Publication list - Publika - Scientific publications from Oslo University Hospital

Publications by Marissa LeBlanc

34 publications found

Original articles

Rehbinder EM, Wärnberg Gerdin S, Hoyer A, Bradley M, Lødrup Carlsen KC, Granum B, Hedlin G, Jonassen CM, Leblanc M, Nordlund B, Rudi K, Skjerven HO, Staff AC, Vettukattil R, Söderhäll C (2024)
Frequent oil-baths and skin barrier during infancy in the PreventADALL study
Br J Dermatol (in press)
DOI 10.1093/bjd/ljae091, PubMed 38446755

Choi HJ, LeBlanc M, Moger TA, Valberg M, Page CM, Aamodt G, Næss Ø (2023)
Geographical variation in cardiovascular disease mortality in Norway: The role of life course socioeconomic position and parental health
Health Place, 83, 103095
DOI 10.1016/j.healthplace.2023.103095, PubMed 37659155

Saunders CM, Rehbinder EM, Carlsen KCL, Jonassen CM, LeBlanc M, Nordlund B, Skjerven HO, Söderhäll C, Vettukattil R, Carlsen MH (2023)
Feeding Practices and Dietary Diversity in the First Year of Life: PreventADALL, a Scandinavian Randomized Controlled Trial and Birth Cohort Study
J Nutr, 153 (8), 2463-2471
DOI 10.1016/j.tjnut.2023.06.015, PubMed 37336319

Hilde K, Gudmundsdóttir HK, Bains KES, Carlsen KCL, Färdig M, Jonassen CM, Kreyberg I, LeBlanc M, Nordlund B, Rehbinder EM, Roland MCP, Skjerven HO, Staff AC, Vettukattil R, Haugen G (2023)
Third trimester fetal lung volume, thoracic circumference, and early infant lung function
Pediatr Pulmonol, 58 (7), 2050-2058
DOI 10.1002/ppul.26431, PubMed 37098847

Hoel ST, Wiik J, Carlsen KCL, Endre KMA, Gudmundsdóttir HK, Haugen G, Hoyer A, Jonassen CM, LeBlanc M, Nordlund B, Rudi K, Skjerven HO, Staff AC, Hedlin G, Söderhäll C, Vettukattil R, Aaneland H, Rehbinder EM (2023)
Birth mode is associated with development of atopic dermatitis in infancy and early childhood
J Allergy Clin Immunol Glob, 2 (3), 100104
DOI 10.1016/j.jacig.2023.100104, PubMed 37779526

Gudmundsdóttir HK, Carlsen OCL, Bains KES, Färdig M, Haugen G, Jonassen CM, LeBlanc M, Nordlund B, Rehbinder EM, Skjerven HO, Staff AC, Vettukattil R, Lødrup Carlsen KC (2022)
Infant lung function and maternal physical activity in the first half of pregnancy
ERJ Open Res, 8 (4)
DOI 10.1183/23120541.00172-2022, PubMed 36329799

Gudmundsdóttir HK, Hilde K, Bains KES, Färdig M, Haugen G, LeBlanc M, Nordhagen LS, Nordlund B, Rehbinder EM, Skjerven HO, Staff AC, Vettukattil R, Carlsen KCL (2022)
Fetal thoracic circumference in mid-pregnancy and infant lung function
Pediatr Pulmonol, 58 (1), 35-45
DOI 10.1002/ppul.26153, PubMed 36097818

Choi HJ, LeBlanc M, Moger TA, Valberg M, Aamodt G, Page CM, Tell GS, Næss Ø (2022)
Stroke survival and the impact of geographic proximity to family members: A population-based cohort study
Soc Sci Med, 309, 115252
DOI 10.1016/j.socscimed.2022.115252, PubMed 35988529

Vejrup K, Agnihotri N, Bere E, Schjølberg S, LeBlanc M, Hillesund ER, Øverby NC (2022)
Adherence to a healthy and potentially sustainable Nordic diet is associated with child development in The Norwegian Mother, Father and Child Cohort Study (MoBa)
Nutr J, 21 (1), 46
DOI 10.1186/s12937-022-00799-5, PubMed 35843945

Skjerven HO, Lie A, Vettukattil R, Rehbinder EM, LeBlanc M, Asarnoj A, Carlsen KH, Despriee ÅW, Färdig M, Gerdin SW, Granum B, Gudmundsdóttir HK, Haugen G, Hedlin G, Håland G, Jonassen CM, Landrø L, Mägi CO, Olsen IC, Rudi K, Saunders CM, Skram MK, Staff AC, Söderhäll C, Tedner SG et al. (2022)
Early food intervention and skin emollients to prevent food allergy in young children (PreventADALL): a factorial, multicentre, cluster-randomised trial
Lancet, 399 (10344), 2398-2411
DOI 10.1016/S0140-6736(22)00687-0, PubMed 35753340

