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Gerd Utermann

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TOP 3
Florian Kronenberg; Gerd Utermann
Lipoprotein(a): resurrected by genetics.
Anne Frühmesser; Edda Haberlandt; Werner Judmaier; Albert Schinzel; Barbara Utermann; Gerd Utermann; Johannes Zschocke; Martin Erdel; Christine Fauth; Dieter Kotzot
Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype.
Angela M Hancock; David B Witonsky; Gorka Alkorta-Aranburu; Cynthia M Beall; Amha Gebremedhin; Rem Sukernik; Gerd Utermann; Jonathan K Pritchard; Graham Coop; Anna Di Rienzo
Adaptations to climate-mediated selective pressures in humans.

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All Publications

2013: Florian Kronenberg; Gerd Utermann
Lipoprotein(a): resurrected by genetics.
Journal of internal medicine 2013;273(1):6-30.
2012: Anne Frühmesser; Edda Haberlandt; Werner Judmaier; Albert Schinzel; Barbara Utermann; Gerd Utermann; Johannes Zschocke; Martin Erdel; Christine Fauth; Dieter Kotzot
Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype.
American journal of medical genetics. Part A 2012;158A(9):2239-44.
2011: Angela M Hancock; David B Witonsky; Gorka Alkorta-Aranburu; Cynthia M Beall; Amha Gebremedhin; Rem Sukernik; Gerd Utermann; Jonathan K Pritchard; Graham Coop; Anna Di Rienzo
Adaptations to climate-mediated selective pressures in humans.
PLoS genetics 2011;7(4):e1001375.
2010: V Grossmann; M Höckner; H Karmous-Benailly; Desheng Liang; R Puttinger; R Quadrelli; B Röthlisberger; A Huber; L Wu; A Spreiz; Christine Fauth; Martin Erdel; J Zschocke; Gerd Utermann; Dieter Kotzot
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis.
Clinical genetics 2010;78(6):548-53.
2010: Ana Spreiz; Doris Müller; Sibylle Zotter; Ursula Albrecht; Matthias Baumann; Christine Fauth; Martin Erdel; Johannes Zschocke; Gerd Utermann; Dieter Kotzot
Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21).
American journal of medical genetics. Part A 2010;152A(11):2762-7.
2010: Peter Clayton; Ilja Demuth; Björn Fischer; Sophia Gravemann; Sevjidmaa Baasanjav; Katja Brossuleit; Mohsen Karbasyian; Moritz Kieslich; Christine Lang; Anuska Mann; Sahar Mansour; Stefan Mundlos; Eva Rossier; Nele Schnipper; Karl Sperling; Sigmar Stricker; Gerd Utermann; Amparo Vaya; Markus Veen; Monika Zwerger; Katrin Hoffmann
Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.
Nucleus (Austin, Tex.) 2010;1(4):354-66.
2010: Franz Binkert; Ana Spreiz; Martina Höckner; Peter Miny; Brigitte von Dach Leu; Martin Erdel; Johannes Zschocke; Gerd Utermann; Dieter Kotzot
Parental origin and mechanism of formation of a 46,X,der(X)(pter-->q21.1::p11.4-->pter)/45,X karyotype in a woman with mild Turner syndrome.
Fertility and sterility 2010;94(1):350.e12-5.
2010: Angela M Hancock; David B Witonsky; Edvard Ehler; Gorka Alkorta-Aranburu; Cynthia Beall; Amha Gebremedhin; Rem Sukernik; Gerd Utermann; Jonathan Pritchard; Graham Coop; Anna Di Rienzo
Colloquium paper: human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency.
Proceedings of the National Academy of Sciences of the United States of America 2010;107 Suppl 2():8924-30.
2010: Frank M Ruemmele; Thomas Müller; Natalia Schiefermeier; Hannes L Ebner; Silvia Lechner; Kristian Pfaller; Cornelia E Thöni; Olivier Goulet; Florence Lacaille; Jacques Schmitz; Virginie Colomb; Frédérique Sauvat; Yann Revillon; Danielle Canioni; Nicole Brousse; Genevieve de Saint-Basile; Juliette Lefebvre; Peter Heinz-Erian; Axel Enninger; Gerd Utermann; Michael W Hess; Andreas R Janecke; Lukas A Huber
Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model.
Human mutation 2010;31(5):544-51.
2010: Hans Georg Kraft; Florian Kronenberg; Gerd Utermann
Genetic variants in Lp(a) lipoprotein and coronary disease.
The New England journal of medicine 2010;362(12):1146; author reply 1147-8.
2010: Michael Pampel; Sandra Maier; Alfons Kreczy; Helga Weirich-Schwaiger; Gerd Utermann; Andreas R Janecke
Refinement of the GINGF3 locus for hereditary gingival fibromatosis.
European journal of pediatrics 2010;169(3):327-32.
2009: Munis Dündar; Thomas Müller; Qi Zhang; Jing Pan; Beat Steinmann; Julia Vodopiutz; Robert Gruber; Tohru Sonoda; Birgit Krabichler; Gerd Utermann; Jacques U Baenziger; Lijuan Zhang; Andreas R Janecke
Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome.
American journal of human genetics 2009;85(6):873-82.
2009: Vera Grossmann; Doris Müller; Wilfried Müller; Friedrich Fresser; Martin Erdel; Andreas R Janecke; Johannes Zschocke; Gerd Utermann; Dieter Kotzot
"Essentially" pure trisomy 3q27 --> qter: further delineation of the partial trisomy 3q phenotype.
American journal of medical genetics. Part A 2009;149A(11):2522-6.
2009: Gabriel Miltenberger-Miltenyi; Thomas Schwarzbraun; Wolfgang N Löscher; Julia Wanschitz; Christian Windpassinger; Hans-Christoph Duba; Rainer Seidl; Gerhard Albrecht; Helga Weirich-Schwaiger; Heinz Zoller; Gerd Utermann; Michaela Auer-Grumbach; Andreas R Janecke
Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations.
European journal of human genetics : EJHG 2009;17(9):1154-9.
2009: Beate R Jaeger; Yvonne Richter; Dorothea Nagel; Franz Heigl; Anja Vogt; Eberhard Roeseler; Klaus Parhofer; Wolfgang Ramlow; Michael Koch; Gerd Utermann; Carlos A Labarrere; Dietrich Seidel
Longitudinal cohort study on the effectiveness of lipid apheresis treatment to reduce high lipoprotein(a) levels and prevent major adverse coronary events.
Nature clinical practice. Cardiovascular medicine 2009;6(3):229-39.
