H. Knoblauch

发表

Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications.

P. de Knijff, D. Labuda, O. Lao, 2010, American journal of human genetics.

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

H. Knoblauch, B. Horsthemke, W. Robinson, 1992, Human Genetics.

Support for linkage of familial combined hyperlipidemia to chromosome 1q21–q23 in Chinese and German families

Andreas Busjahn, Heike Baron, Herbert Schuster, 2000, Clinical genetics.

Heritability analysis of lipids and three gene loci in twins link the macrophage scavenger receptor to HDL cholesterol concentrations.

H. Knoblauch, A. Busjahn, F. Luft, 1997, Arteriosclerosis, thrombosis, and vascular biology.

A Xanthomatosis-Susceptibility Gene May Exist in a Syrian Family with Familial Hypercholesterolemia

H. Knoblauch, F. Luft, B. Mueller-Myhsok, 1997, European journal of human genetics : EJHG.

Chymase gene locus is not associated with myocardial infarction and is not linked to heart size or blood pressure.

T. Wienker, A. Pfeufer, H. Knoblauch, 1998, The American journal of cardiology.

A region on chromosome 3 is linked to dizygotic twinning

J. Kaprio, J. Tuomilehto, B. Müller-Myhsok, 2000, Nature Genetics.

Angiotensin-converting enzyme and angiotensinogen gene polymorphisms, plasma levels, cardiac dimensions. A twin study.

H. Knoblauch, A. Busjahn, F. Luft, 1997, Hypertension.

Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly.

T. Wienker, R. Fahlbusch, H. Knoblauch, 1997, Stroke.

Angiotensin-converting enzyme and angiotensinogen gene polymorphisms and heart rate variability in twins.

A Voss, N Wessel, R Dietz, 1998, The American journal of cardiology.

A new mutation in the elastin gene causing supravalvular aortic stenosis.

B. Müller-Myhsok, H. Knoblauch, F. Luft, 1999, The American journal of cardiology.

Increased Parental Ages and Uniparental Disomy 15: A Paternal Age Effect?

S. Schuffenhauer, H. Knoblauch, S. Langlois, 1993, European journal of human genetics : EJHG.

Expansion of the Phenotypic Spectrum of the CACNA1A T666M Mutation: A Family with Familial Hemiplegic Migraine Type 1, Cerebellar Atrophy and Mental Retardation

M. Dichgans, B. Müller-Myhsok, H. Knoblauch, 2008, Cephalalgia : an international journal of headache.

Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation

A. Spuler, H. Knoblauch, P. Nürnberg, 2010, Annals of neurology.

Clinical and molecular cytogenetic studies of a large de novo interstitial deletion 16q11.2-16q21 including the putative transcription factor geneSALL1

R. Chaoui, H. Knoblauch, S. Tinschert, 2000, Journal of medical genetics.

Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome

H. Knoblauch, G. Rappold, B. Schechinger, 2000, European Journal of Human Genetics.

Sudden death and Wegener's granulomatosis of the pituitary.

H. Knoblauch, R. Kettritz, A. Woywodt, 2000, Scandinavian journal of rheumatology.

Peroxisome proliferator-activated receptor gamma gene locus is related to body mass index and lipid values in healthy nonobese subjects.

B. Müller-Myhsok, H. Knoblauch, A. Busjahn, 1999, Arteriosclerosis, thrombosis, and vascular biology.

Insulin resistance in healthy prepubertal twins.

H. Knoblauch, F. Luft, P. Hofman, 2004, The Journal of pediatrics.

Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol.

J. Reich, H. Knoblauch, F. Luft, 2004, Human molecular genetics.

Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population.

Laurent Essioux, Herbert Schuster, Klaus Rohde, 2002, Human molecular genetics.

DNA Testing for Familial Hypercholesterolemia

Herbert Schuster, H. Knoblauch, Hans Knoblauch, 2002 .

A cholesterol-lowering gene maps to chromosome 13q.

S. Heath, B. Müller-Myhsok, Y. Friedlander, 2000, American journal of human genetics.

Fetal Trisomy 10 Mosaicism: Ultrasound, Cytogenetic and Morphologic Findings in Early Pregnancy

H. Knoblauch, S. Tinschert, C. Tennstedt, 1999, Prenatal diagnosis.

QT interval is linked to 2 long-QT syndrome loci in normal subjects.

H. Knoblauch, A. Busjahn, F. Luft, 1999, Circulation.

Concordant Association of Lipid Gene Variation with a Combined HDL/LDL-Cholesterol Phenotype in Two European Populations

J. Reich, M. Costanza, H. Knoblauch, 2006, Human Heredity.

Two brothers with findings resembling congenital intrauterine infection‐like syndrome (pseudo‐TORCH syndrome)

F. Hanefeld, T. Vulliamy, H. Knoblauch, 2003, American journal of medical genetics. Part A.

SALL 1 including the putative transcription factor gene 16 q 11 . 2-16 q 21 large de novo interstitial deletion Clinical and molecular cytogenetic studies of a

R. Chaoui, H. Knoblauch, S. Tinschert, 2022 .

A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum

A. Lumsden, K. Lindpaintner, H. Knoblauch, 2001, Journal of Molecular Medicine.

Tipslllilll A Nonisotopic Single-strand Conformation Polymorphism Protocol Using a Direct Blotting Electrophoresis , a Chemiluminescent Detection S stem , and a Multiplex Approach

Christiane, Keller, H. Knoblauch, 2007 .

Quantitative trait loci for blood pressure exist near the IGF-1, the Liddle syndrome, the angiotensin II-receptor gene and the renin loci in man.

B. Müller-Myhsok, H. Knoblauch, A. Busjahn, 1999, Journal of the American Society of Nephrology : JASN.

Single Nucleotide Polymorphism Haplotypes in the Cholesteryl-Ester Transfer Protein (CETP) Gene and Lipid Phenotypes

J. Reich, H. Knoblauch, F. Luft, 2003, Human Heredity.

Another side to statin-related side effects.

H. Knoblauch, W. Kress, S. Spuler, 2010, Annals of internal medicine.

A pathway model of lipid metabolism to predict the effect of genetic variability on lipid levels

Friedrich C. Luft, Herbert Schuster, J. Reich, 2000, Journal of Molecular Medicine.

Improving global and regional resolution of male lineage differentiation by simple single-copy Y-chromosomal short tandem repeat polymorphisms.

C. Tyler-Smith, Yali Xue, P. de Knijff, 2009, Forensic science international. Genetics.

Monozygotic Twins Concordant for Female-to-Male Transsexualism: A Case Report

H. Knoblauch, A. Busjahn, B. Wegener, 2007, Archives of sexual behavior.

Linkage but lack of association for blood pressure and the α-adducin locus in normotensive twins

H. Knoblauch, A. Busjahn, F. Luft, 1999 .

Linkage but lack of association for blood pressure and the alpha-adducin locus in normotensive twins.

H. Knoblauch, A. Busjahn, F. Luft, 1999, Journal of Hypertension.

DNA testing for familial hypercholesterolemia: improving disease recognition and patient care.

Herbert Schuster, H. Knoblauch, Hans Knoblauch, 2002, American journal of pharmacogenomics : genomics-related research in drug development and clinical practice.