PubRank

D Schindler

Author PubWeight™ 92.35‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Forecasting agriculturally driven global environmental change. Science 2001 16.70
2 Measuring and modelling plant area index in beech stands. Int J Biometeorol 2004 2.23
3 Studies on the mode of action of hygromycin B, an inhibitor of translocation in eukaryotes. Biochim Biophys Acta 1978 2.12
4 The Fanconi anaemia group G gene FANCG is identical with XRCC9. Nat Genet 1998 1.99
5 Brain functional magnetic resonance imaging of rectal pain and activation of endogenous inhibitory mechanisms in irritable bowel syndrome patient subgroups and healthy controls. Gut 2004 1.90
6 Trichodermin resistance--mutation affecting eukaryotic ribosomes. Nature 1974 1.90
7 Mapping of trichodermin resistance in Saccharomyces cerevisiae: a genetic locus for a component of the 60S ribsomal subunit. Genetics 1976 1.75
8 Generation of a mutant form of protein synthesis initiation factor eIF-2 lacking the site of phosphorylation by eIF-2 kinases. Mol Cell Biol 1988 1.69
9 Characterization of ATM gene mutations in 66 ataxia telangiectasia families. Hum Mol Genet 1999 1.66
10 Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction. Cytogenet Genome Res 2002 1.49
11 Overexpression of LASP-1 mediates migration and proliferation of human ovarian cancer cells and influences zyxin localisation. Br J Cancer 2007 1.41
12 Two classes of inhibitors of peptidyl transferase activity in eukaryotes. Nature 1974 1.38
13 Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child. Am J Med Genet 1991 1.24
14 Retroregulation of the int gene of bacteriophage lambda: control of translation completion. Proc Natl Acad Sci U S A 1981 1.20
15 Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia. Blood 1995 1.13
16 Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats. J Med Genet 1998 1.11
17 Inhibitors of macromolecular synthesis in yeast. Methods Cell Biol 1975 1.08
18 Chromosome banding and DNA replication patterns in bird karyotypes. Cytogenet Cell Genet 1989 1.07
19 Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy. J Clin Invest 1990 1.07
20 Physical mapping of the holoprosencephaly critical region on chromosome 7q36. Nat Genet 1993 1.07
21 The relation between well-being, impostor feelings, and gender role orientation among Canadian university students. J Soc Psychol 2001 1.05
22 BrdU-Hoechst flow cytometry: a unique tool for quantitative cell cycle analysis. Exp Cell Res 1988 1.05
23 Endogenous blockage and delay of the chromosome cycle despite normal recruitment and growth phase explain poor proliferation and frequent edomitosis in Fanconi anemia cells. Am J Hum Genet 1985 1.01
24 Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype. J Med Genet 1996 1.01
25 Regulation of the integration-excision reaction by bacteriophage lambda. Cold Spring Harb Symp Quant Biol 1981 1.01
26 Sources of variation in patient response to radiation treatment. Int J Radiat Oncol Biol Phys 2001 0.99
27 Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay. Lab Invest 2001 0.99
28 Measuring neuropsychological change following breast cancer treatment: an analysis of statistical models. J Clin Exp Neuropsychol 2008 0.97
29 Location of sites in human lipocortin I that are phosphorylated by protein tyrosine kinases and protein kinases A and C. Biochemistry 1988 0.97
30 alpha-N-acetylgalactosaminidase deficiency, a new lysosomal storage disorder. J Inherit Metab Dis 1988 0.97
31 Spectral karyotyping of Werner syndrome fibroblast cultures. Cytogenet Cell Genet 2000 0.95
32 Disruption of the FA/BRCA pathway in bladder cancer. Cytogenet Genome Res 2007 0.94
33 Methylation of proteins in 60S ribosomal subunits from Saccharomyces cerevisiae. FEBS Lett 1977 0.93
34 Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. Eur J Hum Genet 2000 0.93
35 A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones. Hum Genet 1993 0.91
36 Isolation and structural characterization of sialic-acid-containing glycopeptides of the O-glycosidic type from the urine of two patients with an hereditary deficiency in alpha-N-acetylgalactosaminidase activity. Biol Chem Hoppe Seyler 1989 0.89