2009: Peter Heinz-Erian; Thomas Müller; Birgit Krabichler; Melanie Schranz; Christian Becker; Franz Rüschendorf; Peter Nürnberg; Bernard Rossier; Mihailo Vujic; Ian W Booth; Christer Holmberg; Cisca Wijmenga; Giedre Grigelioniene; C M Frank Kneepkens; Stefan Rosipal; Martin Mistrik; Matthias Kappler; Laurent Michaud; Ludwig-Christoph Dóczy; Victoria Mok Siu; Marie Krantz; Heinz Zoller; Gerd Utermann; Andreas R Janecke
Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea.
American journal of human genetics 2009;84(2):188-96.
2008: Thomas Müller; Michael W Hess; Natalia Schiefermeier; Kristian Pfaller; Hannes L Ebner; Peter Heinz-Erian; Hannes Ponstingl; Joachim Partsch; Barbara Röllinghoff; Henrik Köhler; Thomas Berger; Henning Lenhartz; Barbara Schlenck; Roderick J Houwen; Christopher J Taylor; Heinz Zoller; Silvia Lechner; Olivier Goulet; Gerd Utermann; Frank M Ruemmele; Lukas A Huber; Andreas R Janecke
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.
Nature genetics 2008;40(10):1163-5.
2008: Martina Höckner; Barbara Utermann; Martin Erdel; Christine Fauth; Gerd Utermann; Dieter Kotzot
Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman.
American journal of medical genetics. Part A 2008;146(7):925-9.
2008: Martina Witsch-Baumgartner; Ilona Schwentner; M Gruber; P Benlian; Jaume Bertranpetit; E Bieth; F Chevy; N Clusellas; X Estivill; G Gasparini; M Giros; Richard I Kelley; Malgorzata Krajewska-Walasek; J Menzel; T Miettinen; M Ogorelkova; M Rossi; I Scala; Albert Schinzel; K Schmidt; D Schönitzer; E Seemanova; K Sperling; M Syrrou; P J Talmud; B Wollnik; M Krawczak; D Labuda; Gerd Utermann
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.
Journal of medical genetics 2008;45(4):200-9.
2007: Vania Yotova; Jean-François Lefebvre; Oleksiy Kohany; Jerzy Jurka; Roman Michalski; David Modiano; Gerd Utermann; scott williams; Damian Labuda
Tracing genetic history of modern humans using X-chromosome lineages.
Human genetics 2007;122(5):431-43.
2007: Veit Schoenborn; Henning Gohlke; Iris M Heid; Thomas Illig; Gerd Utermann; Florian Kronenberg
Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: to separate the wheat from the chaff.
Human mutation 2007;28(11):1141-9.
2007: Andreas Schuster; Andreas R Janecke; Robert Wilke; Eduard Schmid; Debra A Thompson; Gerd Utermann; Bernd Wissinger; Eberhart Zrenner; Andreas Gal
The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.
Investigative ophthalmology & visual science 2007;48(4):1824-31.
2007: Robert Gruber; Andreas R Janecke; Christine Fauth; Gerd Utermann; Peter O Fritsch; Matthias Schmuth
Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris.
European journal of human genetics : EJHG 2007;15(2):179-84.
2006: Eduard Schmid; Walter Lisch; Wolfgang Philipp; Silvia Lechner; Wolfgang Göttinger; Ursula Schlötzer-Schrehardt; Thomas Müller; Gerd Utermann; Andreas R Janecke
A new, X-linked endothelial corneal dystrophy.
American journal of ophthalmology 2006;141(3):478-487.
2006: Edda Haberlandt; Christine Svejda; Stephan Felber; Sara Baumgartner; Barbara Günther; Gerd Utermann; Dieter Kotzot
Yellow teeth, seizures, and mental retardation: a less severe case of Kohlschütter-Tönz syndrome.
American journal of medical genetics. Part A 2006;140(3):281-3.
2006: Konrad Schmidt; Hans Georg Kraft; Walther Parson; Gerd Utermann
Genetics of the Lp(a)/apo(a) system in an autochthonous Black African population from the Gabon.
European journal of human genetics : EJHG 2006;14(2):190-201.
2006: Judith Loeffler-Ragg; Martina Witsch-Baumgartner; Alexandar Tzankov; Wolfgang Hilbe; Ilona Schwentner; Georg M Sprinzl; Gerd Utermann; Heinz Zwierzina
Low incidence of mutations in EGFR kinase domain in Caucasian patients with head and neck squamous cell carcinoma.
European journal of cancer (Oxford, England : 1990) 2006;42(1):109-11.
2005: Debra A Thompson; Andreas R Janecke; Jessica Lange; Kecia L Feathers; Christian A Hübner; Christina L McHenry; David Wayne Stockton; Gabriele Rammesmayer; James R Lupski; Guillermo Antinolo; Carmen Ayuso; Montserrat Baiget; Peter Gouras; John R Heckenlively; Anneke I den Hollander; Samuel G Jacobson; Richard A Lewis; Paul Sieving; Bernd Wissinger; Suzanne Yzer; Eberhart Zrenner; Gerd Utermann; Andreas Gal
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle.
Human molecular genetics 2005;14(24):3865-75.
2005: Dieter Kotzot; Gerd Utermann
Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.
American journal of medical genetics. Part A 2005;136(3):287-305.
2005: Dieter Kotzot; Edda Haberlandt; Christine Fauth; Sara Baumgartner; Sabine Scholl-Bürgi; Gerd Utermann
Del(18)(q12.2q21.1) caused by a paternal sister chromatid rearrangement in a developmentally delayed girl.
American journal of medical genetics. Part A 2005;135(3):304-7.
2005: Martina Witsch-Baumgartner; P Clayton; N Clusellas; D Haas; Richard I Kelley; Malgorzata Krajewska-Walasek; S Lechner; M Rossi; J Zschocke; Gerd Utermann
Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy.
Human mutation 2005;25(4):412.
2005: Andreas R Janecke; Hans Christian Hennies; Barbara Günther; Gabriele Gansl; Josef Smolle; Elisabeth M Messmer; Gerd Utermann; Olaf Rittinger
GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal form.
American journal of medical genetics. Part A 2005;133A(2):128-31.
2005: Gabriel Miltenberger-Miltenyi; L Szonyi; L Balogh; Gerd Utermann; Andreas R Janecke
Mutation spectrum of type I glycogen storage disease in Hungary.
Journal of inherited metabolic disease 2005;28(6):939-44.
