| Prediction of Causal Candidate Genes in Coronary Artery Disease Loci I Brænne, M Civelek, B Vilne, A Di Narzo, AD Johnson, Y Zhao, B Reiz, ... Arteriosclerosis, thrombosis, and vascular biology 35 (10), 2207-2217, 2015 | 122* | 2015 |
| Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction I Brænne, M Kleinecke, B Reiz, E Graf, T Strom, T Wieland, M Fischer, ... European Journal of Human Genetics 24 (2), 191-197, 2016 | 97 | 2016 |
| Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes I Parenti, ME Teresa-Rodrigo, J Pozojevic, SR Gil, I Bader, D Braunholz, ... Human Genetics 136 (3), 307-320, 2017 | 83 | 2017 |
| 46, XY Gonadal Dysgenesis due to a Homozygous Mutation in Desert Hedgehog (DHH) Identified by Exome Sequencing R Werner, H Merz, W Birnbaum, L Marshall, T Schröder, B Reiz, ... The Journal of Clinical Endocrinology & Metabolism 100 (7), E1022-E1029, 2015 | 83 | 2015 |
| A positive genotype–phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo‐pseudohypoparathyroidism and 33 newly identified … S Thiele, R Werner, J Grötzinger, B Brix, P Staedt, D Struve, B Reiz, ... Molecular genetics & genomic medicine 3 (2), 111-120, 2015 | 60 | 2015 |
| New NR5A1 mutations and phenotypic variations of gonadal dysgenesis R Werner, I Mönig, R Lünstedt, L Wünsch, C Thorns, B Reiz, A Krause, ... PLoS One 12 (5), e0176720, 2017 | 48 | 2017 |
| Hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics D Braunholz, C Obieglo, I Parenti, J Pozojevic, J Eckhold, B Reiz, ... Human mutation 36 (1), 26-29, 2015 | 36 | 2015 |
| Alveolar macrophages in early stage COPD show functional deviations with properties of impaired immune activation K Baßler, W Fujii, TS Kapellos, E Dudkin, N Reusch, A Horne, B Reiz, ... Frontiers in Immunology, 3795, 0 | 30* | |
| Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia I Brænne, B Reiz, A Medack, M Kleinecke, M Fischer, S Tuna, ... BMC cardiovascular disorders 14 (1), 1, 2014 | 27 | 2014 |
| A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A TJ Demal, M Heise, B Reiz, D Dogra, I Brænne, H Reichenspurner, ... Scientific Reports 9 (1), 2959, 2019 | 17 | 2019 |
| Novel insights into 46, XY disorders of sex development due to NR5A1 gene mutation R Werner, I Mönig, J August, C Freiberg, R Lünstedt, B Reiz, L Wünsch, ... Sexual Development 9 (5), 260-268, 2015 | 17 | 2015 |
| A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors. I Brænne, C Willenborg, V Tragante, T Kessler, L Zeng, B Reiz, ... Scientific reports 7 (1), 10252, 2017 | 16 | 2017 |
| Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression R Hollstein, B Reiz, L Kötter, A Richter, S Schaake, K Lohmann, FJ Kaiser Human molecular genetics 26 (15), 2975-2983, 2017 | 16 | 2017 |
| Analysis of candidate genes for cleft lip±cleft palate using murine single-cell expression data A Siewert, B Reiz, C Krug, J Heggemann, E Mangold, H Dickten, ... Frontiers in Cell and Developmental Biology 11, 1091666, 2023 | 5 | 2023 |
| Die künstliche Intelligenz in der Einzelzellgenomik H Dickten, C Kratsch, B Reiz Gefässchirurgie 24 (7), 523-530, 2019 | 3 | 2019 |
| Human variation in population-wide gene expression data predicts gene perturbation phenotype L Bonaguro, J Schulte-Schrepping, C Carraro, LL Sun, B Reiz, I Gemünd, ... Iscience 25 (11), 2022 | 1 | 2022 |
| Pleiotropic molecular targets of coxibs reveals novel genomic loci conferring coronary artery disease risk I Brænne, C Willenborg, B Reiz, L Zeng, T Meitinger, NJ Samani, ... Atherosclerosis 252, e252-e253, 2016 | 1 | 2016 |
| Genomatics: Computational Approaches to Unravel the Genetics Underlying Cardiological Traits B Reiz Universität zu Lübeck, 2017 | | 2017 |
| Making Genomes Visible B Reiz, J Erdmann, C Rehmann-Sutter Genetic Transparency? Ethical and Social Implications of Next Generation …, 2016 | | 2016 |
| A new next generation sequencing panel for mutational screening of putative genes causing 46, XY disorders of sex development (DSD) S Flieger, B Brix, D Braunholz, B Reiz, FJ Kaiser, O Hiort, R Werner Experimental and Clinical Endocrinology & Diabetes 123 (03), P11_01, 2015 | | 2015 |
Ingrid BrænneBoehringer Ingelheim在 boehringer-ingelheim.com 的电子邮件经过验证
