PubRank

H Starke

Author PubWeight™ 46.06‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation. Cytogenet Genome Res 2006 2.52
2 Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004 2.44
3 Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1. Genes Chromosomes Cancer 2001 1.61
4 Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries. Cytogenet Genome Res 2002 1.39
5 A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH). Hum Genet 2001 1.33
6 Echocardiographic Mimics of aortic root dissection. Chest 1975 1.17
7 Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding. Cytogenet Genome Res 2006 1.15
8 Array painting using microdissected chromosomes to map chromosomal breakpoints. Cytogenet Genome Res 2007 1.11
9 Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB). Cytogenet Cell Genet 2001 1.08
10 [The phenolics of fruits. VIII. Changes in flavonol concentrations during fruit development (authors transl)]. Z Lebensm Unters Forsch 1976 1.06
11 Multicolor FISH probe sets and their applications. Histol Histopathol 2004 1.06
12 Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method. Cytogenet Genome Res 2003 1.04
13 Mitral valve prolapse in anorexia nervosa. Ann Intern Med 1986 0.97
14 Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH. J Med Genet 2000 0.95
15 A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected]. Cytogenet Genome Res 2003 0.94
16 Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure. Hum Reprod 2005 0.93
17 Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient. Cytogenet Genome Res 2005 0.93
18 Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review. J Med Genet 2000 0.93
19 Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay. Am J Med Genet A 2005 0.91
20 Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes. J Med Genet 2002 0.90
21 Left ventricular pseudoaneurysm identified by cross-sectional echocardiography. Ann Intern Med 1979 0.89
22 Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker. Eur J Hum Genet 2001 0.89
23 Evidence for a new microdeletion syndrome in 15q21. Int J Mol Med 2003 0.88
24 Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression. Am J Med Genet 2001 0.88
25 Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenet Genome Res 2006 0.87
26 Upper-limb cardiovascular syndrome. A family study. Am J Cardiol 1967 0.86
27 Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report. J Med Genet 2003 0.86
28 Analysis of non-crossover bivalents in pachytene cells from 10 normal men. Hum Reprod 2006 0.86
29 The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB). Cytogenet Genome Res 2004 0.86
30 Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formation. Cytogenet Genome Res 2003 0.86
31 New insights into the evolution of chromosome 1. Cytogenet Genome Res 2005 0.83
32 Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Cytogenet Genome Res 2005 0.83
33 Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique. Hum Reprod 2005 0.83
34 A molecular cytogenetic study of chromosome evolution in chimpanzee. Cytogenet Genome Res 2006 0.82
35 Incidence and causes of hypokalemia associated with cardiac resuscitation. Am J Emerg Med 1985 0.81
36 De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature. Cytogenet Genome Res 2003 0.81
37 Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenet Genome Res 2006 0.80
38 [Flavonols and flavones of vegetables. VI. On the changes of the flavonols of onions (authors transl)]. Z Lebensm Unters Forsch 1976 0.80
39 FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male. Am J Med Genet A 2004 0.79
40 Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13. Cytogenet Genome Res 2006 0.79
41 Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10]. Am J Med Genet A 2003 0.79
42 Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism. Clin Genet 2003 0.78
43 Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1. Genomics 2001 0.78
44 Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males. Cytogenet Genome Res 2007 0.78
45 Successful pregnancy following Starr-Edwards prosthetic aortic valve replacement. J Kans Med Soc 1967 0.78
46 Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs). Chromosome Res 2004 0.78
47 De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenet Genome Res 2006 0.77
48 Pitfalls of rapid prenatal diagnosis using the interphase nucleus. Prenat Diagn 2001 0.75
49 Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH. Int J Mol Med 1999 0.75
50 Scalar and vectorcardiographic residua of inferior myocardial infarct. J Electrocardiol 1972 0.75
51 Loop logic: an introduction to vectorcardiography. Geriatrics 1975 0.75
52 [Undetected psychiatric disorders in primary health care. A need for psychotherapy]. Cesk Psychiatr 1992 0.75
53 [Ideas for improving lighting of the technical dental work-place]. Zahntechnik (Berl) 1979 0.75
54 [Problems in the formation of social relations between dentists and patients]. Stomatol DDR 1984 0.75
55 [On the method of social psychiatric family investigations]. Nervenarzt 1967 0.75
56 Diuretic-induced hypokalemia: a possible cause of out-of-hospital cardiac arrest. Nebr Med J 1985 0.75
57 Transposition; diagnosis and operative management of corrected transposition of the great vessels. J Kans Med Soc 1969 0.75
58 [Use of covariance selection in the analysis of psychosocial symptom complexes]. Z Gesamte Hyg 1983 0.75
59 Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype. J Med Genet 2002 0.75
60 [Experiences with group discussion in the psychiatric station]. Z Arztl Fortbild (Jena) 1967 0.75
61 Spurious ST segment abnormalities caused by atrial repolarization. Nebr Med J 1979 0.75
62 Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21. Clin Genet 2001 0.75
63 [Laboratory experiments of study the activation and performance behavior of normal persons and of persons suffering from nervous disturbances]. Z Gesamte Hyg 1979 0.75
64 [Some problems of epidemiologic research in psychosocial diseases]. Z Gesamte Hyg 1983 0.75
65 Mechanism of disappearance of S3 with maturation. Am J Cardiol 1989 0.75
66 [Importance of social relation structures in psychoses and post-psychotic rehabilitation]. Z Arztl Fortbild (Jena) 1970 0.75
67 Intermittent complete atrioventricular block masquerading as epilepsy in the mitral valve prolapse syndrome. Chest 1977 0.75
68 [Flavonols and flavones of vegetables. VII. Flavonols of leek, chive and garlic (author's transl)]. Z Lebensm Unters Forsch 1976 0.75
69 Pacemakers. Experience with epicardial and transvenous pacemakers. J Kans Med Soc 1970 0.75
70 Leaflet to left ventricular size disproportion and prolapse of a structurally normal mitral valve in anorexia nervosa. Am J Cardiol 1987 0.75
71 Exercise stress testing. Geriatrics 1975 0.75
72 Echocardiographic diagnosis of silent mitral stenosis. Nebr Med J 1975 0.75
73 [Problems in the planning and implementation of a study of the determination of psychotherapy needs]. Z Gesamte Hyg 1982 0.75
74 [Studies on the effect of assembly-belt work on the health status of workers at a national enterprise]. Dtsch Gesundheitsw 1968 0.75
75 [Diagnosis of psychosocial disorders based on a complaint questionnaire]. Z Gesamte Hyg 1984 0.75
76 [Multidimensional therapy of vasoautonomic disorders]. Psychiatr Neurol Med Psychol Beih 1966 0.75
77 Bronchopulmonary arterial communications in pulmonary atresia with ventricular septal defect. Am J Cardiol 1969 0.75
78 [Autogenic training within the therapeutic scope of schizophrenic patients]. Psychiatr Neurol Med Psychol (Leipz) 1976 0.75