2004: Walther Parson; Hans Georg Kraft; Harald Niederstätter; Arno Lingenhel; Silvano Köchl; Friedrich Fresser; Gerd Utermann
A common nonsense mutation in the repetitive Kringle IV-2 domain of human apolipoprotein(a) results in a truncated protein and low plasma Lp(a).
Human mutation 2004;24(6):474-80.
2004: Elzbieta Ciara; Malgorzata J M Nowaczyk; Martina Witsch-Baumgartner; Ewa M Malunowicz; Ewa Popowska; Aleksandra Jezela-Stanek; M Piotrowicz; John S Waye; Gerd Utermann; Malgorzata Krajewska-Walasek
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndrome.
Clinical genetics 2004;66(6):517-24.
2004: Martina Witsch-Baumgartner; M Gruber; Hans Georg Kraft; M Rossi; P Clayton; M Giros; D Haas; Richard I Kelley; Malgorzata Krajewska-Walasek; Gerd Utermann
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome.
Journal of medical genetics 2004;41(8):577-84.
2004: Andreas R Janecke; Debra A Thompson; Gerd Utermann; Christian Becker; Christian A Hübner; Eduard Schmid; Christina L McHenry; Anita R Nair; Franz Rüschendorf; John R Heckenlively; Bernd Wissinger; Peter Nürnberg; Andreas Gal
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy.
Nature genetics 2004;36(8):850-4.
2004: Andreas R Janecke; Thomas Müller; Ingmar Gassner; Alfons Kreczy; Eduard Schmid; Florian Kronenberg; Barbara Utermann; Gerd Utermann
Joubert-like syndrome unlinked to known candidate loci.
The Journal of pediatrics 2004;144(2):264-9.
2003: Florian Kronenberg; Karl Lhotta; Paul König; Raimund Margreiter; Hans Dieplinger; Gerd Utermann
Apolipoprotein(a) isoform-specific changes of lipoprotein(a) after kidney transplantation.
European journal of human genetics : EJHG 2003;11(9):693-9.
2003: Barbara Günther; Andrea Steiner; Doris Nekahm-Heis; Klaus Albegger; Patrick Zorowka; Gerd Utermann; Andreas R Janecke
The 342-kb deletion in GJB6 is not present in patients with non-syndromic hearing loss from Austria.
Human mutation 2003;22(2):180.
2003: F S Geethanjali; Kalpana Luthra; Arno Lingenhel; A S Kanagasaba-Pathy; Jose Jacob; Lalit M Srivastava; Suman Vasisht; Hans Georg Kraft; Gerd Utermann
Analysis of the apo(a) size polymorphism in Asian Indian populations: association with Lp(a) concentration and coronary heart disease.
Atherosclerosis 2003;169(1):121-30.
2003: Judith Loeffler; Elisabeth Soelder; Martin Erdel; Barbara Utermann; Andreas R Janecke; Hans-Christoph Duba; Gerd Utermann
Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism.
American journal of medical genetics. Part A 2003;116A(3):290-4.
2002: Christina Lutz; Johannes Nimpf; Marcel Jenny; Karl Boecklinger; Christiane Enzinger; Gerd Utermann; Gabriele Baier-Bitterlich; Gottfried Baier
Evidence of functional modulation of the MEKK/JNK/cJun signaling cascade by the low density lipoprotein receptor-related protein (LRP).
The Journal of biological chemistry 2002;277(45):43143-51.
2002: Judith Loeffler; Gerd Utermann; Martina Witsch-Baumgartner
Molecular prenatal diagnosis of Smith-Lemli-Opitz syndrome is reliable and efficient.
Prenatal diagnosis 2002;22(9):827-30.
2002: Andreas R Janecke; Almut Hirst-Stadlmann; Barbara Günther; Barbara Utermann; Thomas Müller; Jürgen Löffler; Gerd Utermann; Doris Nekahm-Heis
Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria.
Human genetics 2002;111(2):145-53.
2002: Marjan M Nezarati; Judith Loeffler; Grace Yoon; Linda MacLaren; Ernest Fung; Floyd F Snyder; Gerd Utermann; Gail E Graham
Novel mutation in the Delta-sterol reductase gene in three Lebanese sibs with Smith-Lemli-Opitz (RSH) syndrome.
American journal of medical genetics 2002;110(2):103-8.
2002: A Kapetanopoulos; Friedrich Fresser; Gunda Millonig; Y Shaul; Gottfried Baier; Gerd Utermann
Direct interaction of the extracellular matrix protein DANCE with apolipoprotein(a) mediated by the kringle IV-type 2 domain.
Molecular genetics and genomics : MGG 2002;267(4):440-6.
2002: Hans-Christoph Duba; Andreas Doll; Michael Neyer; Martin Erdel; Christian Mann; Ignaz Hammerer; Gerd Utermann; Karl-Heinz Grzeschik
The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.
European journal of human genetics : EJHG 2002;10(6):351-61.
2002: Kurt Kofler; Martin Erdel; Gerd Utermann; Gottfried Baier
Molecular genetics and structural genomics of the human protein kinase C gene module.
Genome biology 2002;3(3):RESEARCH0014.
2001: Irmgard Verdorfer; Alfred Hobisch; Zoran Culig; Anton Hittmair; G Bartsch; Martin Erdel; Hans-Christoph Duba; Gerd Utermann
Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridization.
International journal of oncology 2001;19(6):1263-70.
2001: Martina Witsch-Baumgartner; J Loeffler; HJ Menzel; Gerd Utermann; C Neuhaus
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder.
American journal of medical genetics 2001;102(1):106-7.
2001: S Hass; Andreas Weidemann; Gerd Utermann; Gottfried Baier
Intracellular apolipoprotein E affects Amyloid Precursor Protein processing and amyloid Abeta production in COS-1 cells.
Molecular genetics and genomics : MGG 2001;265(5):791-800.
2001: Edda Haberlandt; Jürgen Löffler; Almut Hirst-Stadlmann; B Stöckl; W Judmaier; H Fischer; P Heinz-Erian; T Müller; Gerd Utermann; R J Smith; Andreas R Janecke
Split hand/split foot malformation associated with sensorineural deafness, inner and middle ear malformation, hypodontia, congenital vertical talus, and deletion of eight microsatellite markers in 7q21.1-q21.3.
Journal of medical genetics 2001;38(6):405-9.
2001: Andreas R Janecke; E Mayatepek; Gerd Utermann
Molecular genetics of type 1 glycogen storage disease.
Molecular genetics and metabolism 2001;73(2):117-25.
2001: M Ogorelkova; Hans Georg Kraft; C Ehnholm; Gerd Utermann
Single nucleotide polymorphisms in exons of the apo(a) kringles IV types 6 to 10 domain affect Lp(a) plasma concentrations and have different patterns in Africans and Caucasians.
