Sallinen RJ - Search Results

1

Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults.

Sallinen RJ, Dethlefsen O, Ruotsalainen S, Mills RD, Miettinen TA, Jääskeläinen TE, Lundqvist A, Kyllönen E, Kröger H, Karppinen JI, Lamberg-Allardt C, Viljakainen H, Kaunisto MA, Kallioniemi O. Sallinen RJ, et al. J Nutr. 2021 Feb 1;151(2):281-292. doi: 10.1093/jn/nxaa391. J Nutr. 2021. PMID: 33382404 Free article.

2

Novel susceptibility locus at 22q11 for diabetic nephropathy in type 1 diabetes.

Wessman M, Forsblom C, Kaunisto MA, Söderlund J, Ilonen J, Sallinen R, Hiekkalinna T, Parkkonen M, Maxwell AP, Tarnow L, Parving HH, Hadjadj S, Marre M, Peltonen L, Groop PH; FinnDiane Study Group. Wessman M, et al. PLoS One. 2011;6(9):e24053. doi: 10.1371/journal.pone.0024053. Epub 2011 Sep 1. PLoS One. 2011. PMID: 21909410 Free PMC article.

3

Multiomics and digital monitoring during lifestyle changes reveal independent dimensions of human biology and health.

Marabita F, James T, Karhu A, Virtanen H, Kettunen K, Stenlund H, Boulund F, Hellström C, Neiman M, Mills R, Perheentupa T, Laivuori H, Helkkula P, Byrne M, Jokinen I, Honko H, Kallonen A, Ermes M, Similä H, Lindholm M, Widén E, Ripatti S, Perälä-Heape M, Engstrand L, Nilsson P, Moritz T, Miettinen T, Sallinen R, Kallioniemi O. Marabita F, et al. Cell Syst. 2022 Mar 16;13(3):241-255.e7. doi: 10.1016/j.cels.2021.11.001. Epub 2021 Dec 1. Cell Syst. 2022. PMID: 34856119 Free article.

4

Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy.

Kaunisto MA, Sjölind L, Sallinen R, Pettersson-Fernholm K, Saraheimo M, Fröjdö S, Forsblom C, Fagerudd J, Hansen TK, Flyvbjerg A, Wessman M, Groop PH; FinnDiane Study Group. Kaunisto MA, et al. Diabetes. 2009 Jul;58(7):1710-4. doi: 10.2337/db08-1495. Epub 2009 Apr 14. Diabetes. 2009. PMID: 19366862 Free PMC article.

5

Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension.

Sallinen R, Kaunisto MA, Forsblom C, Thomas M, Fagerudd J, Pettersson-Fernholm K, Groop PH, Wessman M; Finnish Diabetic Nephropathy Study Group. Sallinen R, et al. Ann Med. 2010 May 6;42(4):296-304. doi: 10.3109/07853891003777109. Ann Med. 2010. PMID: 20429798

6

Individual and stable autoantibody repertoires in healthy individuals.

Neiman M, Hellström C, Just D, Mattsson C, Fagerberg L, Schuppe-Koistinen I, Gummesson A, Bergström G, Kallioniemi O, Achour A, Sallinen R, Uhlén M, Nilsson P. Neiman M, et al. Autoimmunity. 2019 Feb;52(1):1-11. doi: 10.1080/08916934.2019.1581774. Epub 2019 Mar 5. Autoimmunity. 2019. PMID: 30835561 Clinical Trial.

7

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

Kaunisto MA, Harno H, Kallela M, Somer H, Sallinen R, Hämäläinen E, Miettinen PJ, Vesa J, Orpana A, Palotie A, Färkkilä M, Wessman M. Kaunisto MA, et al. Neurogenetics. 2004 Feb;5(1):69-73. doi: 10.1007/s10048-003-0161-0. Epub 2003 Oct 7. Neurogenetics. 2004. PMID: 14530926

8

DDOST, PRKCSH and LGALS3, which encode AGE-receptors 1, 2 and 3, respectively, are not associated with diabetic nephropathy in type 1 diabetes.

Hoverfelt A, Sallinen R, Söderlund JM, Forsblom C, Pettersson-Fernholm K, Parkkonen M, Groop PH, Wessman M; FinnDiane Study Group. Hoverfelt A, et al. Diabetologia. 2010 Sep;53(9):1903-7. doi: 10.1007/s00125-010-1771-3. Epub 2010 May 21. Diabetologia. 2010. PMID: 20490454

9

Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization.

Sallinen R, Kuang W, Engvall E, Palotie A, Wessman M, Horelli-Kuitunen N. Sallinen R, et al. Cytogenet Cell Genet. 1999;87(3-4):195-6. doi: 10.1159/000015464. Cytogenet Cell Genet. 1999. PMID: 10702665 No abstract available.

10

Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K(+)-Cl(-) cotransporter (KCC2) defines a new region of conserved homology.

Sallinen R, Tornberg J, Putkiranta M, Horelli-Kuitunen N, Airaksinen MS, Wessman M. Sallinen R, et al. Cytogenet Cell Genet. 2001;94(1-2):67-70. doi: 10.1159/000048785. Cytogenet Cell Genet. 2001. PMID: 11701957

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