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Horst Ritter - Publications

Affiliations: 
Anthropology and Human genetics Eberhard Karls Universität Tübingen, Tübingen, Baden-Württemberg, Germany 
Area:
Human genetics
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74 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
1998 Pöltl R, Luckenbach C, Hixson J, Ritter H. The short tandem repeat loci hTPO, THO1 and FGA Human Heredity. 48: 318-324. PMID 9813453 DOI: 10.1159/000022823  0.338
1998 Momhinweg E, Luckenbach C, Fimmers R, Ritter H. D3S1358: Sequence analysis and gene frequency in a German population Forensic Science International. 95: 173-178. PMID 9722979 DOI: 10.1016/S0379-0738(98)00096-6  0.332
1998 Pöltl R, Luckenbach C, Ritter H. The short tandem repeat locus D3S1359 Forensic Science International. 95: 163-168. PMID 9722977 DOI: 10.1016/S0379-0738(98)00087-5  0.338
1996 Pöltl R, Luckenbach C, Reinhold J, Fimmers R, Ritter H. Comparison of German population data on the apoB-HVR locus with other Caucasian, Asian and Black populations Forensic Science International. 80: 221-227. PMID 8682422 DOI: 10.1016/0379-0738(96)01917-2  0.318
1995 Arnold G, Kloor D, Kömpf J, Ritter H. Subtyping of coagulation factor XIIIA Human Heredity. 45: 319-322. PMID 8537079 DOI: 10.1159/000154300  0.305
1995 Durr C, Hinney A, Luckenbach C, Ritter H. Detection of two hypervariable (ATTTT)n loci in the human genome Electrophoresis. 16: 719-721. PMID 7588550 DOI: 10.1002/Elps.11501601116  0.336
1995 Blin N, Kaiser P, Krone W, Ritter H, Rosing-Diederich I, Schroeder-Kurth TM, Vogel W, Wolf U. Assignment, structure and development of the Institute for Human Genetics (and Anthropology) of the Universities in Baden-Wurttemberg | AUFGABEN, STRUKTUR UND ENTWICKLUNG DER INSTITUTE FUR HUMANGENETIK (UND ANTHROPOLOGIE) AN DEN UNIVERSITATEN IN BADEN-WURTTEMBERG Medizinische Genetik. 7: 14-18.  0.469
1993 Krczal D, Ritter H, Kömpf J. Polymorphism of glucose dehydrogenase (GDH, EC 1.1.1.47): formal and population genetic data Human Genetics. 91: 290-292. PMID 8478014 DOI: 10.1007/Bf00218276  0.371
1992 Dürr C, Hinney A, Luckenbach C, Kömpf J, Ritter H. Genetic studies of antithrombin III with IEF and ASO hybridization Human Genetics. 90: 457-459. PMID 1483705 DOI: 10.1007/Bf00220477  0.368
1991 Rocha J, Kompf J, Ferrand N, Amorim A, Ritter H. Separation of human alloalbumin variants by isoelectric focusing Electrophoresis. 12: 313-314. PMID 1906401 DOI: 10.1002/Elps.1150120415  0.32
1991 Luckenbach C, Kömpf J, Ritter H. Genetic polymorphism of inter-alpha-trypsin-inhibitor (ITI): Formal genetic and linkage analyses Human Genetics. 87: 89-90. PMID 1709912 DOI: 10.1007/Bf01213100  0.394
1991 Ritter H. On the statistics of the "genetic fingerprint" International Journal of Legal Medicine. 104: 307-308. PMID 1685896 DOI: 10.1007/Bf01369592  0.302
1990 Luckenbach C, Kömpf J, Ritter H. Genetic studies on human thyroxine-binding globulin (TBG) Human Genetics. 84: 368-370. PMID 2106478 DOI: 10.1007/Bf00196237  0.346