Human molecular genetics 2001;10(8):815-24.
2001: Andreas R Janecke; D Nekahm; Jürgen Löffler; Almut Hirst-Stadlmann; Thomas Müller; Gerd Utermann
De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.
Human genetics 2001;108(3):269-70.
2001: Jürgen Löffler; D Nekahm; Almut Hirst-Stadlmann; Barbara Günther; HJ Menzel; Gerd Utermann; Andreas R Janecke
Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
European journal of human genetics : EJHG 2001;9(3):226-30.
2001: Martina Witsch-Baumgartner; Jürgen Löffler; Gerd Utermann
Mutations in the human DHCR7 gene.
Human mutation 2001;17(3):172-82.
2001: Martina Witsch-Baumgartner; Elzbieta Ciara; Jürgen Löffler; HJ Menzel; U Seedorf; J Burn; Gabriele Gillessen-Kaesbach; G F Hoffmann; Barbara U Fitzky; H Mundy; P Clayton; Richard I Kelley; Malgorzata Krajewska-Walasek; Gerd Utermann
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations.
European journal of human genetics : EJHG 2001;9(1):45-50.
2000: R Klose; Friedrich Fresser; S Kochl; Walther Parson; A Kapetanopoulos; J Fruchart-Najib; Gottfried Baier; Gerd Utermann
Mapping of a minimal apolipoprotein(a) interaction motif conserved in fibrin(ogen) beta - and gamma -chains.
The Journal of biological chemistry 2000;275(49):38206-12.
2000: Birgit Bauer; Nina Krumböck; Nassim Ghaffari Tabrizi; Sonja Kampfer; Andreas Villunger; Monika Wilda; H Hameister; Gerd Utermann; Michael Leitges; Florian Uberall; Gottfried Baier
T cell expressed PKCtheta demonstrates cell-type selective function.
European journal of immunology 2000;30(12):3645-54.
2000: Hans-Christoph Duba; Wolfgang Hilbe; A Mehringer; Martin Erdel; Josef Thaler; Gerd Utermann
Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemia.
International journal of oncology 2000;17(6):1245-9.
2000: Jürgen Löffler; A Trojovsky; B Casati; P M Kroisel; Gerd Utermann
Homozygosity for the W151X stop mutation in the delta7-sterol reductase gene (DHCR7) causing a lethal form of Smith-Lemli-Opitz syndrome: retrospective molecular diagnosis.
American journal of medical genetics 2000;95(2):174-7.
2000: Andreas R Janecke; M Lindner; Martin Erdel; E Mayatepek; Dorothea Möslinger; T Podskarbi; Friedrich Fresser; Sylvia Stöckler-Ipsiroglu; G F Hoffmann; Gerd Utermann
Mutation analysis in glycogen storage disease type 1 non-a.
Human genetics 2000;107(3):285-9.
2000: Jürgen Löffler; Barbara Utermann; Hans-Christoph Duba; U Mayr; Gerd Utermann; Martin Erdel
Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7).
American journal of medical genetics 2000;91(4):291-7.
2000: Charlotte L Scholtz; Arno Lingenhel; Renate Hillermann; I A Stander; J A Kriek; MP Marais; Hein J Odendaal; Hans Georg Kraft; Gerd Utermann; Maritha J Kotze
Lipoprotein(a) determination and risk of cardiovascular disease in South African patients with familial hypercholesterolaemia.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2000;90(4):374-8.
2000: Martina Witsch-Baumgartner; Barbara U Fitzky; M Ogorelkova; Hans Georg Kraft; Fabian F Moebius; Hartmut Glossmann; U Seedorf; Gabriele Gillessen-Kaesbach; G F Hoffmann; P Clayton; Richard I Kelley; Gerd Utermann
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome.
American journal of human genetics 2000;66(2):402-12.
2000: Hans Georg Kraft; Arno Lingenhel; Frederick J Raal; M Hohenegger; Gerd Utermann
Lipoprotein(a) in homozygous familial hypercholesterolemia.
Arteriosclerosis, thrombosis, and vascular biology 2000;20(2):522-8.
1999: M Ogorelkova; A Gruber; Gerd Utermann
Molecular basis of congenital lp(a) deficiency: a frequent apo(a) 'null' mutation in caucasians.
Human molecular genetics 1999;8(11):2087-96.
1999: Florian Kronenberg; Martina F Kronenberg; Stefan Kiechl; Evi Trenkwalder; Peter Santer; Friedrich Oberhollenzer; Georg Egger; Gerd Utermann; Johann Willeit
Role of lipoprotein(a) and apolipoprotein(a) phenotype in atherogenesis: prospective results from the Bruneck study.
Circulation 1999;100(11):1154-60.
1999: Florian Kronenberg; Martin Auinger; Evi Trenkwalder; Karl Irsigler; Gerd Utermann; Hans Dieplinger
Is apolipoprotein(a) a susceptibility gene for type I diabetes mellitus and related to long-term survival?
Diabetologia 1999;42(8):1021-7.
1999: Hans Dieplinger; Gerd Utermann
The seventh myth of lipoprotein(a): where and how is it assembled?
Current opinion in lipidology 1999;10(3):275-83.
1999: L Kerschdorfer; Paul König; Ulrich Neyer; Claudia Bösmüller; Karl Lhotta; Martin Auinger; M Hohenegger; Peter Riegler; Raimund Margreiter; Gerd Utermann; Hans Dieplinger; Florian Kronenberg
Lipoprotein(a) plasma concentrations after renal transplantation: a prospective evaluation after 4 years of follow-up.
Atherosclerosis 1999;144(2):381-91.
1999: Irmgard Verdorfer; Alfred Hobisch; Anton Hittmair; Hans-Christoph Duba; G Bartsch; Gerd Utermann; Martin Erdel
Cytogenetic characterization of 22 human renal cell tumors in relation to a histopathological classification.
Cancer genetics and cytogenetics 1999;111(1):61-70.
1999: Gerd Utermann
Genetic architecture and evolution of the lipoprotein(a) trait.
Current opinion in lipidology 1999;10(2):133-41.
1999: Barbara U Fitzky; Hartmut Glossmann; Gerd Utermann; Fabian F Moebius
Molecular genetics of the Smith-Lemli-Opitz syndrome and postsqualene sterol metabolism.
Current opinion in lipidology 1999;10(2):123-31.
