1999 0.91
49 Multipotent cells of monocytic origin improve damaged heart function. Am J Transplant 2006 0.91
50 Lack of somatic hypermutation of IG V(H) genes in lymphoid malignancies with t(2;14)(p13;q32) translocation involving the BCL11A gene. Leukemia 2002 0.90
51 Rapid amplification of immunoglobulin heavy chain switch (IGHS) translocation breakpoints using long-distance inverse PCR. Leukemia 2004 0.90
52 Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma. Leukemia 2009 0.89
53 Deletions in the long arm of chromosome 10 in lymphomas with t(14;18): a pathogenetic role of the tumor supressor genes PTEN/MMAC1 and MXI1? Blood 1998 0.89
54 Familial Williams-Beuren syndrome showing varying clinical expression. Am J Med Genet 2001 0.89
55 Clinical and morphologic features of B-cell small lymphocytic lymphoma with del(6)(q21q23). Blood 1994 0.88
56 Strong BCL10 nuclear expression identifies gastric MALT lymphomas that do not respond to H pylori eradication. Gut 2006 0.88
57 Base-pair resolution DNA methylome of the EBV-positive Endemic Burkitt lymphoma cell line DAUDI determined by SOLiD bisulfite-sequencing. Leukemia 2013 0.88
58 Chromosomal abnormalities clustering in multiple myeloma reveals cytogenetic subgroups with nonrandom acquisition of chromosomal changes. Leukemia 2004 0.87
59 Androgen receptor mutations are associated with altered epigenomic programming as evidenced by HOXA5 methylation. Sex Dev 2011 0.86
60 Homozygous deletion of SOCS1 in primary mediastinal B-cell lymphoma detected by CGH to BAC microarrays. Leukemia 2005 0.85
61 Identification of nucleolar protein No55 as a tumour-associated autoantigen in patients with prostate cancer. Br J Cancer 2000 0.85
62 Cytogenetical assignment and physical mapping of the human R-PTP-kappa gene (PTPRK) to the putative tumor suppressor gene region 6q22.2-q22.3. Genomics 1998 0.85
63 An easy and reliable procedure of microdissection technique for the analysis of chromosomal breakpoints and marker chromosomes. Chromosome Res 1999 0.85
64 Expression pattern of intracellular leukocyte-associated proteins in primary mediastinal B cell lymphoma. Leukemia 2005 0.85
65 Feasibility of simultaneous fluorescence immunophenotyping and fluorescence in situ hybridization study for the detection of estrogen receptor expression and deletions of the estrogen receptor gene in breast carcinoma cell lines. Virchows Arch 2000 0.85
66 Complex variant translocation t(1;2) with TPM3-ALK fusion due to cryptic ALK gene rearrangement in anaplastic large-cell lymphoma. Blood 1999 0.84
67 Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia. Gene 2002 0.83
68 Cytogenetic and molecular characterization of a patient with simultaneous B-cell chronic lymphocytic leukemia and peripheral T-cell lymphoma. Am J Hematol 2001 0.82
69 Development of a positron probe for localization and excision of brain tumours during surgery. Phys Med Biol 2009 0.82
70 Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin. Hum Genet 2003 0.82
71 DiGeorge syndrome with discordant phenotype in monozygotic twins. J Med Genet 2000 0.82
72 Extramedullary manifestation of a donor-derived acute myeloid leukemia in a liver transplant patient. Leukemia 2004 0.82
73 SLP65 deficiency results in perpetual V(D)J recombinase activity in pre-B-lymphoblastic leukemia and B-cell lymphoma cells. Oncogene 2006 0.82
74 Detection of 6q deletions in breast carcinoma cell lines by fluorescence in situ hybridization. Hum Genet 1998 0.82
75 A 439 kb-sized homozygous deletion in 17p13.3 leading to biallelic loss of the ASPA as cause of Canavan disease detected by SNP-array analysis. Mol Genet Metab 2009 0.82
76 Amplification of ERBB2, RARA, and TOP2A genes in a myelodysplastic syndrome transforming to acute myeloid leukemia. Cancer Genet Cytogenet 2001 0.82