37 Fanconi anemia: causes and consequences of genetic instability. Genome Dyn 2006 0.89
38 Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects. Int J Radiat Oncol Biol Phys 1999 0.89
39 G2 phase cell cycle disturbance as a manifestation of genetic cell damage. Hum Genet 1993 0.89
40 Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia. Mol Syndromol 2012 0.85
41 Cytogenetic studies of skin fibroblast cultures from a karyotypically normal female with dyskeratosis congenita. Clin Genet 1992 0.85
42 Increased incidence of pulmonary tuberculosis in chronic interstitial lung disease. Thorax 1989 0.84
43 Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes. Eur J Pediatr 1992 0.84
44 Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease. Lancet 1987 0.83
45 Increased amount and contour length distribution of small polydisperse circular DNA (spcDNA) in Fanconi anemia. Mutat Res 1993 0.83
46 Hyperparathyroidism associated with Raynaud's phenomenon--a case history. Angiology 1993 0.83
47 Changing pattern of lung tuberculosis. Isr J Med Sci 1986 0.83
48 Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiency. Biochem Biophys Res Commun 1991 0.83
49 BrdU-Hoechst flow cytometry reveals regulation of human lymphocyte growth by donor-age-related growth fraction and transition rate. J Cell Physiol 1985 0.82
50 Localisation of a Fanconi anaemia gene to chromosome 9p. Eur J Hum Genet 1999 0.82
51 Tests of bile-acid and vitamin B12 metabolism in ileal Crohn's disease. Am J Clin Pathol 1980 0.82
52 Bromodeoxyuridine amplifies the inhibitory effect of oxygen on cell proliferation. Cytometry 1988 0.82
53 New mutations in the ataxia telangiectasia gene. Hum Genet 1996 0.81
54 Identification of ataxia telangiectasia heterozygotes, a cancer-prone population, using the single-cell gel electrophoresis (Comet) assay. Lab Invest 1999 0.81
55 The Aspergillus ribonucleolytic toxins (ribotoxins). Targeted Diagn Ther 1992 0.81
56 Long-term survival of patients with chronic obstructive pulmonary disease following mechanical ventilation. Isr J Med Sci 1989 0.81
57 Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly. Hum Genet 1993 0.81
58 The effects of bacterial lipopolysaccharide, anti-receptor antibodies and recombinant interferon on mouse B cell cycle progression using 5-bromo-2'-deoxyuridine/Hoechst 33258 dye flow cytometry. Eur J Immunol 1989 0.80
59 Neuroaxonal dystrophy in infantile alpha-N-acetylgalactosaminidase deficiency. J Neurol Sci 1995 0.80
60 Outcomes of mismatched and unrelated donor hematopoietic stem cell transplantation in Fanconi anemia conditioned with chemotherapy only. Ann Hematol 2015 0.80
61 Factors that contribute to the reduced weight gain following chronic ventromedial hypothalamic stimulation. Behav Brain Res 1994 0.79
62 The substrate for brain-stimulation reward in the lateral preoptic area. II. Connections to the ventral tegmental area. Brain Res 2000 0.79
63 The substrate for brain-stimulation reward in the lateral preoptic area: III. Connections to the lateral hypothalamic area. Behav Neurosci 2001 0.79
64 Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1Q12-32 triplication) via BrdU/Hoechst flow cytometry. Am J Pediatr Hematol Oncol 1987 0.79
65 alpha-N-acetylgalactosaminidase deficiency with mild clinical manifestations and difficult biochemical diagnosis. J Pediatr 1994 0.78
66 siRNA screening identifies differences in the Fanconi anemia pathway in BALB/c-Trp53+/- with susceptibility versus C57BL/6-Trp53+/- mice with resistance to mammary tumors. Oncogene 2013 0.78
67 Degradation of blood group A glycolipid A-6-2 by normal and mutant human skin fibroblasts. J Lipid Res 1998 0.78
68 Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome. Hum Genet 1985 0.78
69 Forebrain neurons driven by rewarding stimulation of the medial forebrain bundle in the rat: comparison of psychophysical and electrophysiological estimates of refractory periods. Brain Res 1989 0.77
70 Structure, origin and effects of a supernumerary marker chromosome 15. Clin Genet 1986 0.77
71 Molecular cloning, structural organization, sequence, chromosomal assignment, and expression of the mouse alpha-N-acetylgalactosaminidase gene. Gene 1998 0.77