1989 Kömpf J, Ritter H, Lisch W, Weidle EG, Baur MP. Linkage analysis in granular corneal dystrophy (Groenouw I), Schnyder's crystalline corneal dystrophy, and Reis-Bücklers' corneal dystrophy Graefe's Archive For Clinical and Experimental Ophthalmology. 227: 538-540. PMID 2625210 DOI: 10.1007/Bf02169448  0.332
1988 Amorim A, Rocha J, Kompf J, Ritter H. Formal genetics of esterase D (EC 3.1.1.1): Evidence for a sex-phenotype association Human Heredity. 38: 255-257. PMID 3169802 DOI: 10.1159/000153794  0.348
1988 Kömpf J, Luckenbach C, Kloor D, Schunter F, Wernet P, Ritter H. Human factor H (β1H-globulin): linkage analysis Human Genetics. 79: 181-182. PMID 2968949 DOI: 10.1007/Bf00280562  0.338
1985 Kömpf J, Schunter F, Wernet P, Ritter H. Linkage between the loci for mitochondrial malic enzyme (ME2) and coagulation factor XIIIA subunit (F13A) Human Genetics. 70: 43-44. PMID 2860058 DOI: 10.1007/Bf00389457  0.329
1982 Amorim A, Kömpf J, Schunter F, Ritter H. Aminolevulinate dehydratase (E.C. 4.2.1.24): Linkage analysis Human Genetics. 61: 48-49. PMID 6957372 DOI: 10.1007/Bf00291331  0.366
1980 Kömpf J, Siebert G, Ritter H, Heilbronner H, Schunter F, Wernet P, Gupta D, Moeller H. Data on linkage relations between GLO and 21-hydroxylase Human Genetics. 54: 419-420. PMID 6967447 DOI: 10.1007/Bf00291592  0.318
1980 Siebert G, Kömpf J, Ritter H. Galactose-1-phosphate-uridyltransferase (E.C.2.7.7.11): A simple routine method for detecting individuals heterozygous for the silent allele Gt0 Human Genetics. 54: 273-275. PMID 6248450 DOI: 10.1007/Bf00278984  0.301
1980 Amorim A, Siebert G, Ritter H, Kömpf J. Formal genetics of phosphoglycolate phosphatase (PGP): Investigation on 272 mother-child pairs Human Genetics. 53: 419-420. PMID 6246002 DOI: 10.1007/Bf00287066  0.352
1979 Ritter H, Kömpf J. Human mitochondrial glutamic-oxaloacetic-transaminase, GOTM: Formal genetics Human Genetics. 51: 327-329. PMID 511164 DOI: 10.1007/Bf00283403  0.36
1979 Kömpf J, Siebert G, Ritter H. Common polymorphism of peptidase A: Formal genetics and population data Human Genetics. 51: 323-325. PMID 511163 DOI: 10.1007/Bf00283402  0.369
1979 Siebert G, Ritter H, Koempf J. Mitochondrial malic enzyme (E.C. 1.1.1.40) in human leukocytes: Formal genetics and population genetics Human Genetics. 51: 319-322. PMID 511162 DOI: 10.1007/Bf00283401  0.401
1979 Kömpf J, Ritter H. Polymorphism of alanine aminotransferase (E.C.2.7.6.1): Common and rare alleles Human Genetics. 51: 287-292. PMID 511157 DOI: 10.1007/Bf00283396  0.334
1979 Kömpf J, Siebert G, Ritter H. Human pancreatic amylase polymorphism: Formal genetics and population genetics Human Genetics. 51: 217-220. PMID 315910 DOI: 10.1007/Bf00287179  0.424
1978 Friedrichson U, Ritter H, Schmitt J. Genetic variation of aldehyde dehydrogenase in primates Folia Primatologica. 29: 95-97. PMID 95997 DOI: 10.1159/000155831  0.319
1976 Mayr WR, Mayr D, Kömpf J, Bissbort S, Ritter H. Possible linkage of HL-A and GLO Human Genetics. 31: 241-242. PMID 1248833 DOI: 10.1007/Bf00296153  0.308
