Interaction of αPIX (ARHGEF6) with β-parvin (PARVB) suggests an involvement of αPIX in integrin-mediated signalingROSENBERGER, Georg; JANTKE, Inka; GAL, Andreas et al.Human molecular genetics (Print). 2003, Vol 12, Num 2, pp 155-167, issn 0964-6906, 13 p.Article

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3KORNAK, Uwe; MADEMAN, Inès; POU-SERRADELL, Adolf et al.Brain. 2014, Vol 137, pp 683-692, issn 0006-8950, 10 p., 3Article

Female carriers of X-chromosomal adrenoleukodystrophy: a major differential diagnosis in progressive myelopathyGUETTSCHES, Anne-Katrin; KUECHLER, Alma; GAL, Andreas et al.Journal of neurology. 2010, Vol 257, Num 8, pp 1394-1395, issn 0340-5354, 2 p.Article

Mucopolysaccharidosis type II in females : Case report and review of literatureTUSCHL, Karin; GAL, Andreas; PASCHKE, Eduard et al.Pediatric neurology. 2005, Vol 32, Num 4, pp 270-272, issn 0887-8994, 3 p.Article

Familiäre Foveahypoplasie: Klinische Einordnung = Hereditary foveal hypoplasia: Clinical differentiationSCHROEDER, Hans Wolfgang; ORTH, Ulrike; MEYER-KÖNIG, Eberhard et al.Klinische Monatsblätter für Augenheilkunde. 2003, Vol 220, Num 8, pp 559-562, issn 0023-2165, 4 p.Article

The early clinical phenotype of Fabry disease: a study on 35 European children and adolescentsRIES, Markus; RAMASWAMI, Uma; PARINI, Rossella et al.European journal of pediatrics. 2003, Vol 162, Num 11, pp 767-772, issn 0340-6199, 6 p.Article

No association between DCP1 genotype and late-onset Alzheimer diseaseBUSS, Svenja; MÜLLER-THOMSEN, Tomas; HOCK, Cristoph et al.American journal of medical genetics. 2002, Vol 114, Num 4, pp 440-445, issn 0148-7299Article

Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationKUTSCHE, Kerstin; YNTEMA, Helger; MORAINE, Claude et al.Nature genetics. 2000, Vol 26, Num 2, pp 247-250, issn 1061-4036Article

Compartmental Memory Management in a Modern Web BrowserWAGNER, Gregor; GAL, Andreas; WIMMER, Christian et al.ACM SIGPLAN notices. 2011, Vol 46, Num 11, pp 119-128, issn 1523-2867, 10 p.Article

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesDUFKE, Claudia; SCHLIPF, Nina; KLOPSTOCK, Thomas et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 215-227, issn 1364-6745, 13 p.Article

Onset and progression of the Anderson-Fabry disease related cardiomyopathyKAMPMANN, Christoph; LINHART, Ales; BAEHNER, Frank et al.International journal of cardiology. 2008, Vol 130, Num 3, pp 367-373, issn 0167-5273, 7 p.Article

The phenotype of early-onset retinal degeneration in persons with RDH12 mutationsSCHUSTER, Andreas; JANECKE, Andreas R; WILKE, Robert et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 4, pp 1824-1831, issn 0146-0404, 8 p.Article

Differences in methylation patterns in the methylation boundary region of IDS gene in hunter syndrome patients: implications for CpG hot spot mutationsTOMATSU, Shunji; SUKEGAWA, Kazuko; COOPER, Alan et al.European journal of human genetics. 2006, Vol 14, Num 7, pp 838-845, issn 1018-4813, 8 p.Article

Advanced renal insufficiency in a 34-year-old man with Lowe syndromeSCHRAMM, Lothar; GAL, Andreas; ZIMMERMANN, Josef et al.American journal of kidney diseases. 2004, Vol 43, Num 3, pp 538-543, issn 0272-6386, 6 p.Article

Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndromeSUTAJOVA, Markéta; NEUKIRCHEN, Ursula; MEINECKE, Peter et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 5, pp 883-892, issn 0888-7543, 10 p.Article

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaCHAKAROVA, Christina F; HIMS, Matthew M; ROSENBERG, Thomas et al.Human molecular genetics (Print). 2002, Vol 11, Num 1, pp 87-92, issn 0964-6906Article

Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis PigmentosaLANGMANN, Thomas; DI GIOIA, Silvio Alessandro; ARSENIJEVIC, Yvan et al.American journal of human genetics. 2010, Vol 87, Num 3, pp 376-381, issn 0002-9297, 6 p.Article

Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene MutationsRENNER, Agnes B; FIEBIG, Britta S; WEBER, Bernhard H. F et al.American journal of ophthalmology. 2009, Vol 147, Num 3, pp 518-530, issn 0002-9394, 13 p.Article

Trace-based Just-in-Time Type Specialization for Dynamic LanguagesGAL, Andreas; EICH, Brendan; RUDERMAN, Jesse et al.ACM SIGPLAN notices. 2009, Vol 44, Num 6, pp 465-478, issn 1523-2867, 14 p.Conference Paper

Mutations of the mitochondrial holocytochrome c-Type synthase in X-Linked dominant microphthalmia with linear skin defects syndromeWIMPLINGER, Isabella; MORLEO, Manuela; KUTSCHE, Kerstin et al.American journal of human genetics. 2006, Vol 79, Num 5, pp 878-889, issn 0002-9297, 12 p.Article

Novel mutations and repeated findings of mutations in familial Alzheimer diseaseFINCKH, Ulrich; KUSCHEL, Christian; GAL, Andreas et al.Neurogenetics (Oxford. Print). 2005, Vol 6, Num 2, pp 85-89, issn 1364-6745, 5 p.Article

Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer diseaseGÜNTHER, Claudia; VON HADELN, Kirsten; FINCKH, Ulrich et al.Neuroscience letters. 2004, Vol 369, Num 3, pp 219-223, issn 0304-3940, 5 p.Article

No mutation in the gene for noonan syndrome, PTPN11, in 18 patients with costello syndromeTRÖGER, Birte; KUTSCHE, Kerstin; STEFANOVA, Margarita et al.American journal of medical genetics. 2003, Vol 121A, Num 1, pp 82-84, issn 0148-7299, 3 p.Article

Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophyTHOMPSON, Debra A; YUN LI; MCHENRY, Christina L et al.Nature genetics. 2001, Vol 28, Num 2, pp 123-124, issn 1061-4036Article

Hydrops fetalis in three male fetuses of a female with incontinentia pigmentiDUFKE, Andreas; VOLLMER, Brigitte; KENDZIORRA, Heidemarie et al.Prenatal diagnosis. 2001, Vol 21, Num 12, pp 1019-1021, issn 0197-3851Article