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Tiemo Grimm

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TOP 3
Tiemo Grimm; Wolfram Kress; Gerhard Meng; Clemens R Müller
Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.
Angelika Stellzig-Eisenhauer; Eva Decker; Philipp Meyer-Marcotty; Christiane Rau; Britta S Fiebig; Wolfram Kress; Kathrin Saar; Franz Rüschendorf; Norbert Hubner; Tiemo Grimm; Emil Witt; Bernhard H F Weber
Primary failure of eruption (PFE)--clinical and molecular genetics analysis.
Ute Felbor; Ulrich Sure; Tiemo Grimm; Helmut Bertalanffy
Genetics of cerebral cavernous angioma.

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All Publications

2012: Tiemo Grimm; Wolfram Kress; Gerhard Meng; Clemens R Müller
Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2012;31(3):179-83.
2010: Angelika Stellzig-Eisenhauer; Eva Decker; Philipp Meyer-Marcotty; Christiane Rau; Britta S Fiebig; Wolfram Kress; Kathrin Saar; Franz Rüschendorf; Norbert Hubner; Tiemo Grimm; Emil Witt; Bernhard H F Weber
Primary failure of eruption (PFE)--clinical and molecular genetics analysis.
Journal of orofacial orthopedics = Fortschritte der Kieferorthopädie : Organ/official journal Deutsche Gesellschaft für Kieferorthopädie 2010;71(1):6-16.
2006: Ute Felbor; Ulrich Sure; Tiemo Grimm; Helmut Bertalanffy
Genetics of cerebral cavernous angioma.
Zentralblatt für Neurochirurgie 2006;67(3):110-6.
2002: Ralf Giess; Bettina Holtmann; Massimiliano Braga; Tiemo Grimm; Bertram Müller-Myhsok; Klaus V Toyka; Michael Sendtner
Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.
American journal of human genetics 2002;70(5):1277-86.
2001: CG Sauer; Karen White; Heidi Stöhr; Tiemo Grimm; A Hutchinson; P S Bernstein; R A Lewis; Francesca Simonelli; Daniel Pauleikhoff; R Allikmets; Bernhard H F Weber
Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration.
The British journal of ophthalmology 2001;85(8):969-75.
2001: Christiane Schneider; Carsten Wessig; Clemens R Müller; Dirk Brechtelsbauer; Tiemo Grimm
Proximal myotonic myopathy and proximal myotonic dystrophy: two different entities? The phenotypic variability of proximal myotonic syndromes.
Neuromuscular disorders : NMD 2001;11(5):485-8.
2000: Christiane Schneider; Tiemo Grimm; Wolfram Kress; Claudia Sommer; Clemens R Müller
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM).
Neuromuscular disorders : NMD 2000;10(7):481-3.
2000: Wolfram Kress; B Mueller-Myhsok; Kenneth Ricker; Christiane Schneider; Manuela C Koch; Klaus V Toyka; CR Mueller; Tiemo Grimm
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).
Neuromuscular disorders : NMD 2000;10(7):478-80.
2000: A Rivera; Karen White; Heidi Stöhr; K Steiner; N Hemmrich; Tiemo Grimm; Bernhard Jurklies; B Lorenz; Hendrik P N Scholl; Eckart Apfelstedt-Sylla; Bernhard H F Weber
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.
American journal of human genetics 2000;67(4):800-13.
2000: Christiane Schneider; A Ziegler; Kenneth Ricker; Tiemo Grimm; Wolfram Kress; C D Reimers; Hans-Michael Meinck; Karlheinz Reiners; Klaus V Toyka
Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.
Neurology 2000;55(3):383-8.
2000: Wolfram Kress; B Petersen; Hartmut Collmann; Tiemo Grimm
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.
Cytogenetics and cell genetics 2000;91(1-4):138-40.
1999: Benjamin Ehmke; Wolfram Kress; Helge Karch; Tiemo Grimm; Bernd Klaiber; Thomas F Flemmig
Interleukin-1 haplotype and periodontal disease progression following therapy.
Journal of clinical periodontology 1999;26(12):810-3.
1999: Markus M Nöthen; Gerd Schulte-Körne; Tiemo Grimm; Sven Cichon; Ina R Vogt; Bertram Müller-Myhsok; Peter Propping; Helmut Remschmidt
Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.
European child & adolescent psychiatry 1999;8 Suppl 3():56-9.
1999: Bertram Müller-Myhsok; Tiemo Grimm
Linkage analysis and genetic models in dyslexia--considerations pertaining to discrete trait analysis and quantitative trait analyses.