1975 Kömpf J, Bissbort S, Ritter H. Red cell glyoxalase I (E.C.: 4.4.1.5): Formal genetics and linkage relations Human Genetics. 28: 249-251. PMID 1150284 DOI: 10.1007/Bf00278552  0.389
1975 Bissbort S, Kömpf J, Ritter H. Evidence for linkage between the loci of PGM3 and MNSs Human Genetics. 28: 245-247. PMID 1150283 DOI: 10.1007/Bf00278551  0.309
1975 Kömpf J, Bissbort S, Gussmann S, Ritter H. Polymorphism of red cell glyoxalase I (E.C.: 4.4.1.5). A new genetic marker in man - Investigation of 169 mother-child combinations Human Genetics. 27: 141-143. PMID 1150236 DOI: 10.1007/Bf00273329  0.38
1975 Friedrichson U, Reichel K, Ritter H, Schmitt J. Genetic variation of red cell nucleoside phosphorylase in primates Human Genetics. 28: 253-254. PMID 807517 DOI: 10.1007/Bf00278553  0.37
1974 Ritter H, Schmitt J. Mannose phosphate isomerase: Additional variants in primates Human Genetics. 21: 97-98. PMID 4210014 DOI: 10.1007/Bf00278574  0.319
1974 Ritter H, Schmitt J. Interspecific variability of red cell phosphoglycerate kinase in primates Human Genetics. 21: 93-96. PMID 4209787 DOI: 10.1007/Bf00278573  0.341
1974 Schmitt J, Ritter H. Interspecific variability of soluble isocitrate dehydrogenase in primates Human Genetics. 21: 89-92. PMID 4152143 DOI: 10.1007/Bf00278572  0.39
1974 Ritter H, Friedrichson U, Schmitt J. Genetic polymorphism of hexokinase in primates Human Genetics. 22: 265-266. DOI: 10.1007/Bf00284834  0.408
1974 Schmitt J, Ritter H. Genetic variation of aconitate hydratase in man Humangenetik. 22: 263-264. DOI: 10.1007/Bf00284833  0.386
1974 Ritter H, Friedrichson U, Schmitt J. Genetic variation of mannose phosphate isomerase in man Human Genetics. 22: 261. DOI: 10.1007/Bf00284832  0.391
1973 Ritter H, Schmitt J. Genetic polymorphism of liver esterases in primates. I. Papio cynocephalus (Linnaeus, 1766) Humangenetik. 19: 335-336. PMID 4202880 DOI: 10.1007/Bf00278414  0.358
1973 Schmitt J, Ritter H. Genetic polymorphism of Isocitrate dehydrogenase in Primates Human Genetics. 19: 327-329. PMID 4202878 DOI: 10.1007/Bf00278412  0.392
1973 Ritter H, Schmitt J. Genetic polymorphism of mannosephosphate isomerase in primates Humangenetik. 19: 325-326. PMID 4202877 DOI: 10.1007/Bf00278411  0.408
1972 Kömpf J, Ritter H, Schmitt J. Genetic polymorphism of glycerol-3-phosphate dehydrogenase (E.C.: 1.1.1.8). I. Transspecific variability of G-3-PD subunit B in Primates. Humangenetik. 13: 75-7. PMID 5000537 DOI: 10.1007/Bf00446420  0.329
1972 Kömpf J, Ritter H, Schmitt J. Genetic polymorphism of glycerol-3-phosphate dehydrogenase (E.C.: 1.1.1.8) - II. Transspecific variability of G-3-PD subunit A in primates. Formal genetics and population genetics Humangenetik. 14: 103-106. PMID 4623757 DOI: 10.1007/Bf00273292  0.397
1972 Kömpf J, Ritter H, Schmitt J. Transspecific variability of D-fructose-1,6-diphosphate-1-phospholhydrolase (e.c.: 3.1.3.11) in Primates. Humangenetik. 14: 64-5. PMID 4335712 DOI: 10.1007/Bf00273034  0.345