72 Modulation of the spontaneous G2 phase blockage in Fanconi anemia cells by caffeine: differences from cells arrested by X-irradiation. Mutat Res 1994 0.77
73 Cell cycle kinetics by BrdU-Hoechst flow cytometry: an alternative to the differential metaphase labelling technique. Cell Tissue Kinet 1985 0.77
74 Epidermal growth factor receptor gene expression in avian epiphyseal growth-plate cartilage cells: effect of serum, parathyroid hormone and atrial natriuretic peptide. Mol Cell Endocrinol 1991 0.77
75 Cell-surface expression of transrearranged Vgamma-cbeta T-cell receptor chains in healthy donors and in ataxia telangiectasia patients. Br J Haematol 2000 0.77
76 Fanconi's anaemia cells have normal steady-state levels and repair of oxidative DNA base modifications sensitive to Fpg protein. Mutat Res 1998 0.76
77 Screening Fanconi anemia lymphoid cell lines of non-A, C, D2, E, F, G subtypes for defects in BRCA2/FANCD1. Cytogenet Genome Res 2003 0.76
78 Presymptomatic diagnosis of Fanconi's anaemia. Lancet 1985 0.76
79 Medial forebrain bundle units in the rat: dependence of refractory period estimates on pulse duration. Behav Brain Res 1991 0.76
80 Screening test for ataxia telangiectasia. Lancet 1987 0.76
81 A heterozygous frameshift mutation in the Fanconi anemia C gene in familial T-ALL and secondary malignancy. Klin Padiatr 2000 0.75
82 Small deletions in the regulatory 3' UTR of the human alpha-tropomyosin gene identified by differential display. Mol Cell Probes 1998 0.75
83 Exploring the role of oxygen in Fanconi's anemia. Recent Results Cancer Res 1997 0.75
84 [Indication status of chromosome analysis in the diagnostic evaluation of recurrent abortions]. Z Geburtshilfe Perinatol 1986 0.75
85 [A combination test for the diagnosis of digestive physiology disorder in regional enteritis]. Verh Dtsch Ges Inn Med 1974 0.75
86 Cerebral glucose metabolism in type I alpha-N-acetylgalactosaminidase deficiency: an infantile neuroaxonal dystrophy. J Child Neurol 1999 0.75
87 [Are there genetic risk factors in the occurrence of choriocarcinoma?]. Geburtshilfe Frauenheilkd 1985 0.75
88 Specific silver staining of experimentally undercondensed chromosome regions. Chromosoma 1984 0.75
89 [Hyperoxaluria in intestinal and liver diseases]. Z Gastroenterol 1977 0.75
90 [A standardized test method for determination of aflatoxin M1 in milk and milk products]. Nahrung 1989 0.75
91 [Holoprosencephaly--clinical picture and genetic counseling in 6 cases]. Klin Padiatr 1985 0.75
92 A variant of Noonan's syndrome: a case history. Angiology 1993 0.75
93 Centromeric association of a microchromosome. A new category of non-random arrangement of metaphase chromosomes. Hum Genet 1989 0.75
94 Sensitivity of bile acid breath test in the diagnosis of bacterial overgrowth in the small intestine with and without the stagnant (blind) loop syndrome. Dig Dis Sci 1979 0.75
95 Patent ductus arteriosus involving three generations--a case history. Angiology 1993 0.75
96 [Severe methemoglobinemia of a nurse after poisoning with the corrosion preventing agent sodium nitrite used in the disinfection of instruments]. Med Welt 1968 0.75
97 Microarray mRNA expression analysis of Fanconi anemia fibroblasts. Cytogenet Genome Res 2008 0.75
98 5-Azacytidine treatments in the characterization of a t(1;21)(q12;q22) carrier karyotype. Clin Genet 1985 0.75
99 The "ruler sign"--a semiquantitative physical sign of chronic obstructive pulmonary disease. Isr J Med Sci 1988 0.75
100 Cytotoxic and genotoxic effects of paclitaxel (Taxol) and radiation in a squamous cell carcinoma cell line of the larynx. Acta Otolaryngol 1998 0.75
101 An investigation into the glycolipid metabolism of alpha-N-acetylgalactosaminidase-deficient fibroblasts using native and artificial glycolipids. Biol Chem Hoppe Seyler 1992 0.75
102 Continuous bromodeoxyuridine labeling and bivariate ethidium bromide/Hoechst flow cytometry in cell kinetics. Cytometry 1989 0.75
103 Pulmonary embolism after short-term treatment of acne vulgaris with ovulation suppressor agents. Med J Aust 1986 0.75
104 [Hyperoxalurin in gastrointestinal and liver diseases]. Verh Dtsch Ges Inn Med 1974 0.75