1999: M F Kronenberg; HJ Menzel; Georg Ebersbach; Gregor Wenning; Elisabeth Luginger; M Gollner; Gerhard Ransmayr; Gerd Utermann; Werner Poewe; Florian Kronenberg
Dopamine D4 receptor polymorphism and idiopathic Parkinson's disease.
European journal of human genetics : EJHG 1999;7(3):397-400.
1999: Martin Erdel; Michael Hubalek; Arno Lingenhel; Kurt Kofler; Hans-Christoph Duba; Gerd Utermann
Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH.
Nature genetics 1999;21(4):357-8.
1999: M Scholz; Hans Georg Kraft; Arno Lingenhel; Rhena Delport; E H Vorster; H Bickeböller; Gerd Utermann
Genetic control of lipoprotein(a) concentrations is different in Africans and Caucasians.
European journal of human genetics : EJHG 1999;7(2):169-78.
1999: Asli N Silahtaroglu; Frans A Hol; Peter Koch Jensen; Martin Erdel; Hans-Christoph Duba; MP Geurds; Nine V A M Knoers; Edwin C M Mariman; Zeynep Tümer; Gerd Utermann; Jutta Wirth; Merete Bugge; Niels Tommerup
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome.
European journal of human genetics : EJHG 1999;7(1):68-76.
1999: Nassim Ghaffari Tabrizi; Birgit Bauer; Andreas Villunger; Gabriele Baier-Bitterlich; A Altman; Gerd Utermann; Florian Uberall; Gottfried Baier
Protein kinase Ctheta, a selective upstream regulator of JNK/SAPK and IL-2 promoter activation in Jurkat T cells.
European journal of immunology 1999;29(1):132-42.
1999: Hans-Christoph Duba; S Peter; Wolfgang Hilbe; T Fluckinger; Michael Fridrik; Martin Erdel; Josef Thaler; Gerd Utermann
Monitoring of remission status by fluorescence in situ hybridisation in chronic myeloid leukaemia patients treated with interferon-alpha.
International journal of oncology 1999;14(1):145-50.
1998: Florian Kronenberg; Evi Trenkwalder; Martina F Kronenberg; Paul König; Gerd Utermann; Hans Dieplinger
Influence of hematocrit on the measurement of lipoproteins demonstrated by the example of lipoprotein(a).
Kidney international 1998;54(4):1385-9.
1998: Kurt Kofler; Silvano Köchl; Walther Parson; Martin Erdel; Gerd Utermann; Gottfried Baier
Molecular characterization of the human protein kinase C theta gene locus (PRKCQ).
Molecular & general genetics : MGG 1998;259(4):398-403.
1998: Siegfried Waldegger; Martin Erdel; UO Nagl; P Barth; G Raber; S Steuer; Gerd Utermann; Markus Paulmichl; Florian Lang
Genomic organization and chromosomal localization of the human SGK protein kinase gene.
Genomics 1998;51(2):299-302.
1998: Barbara U Fitzky; Martina Witsch-Baumgartner; M Erdel; Joon No Lee; Young-Ki Paik; Hartmut Glossmann; Gerd Utermann; Fabian F Moebius
Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(14):8181-6.
1998: S Hass; Friedrich Fresser; Silvano Köchl; Konrad Beyreuther; Gerd Utermann; Gottfried Baier
Physical interaction of ApoE with amyloid precursor protein independent of the amyloid Abeta region in vitro.
The Journal of biological chemistry 1998;273(22):13892-7.
1998: Eva M Lobentanz; K Krasznai; A Gruber; C Brunner; H J Müller; J Sattler; Hans Georg Kraft; Gerd Utermann; Hans Dieplinger
Intracellular metabolism of human apolipoprotein(a) in stably transfected Hep G2 cells.
Biochemistry 1998;37(16):5417-25.
1998: UO Nagl; Martin Erdel; F Bergmann; Bernhard Oehl; Elke Scandella; Luca Musante; Luis J V Galietta; Martin Gschwentner; Johannes Fürst; A Schmarda; S Hofer; Gerd Utermann; Peter Deetjen; Markus Paulmichl
Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localization.
Gene 1998;209(1-2):59-63.
1998: C Haibach; Hans Georg Kraft; Silvano Köchl; A Abe; Gerd Utermann
The number of kringle IV repeats 3-10 is invariable in the human apo(a) gene.
Gene 1998;208(2):253-8.
1998: J Mühlmann; Josef Thaler; Wolfgang Hilbe; Oliver E Bechter; Martin Erdel; Gerd Utermann; Hans-Christoph Duba
Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: a new strategy for remission assessment.
Genes, chromosomes & cancer 1998;21(2):90-100.
1998: Hans Georg Kraft; M Windegger; HJ Menzel; Gerd Utermann
Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibrium.
Human molecular genetics 1998;7(2):257-64.
1998: Hans-Christoph Duba; Martin Erdel; Jürgen Löffler; Jutta Wirth; Barbara Utermann; Gerd Utermann
Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier.
European journal of human genetics : EJHG 1998;6(1):75-9.
1998: Arno Lingenhel; Hans Georg Kraft; Maritha J Kotze; A V Peeters; Florian Kronenberg; R Kruse; Gerd Utermann
Concentrations of the atherogenic Lp(a) are elevated in FH.
European journal of human genetics : EJHG 1998;6(1):50-60.
1997: Florian Kronenberg; Evi Trenkwalder; Wolfgang Sturm; Hermann Kathrein; Paul König; Ulrich Neyer; E Gröchenig; Gerd Utermann; Hans Dieplinger
LDL-unbound apolipoprotein(a) and carotid atherosclerosis in hemodialysis patients.
Clinical genetics 1997;52(5):377-86.
1997: Florian Kronenberg; Evi Trenkwalder; Arno Lingenhel; Guy Friedrich; Karl Lhotta; M Schober; Nicolas Moes; Paul König; Gerd Utermann; Hans Dieplinger
Renovascular arteriovenous differences in Lp[a] plasma concentrations suggest removal of Lp[a] from the renal circulation.
Journal of lipid research 1997;38(9):1755-63.
1997: Hans-Christoph Duba; Harald Weirich; Helga Weirich-Schwaiger; Barbara Utermann; David Nachbaur; E Sölder; Gerd Utermann
Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome?
Human genetics 1997;100(3-4):431-40.
1997: Ralf Weiskirchen; Martin Erdel; Gerd Utermann; Klaus Bister
Cloning, structural analysis, and chromosomal localization of the human CSRP2 gene encoding the LIM domain protein CRP2.
Genomics 1997;44(1):83-93.