77 Inv(11)(q21q23) fuses MLL to the Notch co-activator mastermind-like 2 in secondary T-cell acute lymphoblastic leukemia. Leukemia 2008 0.81
78 The SRC family kinase LYN redirects B cell receptor signaling in human SLP65-deficient B cell lymphoma cells. Oncogene 2006 0.81
79 Diffuse large B-cell lymphoma of Waldeyer's ring has distinct clinicopathologic features: a GELA study. Ann Oncol 2012 0.81
80 Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridization. Cancer Genet Cytogenet 2001 0.80
81 Genetic instability of 3p12-p21-specific microsatellite sequences in renal cell carcinoma. Br J Urol 1996 0.80
82 Sigmoid diverticulitis in patients with Williams-Beuren syndrome: relatively high prevalence and high complication rate in young adults with the syndrome. Am J Med Genet A 2005 0.80
83 Cloning and localization of C2orf2(ropp120), a previously unknown WD repeat protein. Genomics 2000 0.79
84 Molecular cytogenetic analysis of chromosomal breakpoints in the IGH, MYC, BCL6, and MALT1 gene loci in primary cutaneous B-cell lymphomas. J Invest Dermatol 2004 0.79
85 Herniated thoracic disc at T1-T2 with paraparesis. Transthoracic excision and fusion, case report with 4-year follow-up. Spine (Phila Pa 1976) 1993 0.79
86 Integration of amplified BCR/ABL fusion genes into the short arm of chromosome 17 as a novel mechanism of disease progression in chronic myeloid leukemia. Genes Chromosomes Cancer 2001 0.79
87 Cytogenetic and molecular characterization of simultaneous chronic and acute myelocytic leukemia. Cancer Genet Cytogenet 2003 0.79
88 Centrosome abnormalities in ALK-positive anaplastic large-cell lymphoma. Leukemia 2004 0.78
89 Report of a workshop on malignant lymphoma: a review of molecular and clinical risk profiling. Br J Haematol 2008 0.78
90 Peripheral T-cell non-Hodgkin's lymphoma NOS: naming of parts. Leukemia 2006 0.78
91 Towards defining the lymphoma methylome. Leukemia 2006 0.78
92 Bladder exstrophy and extreme genital anomaly in a patient with pure terminal 1q deletion: expansion of phenotypic spectrum. Eur J Med Genet 2011 0.78
93 Detection of secondary genetic aberrations in follicle center cell derived lymphomas: assessment of the reliability of comparative genomic hybridization and standard chromosome analysis. Leukemia 2001 0.78
94 The BCL6 gene in B-cell lymphomas with 3q27 translocations is expressed mainly from the rearranged allele irrespective of the partner gene. Leukemia 2003 0.78
95 Dynamics of single-stranded DNA migration in denaturing polyacrylamide slab-gel electrophoresis. Electrophoresis 2001 0.77
96 Jumping translocation of 1q as the sole aberration in a case of follicular lymphoma. Cancer Genet Cytogenet 1999 0.77
97 Evidence for gene recombination in FCGR3 gene variants. Vox Sang 2009 0.77
98 Treatment of aggressive, or progressing indolent peripheral T- and NK-cell neoplasias by combination of fludarabine, cyclophosphamide and doxorubicine. Onkologie 2001 0.76
99 Maternal uniparental disomy 15 in a fetus resulting from a balanced familial translocation t(2;15)(p11;q11.2). Prenat Diagn 2010 0.76
100 No evidence for deletions of the NBS1 gene in lymphomas. Cancer Genet Cytogenet 2001 0.75
101 Short telomeres and high telomerase activity in T-cell prolymphocytic leukemia. Leukemia 2007 0.75
102 Re: B-cell non-Hodgkin's lymphoma: evidence for the t(14;18) translocation in all hematopoietic cell lineages. J Natl Cancer Inst 1997 0.75
103 Lack of deletions of the PTEN/MMAC1 and MXI1 loci in renal cell carcinoma by interphase cytogenetics. Cancer Genet Cytogenet 2000 0.75
104 Frequent allelic loss of the BCL10 gene in lymphomas with the t(11;14)(q13;q32). Leukemia 2001 0.75
