|
| 34492681 | Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development. | Blood Adv | 2021 |
| 34492681 | Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development. | Blood Adv | 2021 |
| 32186706 | The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology. | Hum Mol Genet | 2020 |
| 32186706 | The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology. | Hum Mol Genet | 2020 |
| 31996359 | Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1. | Dis Model Mech | 2020 |
| 31996359 | Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1. | Dis Model Mech | 2020 |
| 30540754 | Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility. | PLoS Genet | 2018 |
| 30540754 | Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility. | PLoS Genet | 2018 |
| 28040780 | Highly Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection. | G3 (Bethesda) | 2017 |
| 28040780 | Highly Efficient Cpf1-Mediated Gene Targeting in Mice Following High Concentration Pronuclear Injection. | G3 (Bethesda) | 2017 |
| 26841305 | Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia. | Hum Mutat | 2016 |
| 26841305 | Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia. | Hum Mutat | 2016 |
| 27258160 | CRISPR-Mediated Triple Knockout of SLAMF1, SLAMF5 and SLAMF6 Supports Positive Signaling Roles in NKT Cell Development. | PLoS One | 2016 |
| 27258160 | CRISPR-Mediated Triple Knockout of SLAMF1, SLAMF5 and SLAMF6 Supports Positive Signaling Roles in NKT Cell Development. | PLoS One | 2016 |
| 25865046 | A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase. | Gastroenterology | 2015 |
| 25865046 | A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase. | Gastroenterology | 2015 |
| 26048245 | High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9. | Genome Res | 2015 |
| 26048245 | High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9. | Genome Res | 2015 |
| 22710270 | Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease. | Mol Psychiatry | 2013 |
| 22948022 | Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis. | Eur J Hum Genet | 2013 |
| 22710270 | Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease. | Mol Psychiatry | 2013 |
| 22948022 | Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis. | Eur J Hum Genet | 2013 |
| 22264778 | Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering. | Mol Genet Metab | 2012 |
| 22750566 | GWAS reveals new recessive loci associated with non-syndromic facial clefting. | Eur J Med Genet | 2012 |
| 22264778 | Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering. | Mol Genet Metab | 2012 |
| 22750566 | GWAS reveals new recessive loci associated with non-syndromic facial clefting. | Eur J Med Genet | 2012 |
| 21207418 | Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22. | Int J Cancer | 2011 |
| 21207418 | Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22. | Int J Cancer | 2011 |
| 19147536 | Loss-of-function fibroblast growth factor receptor-2 mutations in melanoma. | Mol Cancer Res | 2009 |
| 19147536 | Loss-of-function fibroblast growth factor receptor-2 mutations in melanoma. | Mol Cancer Res | 2009 |
| 16230383 | Gene expression profiling of human sarcomas: insights into sarcoma biology. | Cancer Res | 2005 |
| 16230383 | Gene expression profiling of human sarcomas: insights into sarcoma biology. | Cancer Res | 2005 |
| 15048078 | Microarray expression profiling in melanoma reveals a BRAF mutation signature. | Oncogene | 2004 |
| 15048078 | Microarray expression profiling in melanoma reveals a BRAF mutation signature. | Oncogene | 2004 |
| 12447372 | High frequency of BRAF mutations in nevi. | Nat Genet | 2003 |
| 12447372 | High frequency of BRAF mutations in nevi. | Nat Genet | 2003 |