1972 Schmitt J, Kömpf J, Ritter H. Transspecific variability of mitochondrial NAD-malate dehydrogenase (E.C.: 1.1.1.37) in Primates. Humangenetik. 13: 69-71. PMID 4329954 DOI: 10.1007/Bf00446418  0.333
1971 Ritter H, Tariverdian G, Arnold H, Blume KG, Schröter W, Zimmerschitt E, Brittinger G, König E, Wendt GG. Evidence for linkage between the locus for the ABO-system and the locus for phosphoglucoseisomerase (PGI). Humangenetik. 11: 349-50. PMID 5550600 DOI: 10.1007/Bf00278666  0.337
1971 Ritter H, Wendt GG, Tariverdian G, Zilch J, Rube M, Kirchberg G. Genetics and linkage analysis of adenosine deaminase. Humangenetik. 14: 69-71. PMID 5144905 DOI: 10.1007/Bf00273036  0.396
1971 Ritter H, Wendt GG. Population genetics of phosphoglucose isomerase (EC:5.3.1.9). Humangenetik. 13: 356-7. PMID 5135857 DOI: 10.1007/Bf00273957  0.372
1971 Ritter H, Wendt GG, Zilch I, Kömpf J, Cramer H, Kirchberg G. Genetics and linkage analysis for the acid phosphatase of the erythrocytes. Humangenetik. 13: 353-5. PMID 5135856 DOI: 10.1007/Bf00273956  0.366
1971 Wendt GG, Ritter H, Zilch I, Tariverdian G, Utermann G, Kindermann I, Kirchberg G. Genetics and linkage analysis on phosphoglucomutase. Humangenetik. 13: 350-2. PMID 5135855 DOI: 10.1007/Bf00273955  0.32
1971 Wendt GG, Ritter H, Zilch I, Tariverdian G, Kindermann I, Kirchberg G. Genetics and linkage analysis on adenylate kinase. Humangenetik. 13: 347-9. PMID 5135854 DOI: 10.1007/Bf00273954  0.358
1971 Ritter H, Tariverdian G, Wendt GG, Zilch I. Genetic and linkage analysis on 6-PGD. Humangenetik. 14: 73-5. PMID 5004219 DOI: 10.1007/Bf00273038  0.404
1971 Kömpf J, Ritter H, Schmitt J. Transspecific variability of glutamic oxaloacetic transaminase (E.C. 2.6.1.1) in Primates. Human Genetics. 13: 72-74. PMID 5000536 DOI: 10.1007/Bf00446419  0.334
1971 Tariverdian G, Ritter H, Schmitt J. Transspecific variability of phosphohexose isomerase (E. C.: 5. 3. 1. 9) in primates Human Genetics. 12: 105-109. PMID 4998684 DOI: 10.1007/Bf00291465  0.33
1970 Tariverdian G, Ritter H, Wendt GG. [Genetically determined variants of NADH-diaphorase]. Humangenetik. 11: 75-7. PMID 4321430 DOI: 10.1007/Bf00296308  0.393
1969 Wille B, Ritter H. [The formal genetics of adenylate kinase (EC: 2.7.4.3); evidence for linkage between the loci for AK and ABO]. Humangenetik. 7: 263-4. PMID 5800710 DOI: 10.1007/Bf00273180  0.366
1969 Klose J, Wolf U, Hitzeroth H, Ritter H, Ohno S. Polyploidization in the fish family Cyprinidae, order Cypriniformes - II. Duplication of the gene loci coding for lactate dehydrogenase (E.C.: 1.1.1.27) and 6-phosphogluconate dehydrogenase (E.C.: 1.1.1.44) in various species of Cyprinidae Human Genetics. 7: 245-250. PMID 5800706 DOI: 10.1007/BF00273174  0.439
1969 Ritter H, Baitsch H, Wolf U. [On the formal genetics of isoenzymes, using 6-PGD (EC:1.1.1.44) as an example]. Humangenetik. 7: 1-4. PMID 5770376 DOI: 10.1007/BF00278686  0.688
1969 Ropers H, Ritter H. Zur formalen Genetik der 6-Phosphogluconatdehydrogenasen (EC: 1.1.1.44); Untersuchung von 220 Familien Human Genetics. 8. DOI: 10.1007/Bf00286760  0.353