1997: Silvano Köchl; Friedrich Fresser; Eva M Lobentanz; Gottfried Baier; Gerd Utermann
Novel interaction of apolipoprotein(a) with beta-2 glycoprotein I mediated by the kringle IV domain.
Blood 1997;90(4):1482-9.
1997: Y Y van der Hoek; Arno Lingenhel; Hans Georg Kraft; Joep C Defesche; John J P Kastelein; Gerd Utermann
Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.
The Journal of clinical investigation 1997;99(9):2269-73.
1997: Martin Erdel; Hans-Christoph Duba; Irmgard Verdorfer; Arno Lingenhel; R Geiger; K H Gutenberger; E Ludescher; Barbara Utermann; Gerd Utermann
Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.
Human genetics 1997;99(5):596-601.
1997: Hans-Christoph Duba; Martin Erdel; Jürgen Löffler; L Bereuther; H Fischer; Barbara Utermann; Gerd Utermann
Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
Journal of medical genetics 1997;34(4):309-13.
1997: Gerd Utermann
Genetic services in Austria.
European journal of human genetics : EJHG 1997;5 Suppl 2():31-4.
1996: UO Nagl; Martin Erdel; A Schmarda; Marco Seri; Germar-M. Pinggera; Martin Gschwentner; C Duba; Luis J V Galietta; Peter Deetjen; Gerd Utermann; Markus Paulmichl
Chromosomal localization of the genes (CLNS1A and CLNS1B) coding for the swelling-dependent chloride channel ICln.
Genomics 1996;38(3):438-41.
1996: C Brunner; Eva M Lobentanz; A Pethö-Schramm; A Ernst; C Kang; Hans Dieplinger; H J Müller; Gerd Utermann
The number of identical kringle IV repeats in apolipoprotein(a) affects its processing and secretion by HepG2 cells.
The Journal of biological chemistry 1996;271(50):32403-10.
1996: Florian Kronenberg; Evi Trenkwalder; Hans Dieplinger; Gerd Utermann
Lipoprotein(a) in stored plasma samples and the ravages of time. Why epidemiological studies might fail.
Arteriosclerosis, thrombosis, and vascular biology 1996;16(12):1568-72.
1996: Hans Georg Kraft; Arno Lingenhel; giovanni bader; Gerhard Kostner; Gerd Utermann
The relative electrophoretic mobility of apo(a) isoforms depends on the gel system: proposal of a nomenclature for apo(a) phenotypes.
Atherosclerosis 1996;125(1):53-61.
1996: Bernhard Föger; Alfred Königsrainer; G Palos; Andreas Ritsch; G Tröbinger; H J Menzel; Monika Lechleitner; A Doblinger; P König; Gerd Utermann; Raimund Margreiter; Josef R Patsch
Effects of pancreas transplantation on distribution and composition of plasma lipoproteins.
Metabolism: clinical and experimental 1996;45(7):856-61.
1996: Josef Thaler; Guenther Gastl; T Fluckinger; Dietger Niederwieser; Heinz Huber; HL Seewann; Heinz Sill; A Lang; M Falk; C Duba; Gerd Utermann; Thomas Kühr; Walter Aulitzky; Christoph Huber
Interferon alpha-2c therapy of patients with chronic myelogenous leukemia: long-term results of a multicenter phase-II study. Austrian Biological Response Modifier (BRM) Study Group.
Annals of hematology 1996;72(6):349-55.
1996: Florian Kronenberg; Hans Dieplinger; Paul König; Gerd Utermann
Lipoprotein metabolism in renal replacement therapy: a review.
Israel journal of medical sciences 1996;32(6):371-89.
1996: Martin Erdel; S Schuffenhauer; B Buchholz; U Barth-Witte; Silvano Köchl; Barbara Utermann; Hans-Christoph Duba; Gerd Utermann
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
Human genetics 1996;97(6):784-93.
1996: Hans Georg Kraft; Arno Lingenhel; Silvano Köchl; Friedrich Hoppichler; Florian Kronenberg; A Abe; V Mühlberger; Diether Schönitzer; Gerd Utermann
Apolipoprotein(a) kringle IV repeat number predicts risk for coronary heart disease.
Arteriosclerosis, thrombosis, and vascular biology 1996;16(6):713-9.
1996: Friedrich Hoppichler; Hans Georg Kraft; C Sandholzer; Monika Lechleitner; Josef R Patsch; Gerd Utermann
Lipoprotein(a) is increased in triglyceride-rich lipoproteins in men with coronary heart disease, but does not change acutely following oral fat ingestion.
Atherosclerosis 1996;122(1):127-34.
1996: Gabriele Baier-Bitterlich; Florian Uberall; Birgit Bauer; Friedrich Fresser; H Wachter; Hans H Grunicke; Gerd Utermann; A Altman; Gottfried Baier
Protein kinase C-theta isoenzyme selective stimulation of the transcription factor complex AP-1 in T lymphocytes.
Molecular and cellular biology 1996;16(4):1842-50.
1996: Hans Georg Kraft; Arno Lingenhel; Richard Pang; Rhena Delport; M Trommsdorff; H Vermaak; Edward D Janus; Gerd Utermann
Frequency distributions of apolipoprotein(a) kringle IV repeat alleles and their effects on lipoprotein(a) levels in Caucasian, Asian, and African populations: the distribution of null alleles is non-random.
European journal of human genetics : EJHG 1996;4(2):74-87.
1996: Florian Kronenberg; Gerd Utermann; Hans Dieplinger
Lipoprotein(a) in renal disease.
American journal of kidney diseases : the official journal of the National Kidney Foundation 1996;27(1):1-25.
1995: Bernhard Föger; G Tröbinger; Andreas Ritsch; Monika Lechleitner; T Hopferwieser; H J Menzel; Gerd Utermann; K P Pfeiffer; Josef R Patsch
Treatment of primary mixed hyperlipidemia with etophylline clofibrate: effects on lipoprotein-modifying enzymes, postprandial lipoprotein metabolism, and lipoprotein distribution and composition.
Atherosclerosis 1995;117(2):253-61.
1995: S Bopp; Silvano Köchl; Francesco Acquati; P Magnaghi; A Pethö-Schramm; Hans Georg Kraft; Gerd Utermann; H J Müller; Roberto Taramelli
Ten allelic apolipoprotein[a] 5' flanking fragments exhibit comparable promoter activities in HepG2 cells.
Journal of lipid research 1995;36(8):1721-8.
1995: M Trommsdorff; Silvano Köchl; Arno Lingenhel; Florian Kronenberg; Rhena Delport; H Vermaak; L Lemming; Ib C Klausen; Ole Faergeman; Gerd Utermann
A pentanucleotide repeat polymorphism in the 5' control region of the apolipoprotein(a) gene is associated with lipoprotein(a) plasma concentrations in Caucasians.
