共 50 条
- [1] From cytogenetics to cytogenomics whole genome sequencing as a comprehensive genetic test in rare disease diagnosticsMOLECULAR CYTOGENETICS, 2019, 12Eisfeldt, Jesper论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLundin, Johanna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenPettersson, Maria论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenKvarnung, Malin论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLieden, Agne论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenSahlin, Ellika论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLagerstedt, Kristina论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenMartin, Marcel论文数: 0 引用数: 0 h-index: 0机构: Nbis, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenYgberg, Sofia论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Inst Womens & Childrens Hlth, Neuropediat Unit, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenBjerin, Olof论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Inst Womens & Childrens Hlth, Neuropediat Unit, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenStranneheim, Henrik论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenWedell, Anna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenNordenskjold, Magnus论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenSoller, Maria Johansson论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenNordgren, Ann论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenWirta, Valtteri论文数: 0 引用数: 0 h-index: 0机构: Kth Royal Inst Technol, Sch Engn Sci Chem Biotechnol & Hlth, Scilifelab, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenNilsson, Daniel论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLindstrand, Anna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden
- [2] From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disabilityGenome Medicine, 11Anna Lindstrand论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsJesper Eisfeldt论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsMaria Pettersson论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsClaudia M. B. Carvalho论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsMalin Kvarnung论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsGiedre Grigelioniene论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsBritt-Marie Anderlid论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsOlof Bjerin论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsPeter Gustavsson论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsAnna Hammarsjö论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsPatrik Georgii-Hemming论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsErik Iwarsson论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsMaria Johansson-Soller论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsKristina Lagerstedt-Robinson论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsAgne Lieden论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsMåns Magnusson论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsMarcel Martin论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsHelena Malmgren论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsMagnus Nordenskjöld论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsAmeli Norling论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsEllika Sahlin论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsHenrik Stranneheim论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsEmma Tham论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsJosephine Wincent论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsSofia Ygberg论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsAnna Wedell论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsValtteri Wirta论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsAnn Nordgren论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsJohanna Lundin论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical GeneticsDaniel Nilsson论文数: 0 引用数: 0 h-index: 0机构: Karolinska University Hospital,Department of Clinical Genetics
- [3] From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disabilityGENOME MEDICINE, 2019, 11 (01)Lindstrand, Anna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenEisfeldt, Jesper论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Inst, Sci Life Lab, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenPettersson, Maria论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenCarvalho, Claudia M. B.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenKvarnung, Malin论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden论文数: 引用数: h-index:机构:Anderlid, Britt-Marie论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenBjerin, Olof论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Dept Womens & Childrens Hlth, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenGustavsson, Peter论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenHammarsjo, Anna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenGeorgii-Hemming, Patrik论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenIwarsson, Erik论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenJohansson-Soller, Maria论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLagerstedt-Robinson, Kristina论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLieden, Agne论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenMagnusson, Mans论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Sci Life Lab, Stockholm, Sweden Karolinska Univ Hosp, Ctr Inherited Metab Dis, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden论文数: 引用数: h-index:机构:Malmgren, Helena论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenNordenskjold, Magnus论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden论文数: 引用数: h-index:机构:Sahlin, Ellika论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenStranneheim, Henrik论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Ctr Inherited Metab Dis, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenTham, Emma论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenWincent, Josephine论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenYgberg, Sofia论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Ctr Inherited Metab Dis, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenWedell, Anna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Univ Hosp, Ctr Inherited Metab Dis, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenWirta, Valtteri论文数: 0 引用数: 0 h-index: 0机构: KTH Royal Inst Technol, Sch Engn Sci Chem Biotechnol & Hlth, Sci Life Lab, Stockholm, Sweden Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Sci Life Lab, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenNordgren, Ann论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenLundin, Johanna论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Karolinska Univ Hosp, Dept Clin Genet, Stockholm, SwedenNilsson, Daniel论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden Karolinska Inst, Ctr Mol Med, Stockholm, Sweden Karolinska Inst, Sci Life Lab, Stockholm, Sweden Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden
