Genomewide scans of complex human diseases : True linkage is hard to findALTMÜLLER, Janine; PALMER, Lyle J; FISCHER, Guido et al.American journal of human genetics. 2001, Vol 69, Num 5, pp 936-950, issn 0002-9297Article

Genome-wide association study of lung function decline in adults with and without asthmaIMBODEN, Medea; BOUZIGON, Emmanuelle; NADIF, Rachel et al.Journal of allergy and clinical immunology. 2012, Vol 129, Num 5, pp 1218-1228, issn 0091-6749, 11 p.Article

Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeWEBER, Stefanie; THIELE, Holger; STUART, Helen M et al.American journal of human genetics. 2011, Vol 89, Num 5, pp 668-674, issn 0002-9297, 7 p.Article

Nonsense Mutations in SMPX, Encoding a Protein Responsive to Physical Force, Result in X-Chromosomal Hearing LossHUEBNER, Antje K; GANDIA, Marta; MORENO, Felipe et al.American journal of human genetics. 2011, Vol 88, Num 5, pp 621-627, issn 0002-9297, 7 p.Article

Association of ALPL and ENPP1 gene polymorphisms with bone strength related skeletal traits in a Chuvashian populationERMAKOV, Sergey; MOHAMMAD REZA TOLIAT; COHEN, Zvi et al.Bone (New York, NY). 2010, Vol 46, Num 5, pp 1244-1250, issn 8756-3282, 7 p.Article

High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseasesHERBON, Nicole; WERNER, Monika; BONIFACIO, Ezio et al.Genomics (San Diego, Calif.). 2003, Vol 81, Num 5, pp 510-518, issn 0888-7543, 9 p.Article

Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cellsNOETEL, Andrea; ELFIMOVA, Natalia; DIENES, Hans Peter et al.Journal of hepatology. 2013, Vol 58, Num 2, pp 335-341, issn 0168-8278, 7 p.Article

Lifestyle transitions in plant pathogenic Colletotrichum fungi deciphered by genome and transcriptome analysesO'CONNELL, Richard J; THON, Michael R; ALTMÜLLER, Janine et al.Nature genetics. 2012, Vol 44, Num 9, pp 1060-1065, issn 1061-4036, 6 p.Article

A genome-wide linkage scan for 25-OH-D₃ and 1,25-(OH)₂-D₃ serum levels in asthma familiesWJST, Matthias; ALTMÜLLER, Janine; BRAIG, Christine et al.Journal of steroid biochemistry and molecular biology. 2007, Vol 103, Num 3-5, pp 799-802, issn 0960-0760, 4 p.Conference Paper

A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal FunctionHUSSAIN, Muhammad Sajid; BAIG, Shahid Mahmood; FROMMOLT, Peter et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 871-878, issn 0002-9297, 8 p.Article

Attenuated BMP1 Function Compromises Osteogenesis, Leading to Bone Fragility in Humans and ZebrafishASHARANI, P. V; KEUPP, Katharina; SONNTAG, Carmen et al.American journal of human genetics. 2012, Vol 90, Num 4, pp 661-674, issn 0002-9297, 14 p.Article

Integrative genome analyses identify key somatic driver mutations of small-cell lung cancerPEIFER, Martin; FERNANDEZ-CUESTA, Lynnette; MENON, Roopika et al.Nature genetics. 2012, Vol 44, Num 10, pp 1104-1110, issn 1061-4036, 7 p.Article

Deficiency for the Ubiquitin Ligase UBE3B in a Blepharophimosis-Ptosis-Intellectual-Disability SyndromeBASEL-VANAGAITE, Lina; DALLAPICCOLA, Bruno; ABRAMOWICZ, Marc et al.American journal of human genetics. 2012, Vol 91, Num 6, pp 998-1010, issn 0002-9297, 13 p.Article

Association of the interleukin-1 receptor antagonist gene with asthmaHENNING GOHLKE; ILLIG, Thomas; BONER, Attilio et al.American journal of respiratory and critical care medicine. 2004, Vol 169, Num 11, pp 1217-1223, issn 1073-449X, 7 p.Article

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGUDBJARTSSON, Daniel F; BJORNSDOTTIR, Unnur S; WILLIAMS, Carolyn et al.Nature genetics. 2009, Vol 41, Num 3, pp 342-347, issn 1061-4036, 6 p.Article