European child & adolescent psychiatry 1999;8 Suppl 3():40-2.
1999: Kenneth Ricker; Tiemo Grimm; Manuela C Koch; Christiane Schneider; Wolfram Kress; C D Reimers; Wilhelm Schulte-Mattler; B Mueller-Myhsok; Klaus V Toyka; CR Mueller
Linkage of proximal myotonic myopathy to chromosome 3q.
Neurology 1999;52(1):170-1.
1998: Gerd Schulte-Körne; Tiemo Grimm; Markus M Nöthen; Bertram Müller-Myhsok; Sven Cichon; Ina R Vogt; Peter Propping; Helmut Remschmidt
Evidence for linkage of spelling disability to chromosome 15.
American journal of human genetics 1998;63(1):279-82.
1998: U Hofmann; N Wagner; Tiemo Grimm; Eva-B Bröcker; Henning Hamm
[Linear and whorled nevoid hypermelanosis. Case report and review of the literature].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1998;49(5):408-12.
1997: CG Sauer; H D Schworm; Michael W Ulbig; Anita Blankenagel; Klaus Rohrschneider; Daniel Pauleikhoff; Tiemo Grimm; Bernhard H F Weber
An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1).
Journal of medical genetics 1997;34(12):961-6.
1997: Bertram Müller-Myhsok; H J Heiland; Clemens R Müller; G Meng; Tiemo Grimm; J Ott
Mapping undetected mutations within a gene-evidence for two preferential regions in the DMD gene.
Human heredity 1997;47(2):61-5.
1997: Johannes Oldenburg; Tiemo Grimm; J Becker; K Olek; Hans H Brackmann; Rainer Schwaab
Mutations in severe hemophilia A: distribution within the factor VIII gene, origin and influence on inhibitor development.
Beiträge zur Infusionstherapie und Transfusionsmedizin = Contributions to infusion therapy and transfusion medicine 1997;34():224-30.
1996: J Becker; Rainer Schwaab; A Möller-Taube; U Schwaab; W Schmidt; Hans H Brackmann; Tiemo Grimm; K Olek; Johannes Oldenburg
Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.
American journal of human genetics 1996;58(4):657-70.
1996: Wolfram Kress; Tiemo Grimm; Clemens R Müller; H Keller; R Bittner
Parental source effect on inherited mutations in the dystrophin gene of mice and humans.
Acta geneticae medicae et gemellologiae 1996;45(1-2):251-3.
1995: I Stec; Wolfram Kress; G Meng; B Müller; Clemens R Müller; Tiemo Grimm
Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.
Journal of medical genetics 1995;32(12):930-3.
1995: M Guttenbach; B Koschorz; U Bernthaler; Tiemo Grimm; Michael Schmid
Sex chromosome loss and aging: in situ hybridization studies on human interphase nuclei.
American journal of human genetics 1995;57(5):1143-50.
1995: Volker Schuster; Tiemo Grimm; Wolfram Kress; Silvia Seidenspinner; B H Belohradsky; P Müller; Hans Wolfgang Kreth
[X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies].
Klinische Pädiatrie 1995;207(5):271-6.
1994: Volker Schuster; Silvia Seidenspinner; Tiemo Grimm; Wolfram Kress; S Zielen; M Bock; Hans Wolfgang Kreth
Molecular genetic haplotype segregation studies in three families with X-linked lymphoproliferative disease.
European journal of pediatrics 1994;153(6):432-7.
1994: Tiemo Grimm; G Meng; S Liechti-Gallati; T Bettecken; Clemens R Müller; B Müller
On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.
Journal of medical genetics 1994;31(3):183-6.
1994: S Janocha; Werner Wolz; Stefan Srsen; Klara Srsnova; X Montagutelli; J L Guénet; Tiemo Grimm; Wolfram Kress; Clemens R Müller
The human gene for alkaptonuria (AKU) maps to chromosome 3q.
Genomics 1994;19(1):5-8.
1993: Volker Schuster; Wolfram Kress; W Friedrich; Tiemo Grimm; Hans Wolfgang Kreth
X-linked lymphoproliferative disease. Detection of a paternally inherited mutation in a German family using haplotype analysis.
American journal of diseases of children (1960) 1993;147(12):1303-5.
1993: Johannes Oldenburg; Rainer Schwaab; Tiemo Grimm; Klaus Zerres; P Hakenberg; Hans H Brackmann; K Olek
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.
