| Year |
Citation |
Score |
| 1998 |
Bender K, Beller G, Lautsch S. Tetranucleotide short tandem repeat polymorphisms and their possible mode of origin Cytogenetics and Cell Genetics. 80: 34-36. PMID 9678331 |
0.312 |
|
| 1995 |
Otsen M, Den Bieman M, Winer ES, Jacob HJ, Szpirer J, Szpirer C, Bender K, Van Zutphen LF. Use of simple sequence length polymorphisms for genetic characterization of rat inbred strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 595-601. PMID 8535065 DOI: 10.1007/Bf00352364 |
0.305 |
|
| 1994 |
Bender K, Seibert RT, Wienker TF, Kren V, Pravenec M, Bissbort S. Biochemical genetics of methylglyoxal dehydrogenases in the laboratory rat (Rattus norvegicus) Biochemical Genetics. 32: 147-154. PMID 7993370 DOI: 10.1007/Bf00554618 |
0.346 |
|
| 1991 |
Bender K, Kasulke D, Mayerova A, Hummel K, Weidinger S, Epplen JT, Wienker TF. New mutation versus exclusion at the alpha-1-antitrypsin locus: A multifaceted approach in a problematical paternity case Human Heredity. 41: 1-11. PMID 2050377 DOI: 10.1159/000153966 |
0.31 |
|
| 1991 |
Koch MC, Ricker K, Otto M, Grimm T, Hoffman EP, Rüdel R, Bender K, Zoll B, Harper PS, Lehmann-Horn F. Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17. Journal of Medical Genetics. 28: 583-6. PMID 1683408 DOI: 10.1136/Jmg.28.9.583 |
0.336 |
|
| 1991 |
Koch MC, Ricker K, Otto M, Grimm T, Bender K, Zoll B, Harper PS, Lehmann-Horn F, Rüdel R, Hoffman EP. Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. Human Genetics. 88: 71-4. PMID 1660029 DOI: 10.1007/Bf00204932 |
0.349 |
|
| 1990 |
Bender K, Senff H, Wienker TF, Spiess-Kiefer C, Lehmann-Horn F. A linkage study of malignant hyperthermia (MH) Clinical Genetics. 37: 221-225. PMID 2323092 DOI: 10.1111/J.1399-0004.1990.Tb03506.X |
0.389 |
|
| 1989 |
Steuer M, Mauff G, Adam C, Baur MP, Bender K, Goetz J, Goldmann SF, Hauptmann G, Neugebauer M, Tongio MM, Uring-Lambert B, Wolpl A. An estimate on the frequency of duplicated haplotypes and silent alleles of human C4 protein polymorphism. I. Investigations in healthy Caucasoid families Tissue Antigens. 33: 501-510. PMID 2799804 DOI: 10.1111/J.1399-0039.1989.Tb01701.X |
0.371 |
|
| 1989 |
Geserick G, Mauff G, Siemens I, Waltz H, Mayer A, Bender K, Rose M, Goldmann S, Brenden M, Schröder H. Human BF*F-subtypes: segregation analysis with inclusion of MHC haplotypes Human Genetics. 83: 252-256. PMID 2793168 DOI: 10.1007/Bf00285166 |
0.305 |
|
| 1989 |
Koch M, Harley H, Sarfarazi M, Bender K, Wienker T, Zoll B, Harper PS. Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19 Human Genetics. 82: 163-166. PMID 2722193 DOI: 10.1007/Bf00284051 |
0.402 |
|
| 1988 |
Bissbort S, Hitzeroth HW, du Wentzel DP, Van den Berg CW, Senff H, Wienker TF, Bender K. Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14 Human Genetics. 79: 289-290. PMID 3261272 DOI: 10.1007/Bf00366255 |
0.386 |
|
| 1988 |
Bender K, Bissbort S, Crone H, Senff H, Sleiert A, Neumann H, Koch M, Nagel M, Wienker TF. Linkage relations of JK, CO, KEL and IGK with each other and with AHCY Human Heredity. 38: 12-17. PMID 3127321 DOI: 10.1159/000153747 |
0.323 |
|
| 1987 |
Hamada S, Yamada J, Bender K, Adams M. A new polymorphic pepsinogen locus (Pg-2) in the rat (Rattus norvegicus) Jikken Dobutsu. Experimental Animals. 36: 267-272. PMID 3678371 DOI: 10.1538/Expanim1978.36.3_267 |
0.326 |
|
| 1987 |
Wienker TF, Hudek G, Bissbort S, Mayerová A, Mauff G, Bender K. Linkage studies in a pedigree with Van der Woude syndrome Journal of Medical Genetics. 24: 160-162. PMID 3572998 DOI: 10.1136/Jmg.24.3.160 |
0.385 |
|
| 1987 |
