E-LIB Suche - Ergebnisse für: Nikopensius, Tiit

1

Genome-wide meta-analysis identifies novel loci conferring ..:

Teder-Laving, Maris ; Kals, Mart ; Reigo, Anu...
European Journal of Human Genetics. , 2023

Link: https://doi.org/10.1038/..

2

Correction: Genome-wide meta-analysis identifies novel loci..:

Teder-Laving, Maris ; Kals, Mart ; Reigo, Anu...
European Journal of Human Genetics. , 2023

Link: https://doi.org/10.1038/..

3

Precise, Genotype-First Breast Cancer Prevention: Experienc..:

Jürgens, Hannes ; Roht, Laura ; Leitsalu, Liis...
Frontiers in Genetics. 13 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

4

Do Biobank Recall Studies Matter? Long-Term Follow-Up of Re..:

Nurm, Miriam ; Reigo, Anu ; Nõukas, Margit...
Frontiers in Genetics. 13 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

5

Lessons learned during the process of reporting individual ..:

Leitsalu, Liis ; Reigo, Anu ; Palover, Marili...
European Journal of Human Genetics. 31 (2022) 9 - p. 1048-1056 , 2022

Link: https://doi.org/10.1038/..

6

Association analysis of juvenile idiopathic arthritis genet..:

Nikopensius, Tiit ; Niibo, Priit ; Haller, Toomas...
Clinical Rheumatology. 40 (2021) 10 - p. 4157-4165 , 2021

Link: https://doi.org/10.1007/..

7

Genotype-first approach to the detection of hereditary brea..:

Leitsalu, Liis ; Palover, Marili ; Sikka, Timo Tõnis...
European Journal of Human Genetics. 29 (2020) 3 - p. 471-481 , 2020

Link: https://doi.org/10.1038/..

8

Recall by genotype and cascade screening for familial hyper..:

Alver, Maris ; Palover, Marili ; Saar, Aet...
Genetics in Medicine. 21 (2019) 5 - p. 1173-1180 , 2019

Link: https://doi.org/10.1038/..

9

Exome analysis in an Estonian multiplex family with neural ..:

Pappa, Liina ; Kals, Mart ; Kivistik, Paula Ann...
Child's Nervous System. 33 (2017) 9 - p. 1575-1581 , 2017

Link: https://doi.org/10.1007/..

10

Contemporary management of TMJ involvement in JIA patients ..:

Niibo, Priit ; Pruunsild, Chris ; Voog-Oras, Ülle...
EPMA Journal. 7 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

11

De novo exonic mutation in MYH7 gene leading to exon skippi..:

Pajusalu, Sander ; Talvik, Inga ; Noormets, Klari...
Neuromuscular Disorders. 26 (2016) 3 - p. 236-239 , 2016

Link: https://doi.org/10.1016/..

12

Whole-exome sequencing identifies de novo mutation in the C..:

Maasalu, Katre ; Nikopensius, Tiit ; Kõks, Sulev...
Human Genomics. 9 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

13

Are Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymo..:

Lorenz, Anna-Liisa ; Kahre, Tiina ; Mihailov, Evelin...
Journal of Biomedical Science and Engineering. 7 (2014) 8 - p. 464-472 , 2014

Link: https://doi.org/10.4236/..

14

De NovoSCN8A Mutation Identified by Whole-Exome Sequencing ..:

Vaher, Ulvi ; Nõukas, Margit ; Nikopensius, Tiit...
Journal of Child Neurology. 29 (2013) 12 - p. NP202-NP206 , 2013

Link: https://doi.org/10.1177/..

15

MTHFR and MSX1 contribute to the risk of nonsyndromic cleft..:

Jagomägi, Triin ; Nikopensius, Tiit ; Krjutškov, Kaarel...
European Journal of Oral Sciences. 118 (2010) 3 - p. 213-220 , 2010

Link: https://doi.org/10.1111/..