- [4] Recommendations for whole genome sequencing in diagnostics for rare diseasesEuropean Journal of Human Genetics, 2022, 30 : 1017 - 1021Erika Souche论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenSergi Beltran论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenErwin Brosens论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenJohn W. Belmont论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMagdalena Fossum论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenOlaf Riess论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenChristian Gilissen论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenAmin Ardeshirdavani论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenGunnar Houge论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMarielle van Gijn论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenJill Clayton-Smith论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMatthis Synofzik论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenNicole de Leeuw论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenZandra C. Deans论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenYasemin Dincer论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenSebastian H. Eck论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenSaskia van der Crabben论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMeena Balasubramanian论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenHolm Graessner论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMarc Sturm论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenHelen Firth论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenAlessandra Ferlini论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenRima Nabbout论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenElfride De Baere论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenThomas Liehr论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMilan Macek论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenGert Matthijs论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenHans Scheffer论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenPeter Bauer论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenHelger G. Yntema论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU LeuvenMarjan M. Weiss论文数: 0 引用数: 0 h-index: 0机构: Gasthuisberg,Center for Human Genetics, KU Leuven
- [5] Recommendations for whole genome sequencing in diagnostics for rare diseasesEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (09) : 1017 - 1021Souche, Erika论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium论文数: 引用数: h-index:机构:Brosens, Erwin论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC Univ Med Ctr, Dept Clin Genet, Sophia Childrens Hosp, Rotterdam, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumBelmont, John W.论文数: 0 引用数: 0 h-index: 0机构: Illumina Inc, Baylor Coll Med, Dept Mol & Human Genet, Houston, TX USA Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumFossum, Magdalena论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Fac Hlth & Med Sci, Rigshosp, Dept Pediat Surg, Copenhagen, Denmark Karolinska Inst, Dept Womens & Childrens Hlth, Stockholm, Sweden Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumRiess, Olaf论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumGilissen, Christian论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen Med Ctr, Radboud Inst Mol Life Sci, NL-6525 GA Nijmegen, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumArdeshirdavani, Amin论文数: 0 引用数: 0 h-index: 0机构: Agilent Technol, Diagnost & Genom Grp, Leuven, Belgium Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumHouge, Gunnar论文数: 0 引用数: 0 h-index: 0机构: Haukeland Hosp, Dept Med Genet, N-5021 Bergen, Norway Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Synofzik, Matthis论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Hertie Inst Clin Brain Res, Tubingen, Germany German Ctr Neurodegenerat Dis DZNE, Tubingen, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgiumde Leeuw, Nicole论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen Med Ctr, Dept Human Genet, NL-6525 GA Nijmegen, Netherlands Radboud Univ Nijmegen Med Ctr, Donders Ctr Cognit Neurosci, Nijmegen, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumDeans, Zandra C.论文数: 0 引用数: 0 h-index: 0机构: NHS Lothian, Genom Qual Assessment, Edinburgh, Midlothian, Scotland Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumDincer, Yasemin论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Lehrstuhl Sozialpadiatrie, Munich, Germany Zentrum Humangenet & Lab Diagnost MVZ, Martinsried, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumEck, Sebastian H.