Bender K, Bissbort S, Klein A, Mauff G, Mayerová A, Nagel M, Schilling A, Wienker TF. Coagulation factor XIII: genetic linkage studies with F13B. Genetic Epidemiology. 4: 43-9. PMID 3471677 DOI: 10.1002/Gepi.1370040106 |
0.305 |
|
| 1987 |
Westphal EM, Burmeister M, Wienker TF, Lehrach H, Bender K, Scherer G. Tyrosine aminotransferase and chymotrypsinogen B are linked to haptoglobin on human chromosome 16q: comparison of genetic and physical distances. Genomics. 1: 313-9. PMID 2896626 DOI: 10.1016/0888-7543(87)90030-9 |
0.382 |
|
| 1986 |
Bender K, Bissbort S, Kuhn A, Nagel M, Günther E. Genetic variation of an acid phosphatase (Acp-2) in the laboratory rat: Possible homology with mouse AP-1 and human ACP2 Biochemical Genetics. 24: 1-11. PMID 3964226 DOI: 10.1007/Bf00502974 |
0.367 |
|
| 1986 |
Yamada J, Hamada S, Bender K, Adams M. Linkage studies on 13 biochemical loci and 2 coat color loci in a [(BN x TM) x TM] backcross progeny of the rat (Rattus norvegicus) Jikken Dobutsu. Experimental Animals. 35: 511-515. PMID 3803439 DOI: 10.1538/Expanim1978.35.4_511 |
0.322 |
|
| 1986 |
Apeshiotis F, Bender K. Evidence that S-formylglutathione hydrolase and esterase D polymorphisms are identical Human Genetics. 74: 176-177. PMID 3770745 DOI: 10.1007/Bf00282086 |
0.33 |
|
| 1984 |
Festing MFW, Bender K. Genetic relationships between inbred strains of rats. An analysis based on genetic markers at 28 biochemical loci Genetical Research. 44: 271-281. PMID 6597782 DOI: 10.1017/S0016672300026513 |
0.302 |
|
| 1984 |
Mauff G, Bender K, Giles CM, Goldmann S, Opferkuch W, Wachauf B. Human C4 polymorphism: Pedigree analysis of qualitative, quantiative, and functional parameters as a basis for phenotype interpretations Human Genetics. 65: 362-372. PMID 6420328 DOI: 10.1007/Bf00291561 |
0.357 |
|
| 1983 |
Wieacker P, Wienker TF, Dallapiccola B, Bender K, Davies KE, Ropers HH. Linkage relationships between Retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome. Human Genetics. 64: 143-5. PMID 6885047 DOI: 10.1007/Bf00327111 |
0.542 |
|
| 1983 |
Bender K, Bissbort S, Mayerová A, Mauff G, Wienker TF. C6 linkage studies Journal of Immunogenetics. 10: 61-67. PMID 6841984 DOI: 10.1111/J.1744-313X.1983.Tb01018.X |
0.342 |
|
| 1983 |
Bissbort S, Bender K, Mayerová A, Wienker TF, Mauff G. Genetic linkage relations of the human plasminogen gene Human Genetics. 63: 126-131. PMID 6840757 DOI: 10.1007/Bf00291531 |
0.382 |
|
| 1983 |
Bissbort S, Bender K, Wienker TF, Grzeschik KH. Genetics of human S-adenosylhomocysteine hydrolase. A new polymorphism in man Human Genetics. 65: 68-71. PMID 6580258 DOI: 10.1007/Bf00285031 |
0.428 |
|
| 1982 |
Bender K, Nagel M, Günther E. Es-6, a further polymorphic esterase in the rat Biochemical Genetics. 20: 221-228. PMID 7103927 DOI: 10.1007/Bf00484420 |
0.333 |
|
| 1981 |
Bender K, Cleve H, Guenther E. A previously described serum protein polymorphism in the rat identified as Gc ('vitamin D-binding protein') Animal Blood Groups and Biochemical Genetics. 12: 31-36. PMID 6894673 DOI: 10.1111/J.1365-2052.1981.Tb01528.X |
0.311 |
|
| 1979 |
Bender K, Burckhardt K, Schroetter K. Exclusion of the localization of the Gm, Pi, and C3 genes on 6q25→6qter through blood group analysis of the patients of Schmid, D'Apuzzo and rossi (Hum. Genet. 46, 279-284, 1979) Human Genetics. 53: 129-130. PMID 317067 DOI: 10.1007/Bf00289466 |
0.314 |
|
| 1979 |
Bender K, Müller CR, Schmidt A, Strohmaier U, Wienker TF. Linkage studies on the human Pi, Gm, GLO, and HLA genes Human Genetics. 49: 159-166. PMID 112033 DOI: 10.1007/Bf00277637 |
0.376 |
|
| 1978 |
Bender K, Günther E. Screening of inbred rat strains for electrophoretic protein polymorphisms Biochemical Genetics. 16: 387-398. PMID 736880 DOI: 10.1007/Bf00484206 |
0.368 |
|