105 [1st results of a secretin-pancreozymin short test with endoscopic extraction of pancreatic juice for testing of the exocrine pancreas function]. Z Med Lab Diagn 1983 0.75
106 [Electroencephalographic examinations in emotionally disturbed children and adolescents (author's transl)]. Fortschr Neurol Psychiatr Grenzgeb 1977 0.75
107 Malignant melanoma and Wiedemann-Beckwith syndrome in childhood. Klin Padiatr 2010 0.75
108 Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. Epilepsy Res 2006 0.75
109 [Australia-(SH-) antigen screening test in hospitals]. Z Arztl Fortbild (Jena) 1971 0.75
110 [German woman physician supports medical continued education in East Indonesia; Vera Kaas en the dream of Sumba]. Dtsch Krankenpflegez 1976 0.75
111 [Experiences with a new microliter system (KAPA) in the determination of threshold values for transaminase activity in the clinical laboratory]. Dtsch Gesundheitsw 1972 0.75
112 [Between fetishism and aspirin. Medicine men of the 3d world as important assistants in public health]. Dtsch Krankenpflegez 1975 0.75
113 BCR rearrangement without juxtaposition of ABL in pre-T acute lymphoblastic leukaemia. Br J Haematol 1996 0.75
114 [Model of the interpretation process in the visual analysis of orienting tests]. Z Med Lab Diagn 1986 0.75
115 Autosomal dominant Parkinson's disease in a large German pedigree. Acta Neurol Scand 2011 0.75
116 Lymphoma 'type K.'-in memory of Karl Lennert (1921-2012). Leukemia 2013 0.75
117 Characterization and chromosomal assignment of yeast artificial chromosomes containing human 3p13-p21-specific sequence tagged sites. Cancer Genet Cytogenet 1995 0.75
118 [Indicators of changes in the pancreatic ducts and parenchyma]. Z Med Lab Diagn 1984 0.75
119 [Diagnosis of pancreas function by electrolyte and trace element determination in endoscopically obtained pancreatic juice following secretin/pancreozymin stimulation]. Z Med Lab Diagn 1983 0.75
120 [Insulin determination in pure pancreatic juice following secretin-pancreozymin stimulation]. Z Med Lab Diagn 1984 0.75
121 Construction of a consistent YAC contig for human chromosome region 3p14.1. Genome Res 1996 0.75
122 Radioactive iodine uptake test. Southwest Med 1971 0.75
123 [A simple method of osmotic concentration]. Dtsch Gesundheitsw 1972 0.75
124 Eosinophilic cellulitis as a presenting feature of chronic eosinophilic leukaemia, secondary to a deletion on chromosome 4q12 creating the FIP1L1-PDGFRA fusion gene. Br J Dermatol 2006 0.75
125 [FICTION as a new tool to early lung cancer diagnosis]. An Sist Sanit Navar 2003 0.75
126 [Endoscopy supported biochemical pancreatic differential diagnosis within the scope of a diagnosis strategy]. Z Med Lab Diagn 1985 0.75
127 [Conventional and multicolor FICTION as tools for the interdisciplinar study of hematological neoplasms]. An Sist Sanit Navar 2003 0.75
128 Assignment of the human FAN protein gene (NSMAF) to human chromosome region 8q12-->q13 by in situ hybridization. Cytogenet Cell Genet 1999 0.75
129 Mobility and activation energy of single-stranded DNA in denaturing cross-linked polyacrylamide slab gels. J Chromatogr A 2000 0.75
130 A numerical study of persistence length effects on DNA conformation in sequencing electrophoresis. Electrophoresis 1996 0.75
131 [Identification of the steroids described as "6-beta, 15-alpha-dihydroxyprogesterone", "11-alpha, 15-beta-dihydroxyprogesterone" and "12-beta, 15-beta-dihydroxyprogesterone" with 12-beta, 15-alpha-dihydroxyprogesterone]. Helv Chim Acta 1965 0.75
132 Chromosome aberrations are restricted to the CD56+, CD3- tumour cell population in natural killer cell lymphomas: a combined immunophenotyping and FISH study. Br J Haematol 1999 0.75
133 Williams-Beuren syndrome 35 years after the diagnosis in one of the first Beuren patients. Am J Med Genet 2000 0.75