The Journal of clinical investigation 1995;96(1):150-7.
1995: Florian Kronenberg; Paul König; Ulrich Neyer; Martin Auinger; A Pribasnig; U Lang; J Reitinger; G Pinter; Gerd Utermann; Hans Dieplinger
Multicenter study of lipoprotein(a) and apolipoprotein(a) phenotypes in patients with end-stage renal disease treated by hemodialysis or continuous ambulatory peritoneal dialysis.
Journal of the American Society of Nephrology : JASN 1995;6(1):110-20.
1995: Friedrich Hoppichler; C Sandholzer; Roy Moncayo; Gerd Utermann; Hans Georg Kraft
Thyroid hormone (fT4) reduces lipoprotein(a) plasma levels.
Atherosclerosis 1995;115(1):65-71.
1995: A Orou; B Fechner; H J Menzel; Gerd Utermann
Automatic separation of two PCRs in one tube by annealing temperature.
Trends in genetics : TIG 1995;11(4):127-8.
1995: Hans Georg Kraft; C Haibach; Arno Lingenhel; C Brunner; M Trommsdorff; Florian Kronenberg; H J Müller; Gerd Utermann
Sequence polymorphism in kringle IV 37 in linkage disequilibrium with the apolipoprotein (a) size polymorphism.
Human genetics 1995;95(3):275-82.
1995: Martin Erdel; Gabriele Baier-Bitterlich; C Duba; N Isakov; A Altman; Gerd Utermann; Gottfried Baier
Mapping of the human protein kinase C-theta (PRKCQ) gene locus to the short arm of chromosome 10 (10p15) by FISH.
Genomics 1995;25(2):595-7.
1995: Gerd Utermann; C Haibach; M Trommsdorff; Silvano Köchl; Arno Lingenhel; A Abe; Hans Georg Kraft
Genetic architecture of the atherogenic lipoprotein(a).
Annals of the New York Academy of Sciences 1995;748():301-11; discussion 311-2.
1995: C Sandholzer; Rhena Delport; H Vermaak; Gerd Utermann
High frequency of the apo epsilon 4 allele in Khoi San from South Africa.
Human genetics 1995;95(1):46-8.
1995: H J Menzel; Hans Dieplinger; C Sandholzer; István Karádi; Gerd Utermann; Albert Császár
Apolipoprotein A-IV polymorphism in the Hungarian population: gene frequencies, effect on lipid levels, and sequence of two new variants.
Human mutation 1995;5(1):58-65.
1995: A Orou; B Fechner; Gerd Utermann; H J Menzel
Allele-specific competitive blocker PCR: a one-step method with applicability to pool screening.
Human mutation 1995;6(2):163-9.
1994: Sasa Frank; K Krasznai; S Durovic; Eva M Lobentanz; Hans Dieplinger; Ernst Wagner; K Zatloukal; M Cotten; Gerd Utermann; Gerhard Kostner
High-level expression of various apolipoprotein(a) isoforms by "transferrinfection": the role of kringle IV sequences in the extracellular association with low-density lipoprotein.
Biochemistry 1994;33(40):12329-39.
1994: Florian Kronenberg; H Kathrein; Paul König; Ulrich Neyer; Wolfgang Sturm; Karl Lhotta; E Gröchenig; Gerd Utermann; Hans Dieplinger
Apolipoprotein(a) phenotypes predict the risk for carotid atherosclerosis in patients with end-stage renal disease.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1994;14(9):1405-11.
1994: Florian Kronenberg; Paul König; Karl Lhotta; D Ofner; C Sandholzer; Raimund Margreiter; E Dosch; Gerd Utermann; Hans Dieplinger
Apolipoprotein(a) phenotype-associated decrease in lipoprotein(a) plasma concentrations after renal transplantation.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1994;14(9):1399-404.
1994: Florian Kronenberg; Eva M Lobentanz; Paul König; Gerd Utermann; Hans Dieplinger
Effect of sample storage on the measurement of lipoprotein[a], apolipoproteins B and A-IV, total and high density lipoprotein cholesterol and triglycerides.
Journal of lipid research 1994;35(7):1318-28.
1994: Florian Kronenberg; Gerd Utermann
[Lipoprotein(a)--atherogenic waste product of evolution?].
Wiener medizinische Wochenschrift (1946) 1994;144(12-13):324-30.
1993: C Brunner; Hans Georg Kraft; Gerd Utermann; H J Müller
Cys4057 of apolipoprotein(a) is essential for lipoprotein(a) assembly.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(24):11643-7.
1993: Hans Georg Kraft; N Malgaretti; Silvano Köchl; Francesco Acquati; Gerd Utermann; Roberto Taramelli
Demonstration of physical linkage between the promoter region and the polymorphic kringle IV domain in the Apo(a) gene by pulsed-field gel electrophoresis.
Genomics 1993;17(1):260-2.
1993: Florian Kronenberg; Paul König; Karl Lhotta; A Königsrainer; C Sandholzer; Gerd Utermann; Hans Dieplinger
Cyclosporin and serum lipids in renal transplant recipients.
Lancet 1993;341(8847):765; author reply 767.
1993: Albert Császár; Hans Dieplinger; C Sandholzer; István Karádi; E Juhász; H Drexel; T Halmos; László Romics; Josef R Patsch; Gerd Utermann
Plasma lipoprotein (a) concentration and phenotypes in diabetes mellitus.
Diabetologia 1993;36(1):47-51.
1992: C Sandholzer; G Feussner; J Brunzell; Gerd Utermann
Distribution of apolipoprotein(a) in the plasma from patients with lipoprotein lipase deficiency and with type III hyperlipoproteinemia. No evidence for a triglyceride-rich precursor of lipoprotein(a).
The Journal of clinical investigation 1992;90(5):1958-65.
1992: Hans Georg Kraft; Silvano Köchl; H J Menzel; C Sandholzer; Gerd Utermann
The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration.
Human genetics 1992;90(3):220-30.
1992: C Sandholzer; N Saha; J D Kark; A Rees; W Jaross; Hans Dieplinger; Friedrich Hoppichler; Eric Boerwinkle; Gerd Utermann
Apo(a) isoforms predict risk for coronary heart disease. A study in six populations.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1992;12(10):1214-26.
1992: Hans Dieplinger; Eva M Lobentanz; Paul König; H Graf; C Sandholzer; E Matthys; M Rosseneu; Gerd Utermann
Plasma apolipoprotein A-IV metabolism in patients with chronic renal disease.