论文数: 0 引用数: 0 h-index: 0机构: MVZ Martinsried GmbH, Martinsried, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgiumvan eer Crabben, Saskia论文数: 0 引用数: 0 h-index: 0机构: Amsterdam Univ Med Ctr, Dept Clin Genet, Locat AMC, Amsterdam, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumBalasubramanian, Meena论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens NHS Fdn Trust, Highly Specialised Osteogenesis Imperfecta Serv, Sheffield, S Yorkshire, England Sheffield Childrens NHS Fdn Trust, Sheffield Clin Genet Serv, Sheffield, S Yorkshire, England Univ Sheffield, Dept Oncol & Metab, Sheffield, S Yorkshire, England Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumGraessner, Holm论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Tubingen, Inst Med Genet & Appl Genom, Calwerstr 7, D-72076 Tubingen, Germany Univ Hosp Tubingen, Ctr Rare Dis, Calwerstr 7, D-72076 Tubingen, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumSturm, Marc论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Med Genet & Appl Genom, Tubingen, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumFirth, Helen论文数: 0 引用数: 0 h-index: 0机构: Cambridge Univ Hosp, Dept Clin Genet, Box 134, Cambridge, England Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium论文数: 引用数: h-index:机构:Nabbout, Rima论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Hop Necker Enfants Malad, AP HP, Inst Imagine INSERM UMR 1163,Pediat Neurol Refere, Paris, France Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Macek, Milan论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Fac Med 2, Dept Biol & Med Genet, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumMatthijs, Gert论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumScheffer, Hans论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen Med Ctr, Dept Human Genet, POB 9101, NL-6500 HB Nijmegen, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumBauer, Peter论文数: 0 引用数: 0 h-index: 0机构: CENTOGENE GmbH, Strande 7, D-18055 Rostock, Germany Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumYntema, Helger G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen Med Ctr, Dept Human Genet, POB 9101, NL-6500 HB Nijmegen, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, BelgiumWeiss, Marjan M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen Med Ctr, Dept Human Genet, POB 9101, NL-6500 HB Nijmegen, Netherlands Katholieke Univ Leuven, Lab Mol Diag, Gasthuisberg, Ctr Human Genet, Leuven, Belgium
- [6] Accurate Whole Genome Sequencing as the Ultimate Genetic TestCLINICAL CHEMISTRY, 2015, 61 (01) : 305 - 306Drmanac, Radoje论文数: 0 引用数: 0 h-index: 0机构: Complete Genom Inc, Mountain View, CA USA BGI Shenzhen, Shenzhen, Peoples R China Complete Genom Inc, Mountain View, CA USAPeters, Brock A.论文数: 0 引用数: 0 h-index: 0机构: Complete Genom Inc, Mountain View, CA USA BGI Shenzhen, Shenzhen, Peoples R China Complete Genom Inc, Mountain View, CA USAChurch, George M.论文数: 0 引用数: 0 h-index: 0机构: Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA Complete Genom Inc, Mountain View, CA USAReid, Clifford A.论文数: 0 引用数: 0 h-index: 0机构: Complete Genom Inc, Mountain View, CA USA Complete Genom Inc, Mountain View, CA USAXu, Xun论文数: 0 引用数: 0 h-index: 0机构: BGI Shenzhen, Shenzhen, Peoples R China Complete Genom Inc, Mountain View, CA USA
- [7] Whole genome sequencing - a challenge for genome diagnosticsGYNAKOLOGE, 2014, 47 (08): : 565 - 567Streubel, B.论文数: 0 引用数: 0 h-index: 0机构: Med Univ Wien, Univ Klin Frauenheilkunde, Wahringer Gurtel 18-20, A-1090 Vienna, Austria Med Univ Wien, Univ Klin Frauenheilkunde, Wahringer Gurtel 18-20, A-1090 Vienna, Austria
- [8] Comprehensive Genetic Landscape of Uveal Melanoma by Whole-Genome SequencingAMERICAN JOURNAL OF HUMAN GENETICS, 2016, 99 (05) : 1190 - 1198Royer-Bertrand, Beryl论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, Switzerland Univ Lausanne Hosp, Ctr Mol Dis, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandTorsello, Matteo论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne Hosp, Inst Pathol, Expt Pathol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandRimoldi, Donata论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne Hosp, Inst Pathol, Expt Pathol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandEl Zaoui, Ikram论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandCisarova, Katarina论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandPescini-Gobert, Rosanna论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandRaynaud, Franck论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Dept Computat Biol, Computat Syst Oncol, CH-1011 Lausanne, Switzerland Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandZografos, Leonidas论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Jules Gonin Eye Hosp, Dept Ophthalmol, Fdn Asile Aveugles, CH-1004 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandSchalenbourg, Ann论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Jules Gonin Eye Hosp, Dept Ophthalmol, Fdn Asile Aveugles, CH-1004 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandSpeiser, Daniel论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne Hosp, Inst Pathol, Expt Pathol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, Switzerland论文数: 引用数: h-index:机构:Vallat, Laureen论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Jules Gonin Eye Hosp, Dept Ophthalmol, Fdn Asile Aveugles, CH-1004 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandKlein, Robert论文数: 0 引用数: 0 h-index: 0机构: Formerly Complete Genom, Mountain View, CA 94043 USA Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandLeyvraz, Serge论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne Hosp, Dept Oncol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandCiriello, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Dept Computat Biol, Computat Syst Oncol, CH-1011 Lausanne, Switzerland Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandRiggi, Nicolo论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne Hosp, Inst Pathol, Expt Pathol, CH-1011 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, SwitzerlandMoulin, Alexandre P.论文数: 0 引用数: 0 h-index: 0机构: Univ Lausanne, Jules Gonin Eye Hosp, Dept Ophthalmol, Fdn Asile Aveugles, CH-1004 Lausanne, Switzerland Univ Lausanne, Unit Med Genet, Dept Computat Biol, CH-1011 Lausanne, Switzerland论文数: 引用数: h-index:机构:
- [9] Genetic Counseling and Genome Sequencing in Pediatric Rare DiseaseCOLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2020, 10 (03):Elliott, Alison M.论文数: 0 引用数: 0 h-index: 0机构: Univ British Columbia, Dept Med Genet, Columbia, BC V6H 3N1, Canada BC Childrens Hosp Res Inst, Columbia, BC V6H 3N1, Canada BC Womens Hlth Res Inst, Columbia, BC V6H 3N1, Canada Prov Med Genet Program, Columbia, BC V6H 3N1, Canada Univ British Columbia, Dept Med Genet, Columbia, BC V6H 3N1, Canada
- [10] Clinical Utility of Whole Genome Sequencing for Undiagnosed Rare Genetic DisordersJOURNAL OF THE LIAQUAT UNIVERSITY OF MEDICAL AND HEALTH SCIENCES, 2021, 20 (01): : 1 - 2Awan, Muhammad Qasim论文数: 0 引用数: 0 h-index: 0机构: Govt Coll Univ, Dept Bioinfolinat & Biotechnol, Faisalabad, Pakistan Govt Coll Univ, Dept Bioinfolinat & Biotechnol, Faisalabad, Pakistan