1969 Wille B, Schmidt E, Ritter H. Zur formalen Genetik der Phosphoglucomutasen (EC: 2.7.5.1); Untersuchung von 366 Familien Human Genetics. 8. DOI: 10.1007/Bf00286759  0.336
1968 Engel W, Reinwein H, Bombel D, Ritter H, Wolf U. Multiple malformations in a girl of karyotype 46, XY, 17q+ | Multiple Mißbildungen bei einem Mädchen mit dem Karyotypus 46, XY, 17q+ Human Genetics. 6: 311-325. PMID 5713617 DOI: 10.1007/BF00286800  0.398
1968 Engel W, Op't Hof J, Ritter H, Wolf U. Mapping of human chromosomes - II. Exclusion of gene loci in deficiency 5p | Zur Frage der Zuordnung von Loci - II. Lokalisierungsausschlüsse bei Defizienzen 5p Human Genetics. 6: 279-280. PMID 5709088 DOI: 10.1007/Bf00291874  0.491
1968 Böckelmann W, Wolf U, Ritter H. Polymorphism of the phosphotransferases adenylate kinase and pyruvate kinase - Existence of a common subunit? Human Genetics. 6: 78-83. PMID 5699898 DOI: 10.1007/BF00287158  0.425
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  0.494
1968 Klose J, Wolf U, Hitzeroth H, Ritter H, Atkin NB, Ohno S. Duplication of the LDH gene loci by polyploidization in the fish order Clupeiformes Human Genetics. 5: 190-196. PMID 5662651 DOI: 10.1007/BF00281954  0.438
1968 Reinwein H, Ritter H, Wolf U. Deletion of short arm of a chromosome 18 (46, XX, 18 p-). Humangenetik. 5: 72-3. PMID 5585063 DOI: 10.1007/BF00286215  0.396
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  0.463
1966 Reinwein H, Schilli W, Ritter H, Brehme H, Wolf U. [Studies on a family with orofaciodigital syndrome]. Humangenetik. 2: 165-77. PMID 5916636 DOI: 10.1007/BF00291516  0.411
1964 GOEDDE HW, RITTER H, OMOTO K, BAITSCH H. [ON FORMAL GENETICS OF PSUDOCHOLINESTERASE. STUDIES ON 408 FAMILIES]. Humangenetik. 1: 1-13. PMID 14338380  0.629
1964 RITTER H, ROPARTZ C, BAITSCH H, ROUSSEAU PY, RIVAT L, REMY K. [ON THE MORPHOLOGY AND GENETICS OF GM POLYMORPHISM OF GAMMA GLOBULINS (CHARACTERISTICS OF GM(A), GM(B), GM(E); STUDY ON 387 FAMILIES]. Acta Genetica Et Statistica Medica. 14: 4-14. PMID 14159878  0.633
1964 ROPARTZ C, ROUSSEAU PY, RIVAT L, BAITSCH H, RITTER H, PINKERTON FJ, MERMOD LE. [GAMMA GLOBULIN GROUPS GM AND INV AMONG THE POPULATION OF HONOLULU (HAWAII)]. Acta Genetica Et Statistica Medica. 14: 25-35. PMID 14159875  0.552
1964 Goedde HW, Omoto K, Ritter H, Baitsch H. Zur formalen Genetik der Pseudocholinesterasen - Untersuchung von 408 Familien Human Genetics. 1: 1-13. DOI: 10.1007/BF00289360  0.538
1963 BAITSCH H, RITTER H, GOEDDE HW, ALTLAND K. [ON GENETICS OF SERUM PROTEINS: HP-SERUM GROUPS, GC-FACTOR, GM-SERUM GROUPS AND PSEUDOCHOLINESTERASE VARIANTS IN EUROPEAN POPULATIONS]. Vox Sanguinis. 8: 594-604. PMID 14067361 DOI: 10.1111/j.1423-0410.1963.tb04187.x  0.596
1963 BAITSCH H, RITTER H. [STUDIES ON THE GENETICS OF SERUM PROTEINS: THE GC FACTOR OF HIRSCHFELD AND ITS ALLELE INCIDENCE IN SOUTHWESTERN GERMANY]. Blut. 9: 278-83. PMID 14047330 DOI: 10.1007/BF01678991  0.623
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