| 1978 |
Hiller C, Bischoff M, Schmidt A, Bender K. Analysis of the HLA-ABC linkage disequilibrium: Decreasing strength of gametic association with increasing map distance Human Genetics. 41: 301-312. PMID 649158 DOI: 10.1007/Bf00284764 |
0.393 |
|
| 1977 |
Bender K, Mauff G, Hitzeroth HW. No evidence for linkage disequilibrium between Bf and GLO in African Negroids Human Genetics. 38: 227-230. PMID 908570 DOI: 10.1007/Bf00527407 |
0.414 |
|
| 1977 |
Bender K, Frank R, Hitzeroth HW. Glyoxalase I polymorphism in South African Bantu-speaking Negroids Human Genetics. 38: 223-226. PMID 908569 DOI: 10.1007/Bf00527406 |
0.332 |
|
| 1977 |
Mauff G, Pulverer G, Hummel K, Spielmann W, Bender K. Occurrence of Su in a German family Blut. 34: 357-362. PMID 871535 DOI: 10.1007/Bf00996075 |
0.338 |
|
| 1977 |
Bender K, Mayerová A, Frank R, Hiller C, Wienker T. Haplotype analysis of the linkage group HLA-A:HLA-B:Bf and its bearing on the interpretation of the linkage disequilibrium Human Genetics. 36: 191-196. PMID 858626 DOI: 10.1007/Bf00273257 |
0.324 |
|
| 1977 |
Hitzeroth HW, Bender K, Ropers HH, Geerthsen JM. Tentative evidence for 3--4 haematopoetic stem cells in man. Human Genetics. 35: 175-83. PMID 844863 DOI: 10.1007/Bf00393967 |
0.476 |
|
| 1977 |
Ropers HH, Wienker TF, Grimm T, Schroetter K, Bender K. Evidence for preferential X-chromosome inactivation in a family with Fabry disease. American Journal of Human Genetics. 29: 361-70. PMID 406783 |
0.421 |
|
| 1975 |
Bender K, Frank R. [Esterase D polymorphism: demonstration by high-voltage, starch-gel electrophoresis and presentation of allele frequencies (author's transl)]. Humangenetik. 23: 315-8. PMID 4420151 DOI: 10.1007/Bf00272516 |
0.302 |
|
| 1975 |
Schollen J, Bender K, Deimling Ov. Esterase. XXI. Es-9 , a possibly new polymorphic esterase in Mus musculus genetically linked to Es-2 Biochemical Genetics. 13: 369-377. PMID 1180877 DOI: 10.1007/Bf00485822 |
0.382 |
|
| 1973 |
Engel W, Vogel W, Voiculescu I, Ropers HH, Zenzes MT, Bender K. Cytogenetic and biochemical differences between Apodemus sylvaticus and Apodemus flavicollis, possibly responsible for the failure to interbreed. Comparative Biochemistry and Physiology. B, Comparative Biochemistry. 44: 1165-73. PMID 4736653 DOI: 10.1016/0305-0491(73)90268-X |
0.444 |
|
| 1971 |
Bender K, Schindera F, Kissmeyer-Nielsen F. Localization exclusion of the HL-A genes from the short arm of human chromosome 5. Humangenetik. 11: 78-80. PMID 5490359 DOI: 10.1007/Bf00296309 |
0.357 |
|
| 1971 |
Bender K, Burckhardt K. On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment. Humangenetik. 9: 75-85. PMID 5488998 DOI: 10.1007/Bf00696016 |
0.368 |
|
| 1970 |
Engel W, Bender K, Kadir S, Op't Hof J, Wolf U. [The genetics of 6-PGD (EC; 1.1.1.44) in various mammals. I. Studies on 6 species of Microtinae, Rodentia, Isoenzyme polymorphism and family studies in Microtus oeconomus and Microtus ochrogaster]. Humangenetik. 10: 151-7. PMID 5507049 DOI: 10.1007/Bf00295514 |
0.528 |
|
| 1969 |
Bender K, Reinwein H, Gorman LZ, Wolf U. [Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+]. Humangenetik. 8: 94-104. PMID 5365588 DOI: 10.1007/Bf00295832 |
0.478 |
|
| 1968 |
Wille B, Bender K, Wolf U, Ritter H. [On the population genetics of acid phosphatase in erythrocytes (E C 3.1.3.2.): phenotype and allele frequency in Southwestern Germany]. Humangenetik. 5: 274-7. PMID 5662660 DOI: 10.1007/Bf00281966 |
0.524 |
|
| 1967 |
Bender K, Ritter H, Wolf U. [On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations]. Humangenetik. 4: 85-103. PMID 4865216 DOI: 10.1007/Bf00291253 |
0.547 |
|
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