European journal of clinical investigation 1992;22(3):166-74.
1992: C Sandholzer; Eric Boerwinkle; N Saha; M C Tong; Gerd Utermann
Apolipoprotein(a) phenotypes, Lp(a) concentration and plasma lipid levels in relation to coronary heart disease in a Chinese population: evidence for the role of the apo(a) gene in coronary heart disease.
The Journal of clinical investigation 1992;89(3):1040-6.
1992: Hans Georg Kraft; C Sandholzer; H J Menzel; Gerd Utermann
Apolipoprotein (a) alleles determine lipoprotein (a) particle density and concentration in plasma.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1992;12(3):302-6.
1991: D M Hallman; Eric Boerwinkle; N Saha; C Sandholzer; H J Menzel; A Csázár; Gerd Utermann
The apolipoprotein E polymorphism: a comparison of allele frequencies and effects in nine populations.
American journal of human genetics 1991;49(2):338-49.
1991: C Sandholzer; D M Hallman; N Saha; G Sigurdsson; Carolin Lackner; Albert Császár; Eric Boerwinkle; Gerd Utermann
Effects of the apolipoprotein(a) size polymorphism on the lipoprotein(a) concentration in 7 ethnic groups.
Human genetics 1991;86(6):607-14.
1990: Albert Császár; László Romics; Carolin Lackner; Hans Dieplinger; István Karádi; Gerd Utermann
[Plasma concentration of lipoprotein(a) and distribution of its subtypes in the healthy population of Hungary].
Orvosi hetilap 1990;131(38):2071-5.
1990: Mary Seed; Friedrich Hoppichler; David A Reaveley; S McCarthy; G R Thompson; Eric Boerwinkle; Gerd Utermann
Relation of serum lipoprotein(a) concentration and apolipoprotein(a) phenotype to coronary heart disease in patients with familial hypercholesterolemia.
The New England journal of medicine 1990;322(21):1494-9.
1990: G Lindahl; E Gersdorf; H J Menzel; M Seed; S Humphries; Gerd Utermann
Variation in the size of human apolipoprotein(a) is due to a hypervariable region in the gene.
Human genetics 1990;84(6):563-7.
1990: H J Menzel; G Sigurdsson; Eric Boerwinkle; S Schrangl-Will; Hans Dieplinger; Gerd Utermann
Frequency and effect of human apolipoprotein A-IV polymorphism on lipid and lipoprotein levels in an Icelandic population.
Human genetics 1990;84(4):344-6.
1990: E Gersdorf; B Utermann; Gerd Utermann
Trisomy 18 mosaicism in an adult woman with normal intelligence and history of miscarriage.
Human genetics 1990;84(3):298-9.
1990: H J Menzel; Hans Dieplinger; Carolin Lackner; Friedrich Hoppichler; J K Lloyd; D R Muller; C Labeur; Philippa J Talmud; Gerd Utermann
Abetalipoproteinemia with an ApoB-100-lipoprotein(a) glycoprotein complex in plasma. Indication for an assembly defect.
The Journal of biological chemistry 1990;265(2):981-6.
1989: Gerd Utermann
The mysteries of lipoprotein(a).
Science (New York, N.Y.) 1989;246(4932):904-10.
1989: Gerd Utermann; Friedrich Hoppichler; Hans Dieplinger; Mary Seed; G Thompson; Eric Boerwinkle
Defects in the low density lipoprotein receptor gene affect lipoprotein (a) levels: multiplicative interaction of two gene loci associated with premature atherosclerosis.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(11):4171-4.
1989: Eric Boerwinkle; H J Menzel; Hans Georg Kraft; Gerd Utermann
Genetics of the quantitative Lp(a) lipoprotein trait. III. Contribution of Lp(a) glycoprotein phenotypes to normal lipid variation.
Human genetics 1989;82(1):73-8.
1989: G Lindahl; E Gersdorf; H J Menzel; C Duba; H Cleve; S Humphries; Gerd Utermann
The gene for the Lp(a)-specific glycoprotein is closely linked to the gene for plasminogen on chromosome 6.
Human genetics 1989;81(2):149-52.
1989: Hans Georg Kraft; H J Menzel; Friedrich Hoppichler; W Vogel; Gerd Utermann
Changes of genetic apolipoprotein phenotypes caused by liver transplantation. Implications for apolipoprotein synthesis.
The Journal of clinical investigation 1989;83(1):137-42.
1988: H J Menzel; Eric Boerwinkle; S Schrangl-Will; Gerd Utermann
Human apolipoprotein A-IV polymorphism: frequency and effect on lipid and lipoprotein levels.
Human genetics 1988;79(4):368-72.
1988: Hans Georg Kraft; Hans Dieplinger; E Hoye; Gerd Utermann
Lp(a) phenotyping by immunoblotting with polyclonal and monoclonal antibodies.
Arteriosclerosis (Dallas, Tex.) 1988;8(3):212-6.
1988: Eric Boerwinkle; Gerd Utermann
Simultaneous effects of the apolipoprotein E polymorphism on apolipoprotein E, apolipoprotein B, and cholesterol metabolism.
American journal of human genetics 1988;42(1):104-12.
1988: Gerd Utermann
Apolipoprotein polymorphism and multifactorial hyperlipidaemia.
Journal of inherited metabolic disease 1988;11 Suppl 1():74-86.
1988: H J Menzel; Gerd Utermann
The significance of apolipoprotein variants.
Progress in clinical and biological research 1988;255():63-72.
1988: Gerd Utermann; Hans Georg Kraft; H J Menzel; T Hopferwieser; C Seitz
Genetics of the quantitative Lp(a) lipoprotein trait. I. Relation of LP(a) glycoprotein phenotypes to Lp(a) lipoprotein concentrations in plasma.
Human genetics 1988;78(1):41-6.
1988: Gerd Utermann; C Duba; H J Menzel
Genetics of the quantitative Lp(a) lipoprotein trait. II. Inheritance of Lp(a) glycoprotein phenotypes.
Human genetics 1988;78(1):47-50.
1987: Gerd Utermann; H J Menzel; Hans Georg Kraft; H C Duba; H G Kemmler; C Seitz
Lp(a) glycoprotein phenotypes. Inheritance and relation to Lp(a)-lipoprotein concentrations in plasma.
The Journal of clinical investigation 1987;80(2):458-65.
1987: Gerd Utermann
Apolipoproteins, quantitative lipoprotein traits and multifactorial hyperlipidaemia.
Ciba Foundation symposium 1987;130():52-69.