LeBlanc M, Rueegg CS, Bekiroğlu N, Esterhuizen TM, Fagerland MW, Falk RS, Frøslie KF, Graf E, Heinze G, Held U, Holst R, Lange T, Mazumdar M, Myrberg IH, Posch M, Sergeant JC, Vach W, Vance EA, Weedon-Fekjaer H, Zucknick M (2022)
Statistical advising: Professional development opportunities for the biostatistician
Stat Med, 41 (5), 847-859
DOI 10.1002/sim.9290, PubMed 35194815

Lie A, Wärnberg Gerdin S, Skrindo I, Rehbinder EM, Jonassen CM, LeBlanc M, Staff AC, Söderhäll C, Vettukattil R, Ådalen S, Aaneland H, Lødrup Carlsen KC, Skjerven HO, Nordlund B (2022)
Evaluation of Skin Prick Test Reading Time at 10 versus 15 min in Young Infants
Int Arch Allergy Immunol, 183 (8), 824-834
DOI 10.1159/000522526, PubMed 35350034

Hilde K, Lødrup Carlsen KC, Bains KES, Gudmundsdóttir HK, Jonassen CM, Kreyberg I, LeBlanc M, Nordhagen L, Nordlund B, Rehbinder EM, Sjøborg KD, Skjerven HO, Staff AC, Sundet BK, Vettukattil R, Vaernesbranden MR, Wiik J, Haugen G (2021)
Fetal Thoracic Circumference and Lung Volume and Their Relation to Fetal Size and Pulmonary Artery Blood Flow
J Ultrasound Med, 41 (4), 985-993
DOI 10.1002/jum.15785, PubMed 34289520

Endre KMA, Landrø L, LeBlanc M, Gjersvik P, Carlsen KL, Haugen G, Hedlin G, Jonassen CM, Nordlund B, Rudi K, Skjerven HO, Staff AC, Söderhäll C, Vettukattil R, Rehbinder EM (2021)
Eczema distribution in girls and boys during infancy: A cohort study on atopic dermatitis
J Allergy Clin Immunol Pract, 9 (9), 3513-3516.e2
DOI 10.1016/j.jaip.2021.04.053, PubMed 33964509

Jarvis KB, Nielsen RL, Gupta R, Hede FD, Huttunen P, Jónsson ÓG, Rank CU, Ranta S, Saks K, Trakymiene SS, Tuckuviene R, Tulstrup M, INVENT consortium, Ruud E, Schmiegelow K, LeBlanc M (2020)
Polygenic risk score-analysis of thromboembolism in patients with acute lymphoblastic leukemia
Thromb Res, 196, 15-20
DOI 10.1016/j.thromres.2020.08.015, PubMed 32818716

Olstad OK, Gautvik VT, LeBlanc M, Kvernevik KJ, Utheim TP, Runningen A, Wiig H, Kirkegaard C, Raastad T, Reppe S, Gautvik KM (2020)
Postmenopausal osteoporosis is a musculoskeletal disease with a common genetic trait which responds to strength training: a translational intervention study
Ther Adv Musculoskelet Dis, 12, 1759720X20929443
DOI 10.1177/1759720X20929443, PubMed 32536985

Skjerven HO, Rehbinder EM, Vettukattil R, LeBlanc M, Granum B, Haugen G, Hedlin G, Landrø L, Marsland BJ, Rudi K, Sjøborg KD, Söderhäll C, Staff AC, Carlsen KH, Asarnoj A, Bains KES, Carlsen OCL, Endre KMA, Granlund PA, Hermansen JU, Gudmundsdóttir HK, Hilde K, Håland G, Kreyberg I, Olsen IC et al. (2020)
Skin emollient and early complementary feeding to prevent infant atopic dermatitis (PreventADALL): a factorial, multicentre, cluster-randomised trial
Lancet, 395 (10228), 951-961
DOI 10.1016/S0140-6736(19)32983-6, PubMed 32087121

Jarvis KB, LeBlanc M, Tulstrup M, Nielsen RL, Albertsen BK, Gupta R, Huttunen P, Jónsson ÓG, Rank CU, Ranta S, Ruud E, Saks K, Trakymiene SS, Tuckuviene R, Schmiegelow K (2019)
Candidate single nucleotide polymorphisms and thromboembolism in acute lymphoblastic leukemia - A NOPHO ALL2008 study
Thromb Res, 184, 92-98
DOI 10.1016/j.thromres.2019.11.002, PubMed 31715544