American journal of human genetics 1993;53(6):1229-38.
1993: Frank Kullmann; Tiemo Grimm
[Holt-Oram syndrome].
Deutsche medizinische Wochenschrift (1946) 1993;118(40):1455-62.
1993: S Schwemmle; K Wolff; L M Palmucci; Tiemo Grimm; Frank Lehmann-Horn; C Hübner; E Hauser; D E Iles; D H MacLennan; Clemens R Müller
Multipoint mapping of the central core disease locus.
Genomics 1993;17(1):205-7.
1993: Frank Kullmann; R Koch; W Feichtinger; H Giesen; M Schmid; Tiemo Grimm
[Holt-Oram syndrome in combination with reciprocal translocation, lung hypoplasia and cardiomyopathy].
Klinische Pädiatrie 1993;205(3):185-9.
1993: Gian Antonio Danieli; F Mioni; C R Müller; libero vitiello; Maria Luisa Mostacciuolo; Tiemo Grimm
Patterns of deletions of the dystrophin gene in different European populations.
Human genetics 1993;91(4):342-6.
1993: A Sander; H Moser; S Liechti-Gallati; Tiemo Grimm; M Zingg; Joram Raveh
Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree.
Human genetics 1993;91(1):55-62.
1991: Manuela C Koch; Kenneth Ricker; M Otto; Tiemo Grimm; K Bender; B Zoll; P S Harper; F Lehmann-Horn; R Rüdel; Eric Hoffman
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.
Human genetics 1991;88(1):71-4.
1991: M Janka; Tiemo Grimm
[Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy].
Klinische Pädiatrie 1991;203(5):354-8.
1991: Manuela C Koch; Kenneth Ricker; M Otto; Tiemo Grimm; Eric Hoffman; R Rüdel; K Bender; B Zoll; P S Harper; F Lehmann-Horn
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17.
Journal of medical genetics 1991;28(9):583-6.
1991: K Kausch; Frank Lehmann-Horn; M Janka; B Wieringa; Tiemo Grimm; Clemens R Müller
Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19.
Genomics 1991;10(3):765-9.
1991: Manuela C Koch; Tiemo Grimm; H G Harley; P S Harper
Genetic risks for children of women with myotonic dystrophy.
American journal of human genetics 1991;48(6):1084-91.
1991: K Kausch; Clemens R Müller; Tiemo Grimm; Kenneth Ricker; Marcella Rietschel; Sabine Rudnik-Schöneborn; K Zerres
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.
Human genetics 1991;86(3):317-8.
1991: S Liechti-Gallati; B Müller; Tiemo Grimm; W Kress; C Müller; E Boltshauser; H Moser; S Braga
X-linked centronuclear myopathy: mapping the gene to Xq28.
Neuromuscular disorders : NMD 1991;1(4):239-45.
1991: Manfred Wehnert; G Machill; Tiemo Grimm; M Janka; R Camman; Winnie Schröder; Falko H Herrmann
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C gene.
Human heredity 1991;41(6):364-9.
1990: Tiemo Grimm; B Müller; Clemens R Müller; M Janka
Theoretical considerations on germline mosaicism in Duchenne muscular dystrophy.
Journal of medical genetics 1990;27(11):683-7.
1989: Tiemo Grimm; B Müller; M Dreier; E Kind; T Bettecken; G Meng; Clemens R Müller
Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene.
American journal of human genetics 1989;45(3):368-72.
1989: B Müller; Maria Luisa Mostacciuolo; Gian Antonio Danieli; Tiemo Grimm
Problems in genetic counseling in a family with an "atypical" centronuclear myopathy.
American journal of medical genetics 1989;32(3):417-9.
1989: M Koch; H Harley; Tiemo Grimm; M Sarfarazi; B Müller; B Zoll; Peter S Harper
Paramyotonia congenita and myotonic dystrophy are not allelic disorders.
Cytogenetics and cell genetics 1989;50(2-3):176-7.
1988: Andreas Gal; Siegfried Uhlhaas; D Glaser; Tiemo Grimm
Prenatal exclusion of Norrie disease with flanking DNA markers.
American journal of medical genetics 1988;31(2):449-53.
1988: Tiemo Grimm; Gian Antonio Danieli; C R Muller
Theoretical expectations for deletional mutations in Duchenne muscular dystrophy.
American journal of medical genetics 1988;29(2):445-51.
1987: J Brandl; Tiemo Grimm
A chromosome supplement to the London Dysmorphology Database.
Journal of medical genetics 1987;24(8):497-8.