Wikenius E, Myhre AM, Page CM, Moe V, Smith L, Heiervang ER, Undlien DE, LeBlanc M (2019)
Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study
Nord J Psychiatry, 73 (4-5), 257-263
DOI 10.1080/08039488.2019.1613446, PubMed 31070508

Moen GH, LeBlanc M, Sommer C, Prasad RB, Lekva T, Normann KR, Qvigstad E, Groop L, Birkeland KI, Evans DM, Frøslie KF (2018)
Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort
Eur J Endocrinol, 179 (6), 363-372
DOI 10.1530/EJE-18-0478, PubMed 30324795

Nustad HE, Almeida M, Canty AJ, LeBlanc M, Page CM, Melton PE (2018)
Epigenetics, heritability and longitudinal analysis
BMC Genet, 19 (Suppl 1), 77
DOI 10.1186/s12863-018-0648-1, PubMed 30255778

Nustad HE, Page CM, Reiner AH, Zucknick M, LeBlanc M (2018)
A Bayesian mixed modeling approach for estimating heritability
BMC Proc, 12 (Suppl 9), 31
DOI 10.1186/s12919-018-0131-z, PubMed 30275883

LeBlanc M, Nustad HE, Zucknick M, Page CM (2018)
Quality control for Illumina 450K methylation data in the absence of iDat files using correlation structure in pedigrees and repeated measures
BMC Genet, 19 (Suppl 1), 66
DOI 10.1186/s12863-018-0636-5, PubMed 30255766

LeBlanc M, Zuber V, Thompson WK, Andreassen OA, Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium, Frigessi A, Andreassen BK (2018)
A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework
BMC Genomics, 19 (1), 494
DOI 10.1186/s12864-018-4859-7, PubMed 29940862

Halvorsen AR, Bjaanæs M, LeBlanc M, Holm AM, Bolstad N, Rubio L, Peñalver JC, Cervera J, Mojarrieta JC, López-Guerrero JA, Brustugun OT, Helland Å (2016)
A unique set of 6 circulating microRNAs for early detection of non-small cell lung cancer
Oncotarget, 7 (24), 37250-37259
DOI 10.18632/oncotarget.9363, PubMed 27191990

Moritz V, Holme O, Leblanc M, Hoff G (2016)
An explorative study from the Norwegian Quality Register Gastronet comparing self-estimated versus registered quality in colonoscopy performance
Endosc Int Open, 4 (3), E326-32
DOI 10.1055/s-0042-100904, PubMed 27004252

Reppe S, Wang Y, Thompson WK, McEvoy LK, Schork AJ, Zuber V, LeBlanc M, Bettella F, Mills IG, Desikan RS, Djurovic S, Gautvik KM, Dale AM, Andreassen OA, GEFOS Consortium (2015)
Genetic Sharing with Cardiovascular Disease Risk Factors and Diabetes Reveals Novel Bone Mineral Density Loci
PLoS One, 10 (12), e0144531
DOI 10.1371/journal.pone.0144531, PubMed 26695485

LeBlanc M, Zuber V, Andreassen BK, Witoelar A, Zeng L, Bettella F, Wang Y, McEvoy LK, Thompson WK, Schork AJ, Reppe S, Barrett-Connor E, Ligthart S, Dehghan A, Gautvik KM, Nelson CP, Schunkert H, Samani NJ, CARDIoGRAM Consortium, Ridker PM, Chasman DI, Aukrust P, Djurovic S, Frigessi A, Desikan RS et al. (2015)
Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors
Circ Res, 118 (1), 83-94
DOI 10.1161/CIRCRESAHA.115.306629, PubMed 26487741

LeBlanc M, Kulle B, Sundet K, Agartz I, Melle I, Djurovic S, Frigessi A, Andreassen OA (2011)
Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function
J Psychiatr Res, 46 (2), 271-8
DOI 10.1016/j.jpsychires.2011.11.001, PubMed 22126837

Guernsey DL, Matsuoka M, Jiang H, Evans S, Macgillivray C, Nightingale M, Perry S, Ferguson M, LeBlanc M, Paquette J, Patry L, Rideout AL, Thomas A, Orr A, McMaster CR, Michaud JL, Deal C, Langlois S, Superneau DW, Parkash S, Ludman M, Skidmore DL, Samuels ME (2011)
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
Nat Genet, 43 (4), 360-4
DOI 10.1038/ng.777, PubMed 21358631