Recurrent events and the exploding Cox model

by Gjessing, Håkon K., Røysland, Kjetil, Pena, Edsel A., Aalen, Odd O.
Published 2010

Seed viability and germination success of Acacia tortilis along land‐use and aridity gradients in the Eastern Sahara

by Andersen, Gidske Leknæs, Krzywinski, Knut, Gjessing, Håkon K., Pierce, Richard Holton
Published in Ecol Evol (2015)

Maternal angiotensinogen (AGT) haplotypes, fetal renin (REN) haplotypes and risk of preeclampsia; estimation of gene-gene interaction from family-triad data

by Vefring, Hege K, Wee, Line, Jugessur, Astanand, Gjessing, Håkon K, Nilsen, Stein T, Lie, Rolv T
Published 2010

Parent‐of‐origin‐environment interactions in case‐parent triads with or without independent controls

by Gjerdevik, Miriam, Haaland, Øystein A., Romanowska, Julia, Lie, Rolv T., Jugessur, Astanand, Gjessing, Håkon K.
Published in Ann Hum Genet (2017)

A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use a...

by Haaland, Øystein A., Lie, Rolv T., Romanowska, Julia, Gjerdevik, Miriam, Gjessing, Håkon K., Jugessur, Astanand
Published in Front Genet (2018)

A fast wavelet-based functional association analysis replicates several susceptibility loci for birth weight in a Norwegian population

by Denault, William R. P., Romanowska, Julia, Helgeland, Øyvind, Jacobsson, Bo, Gjessing, Håkon K., Jugessur, Astanand
Published in BMC Genomics (2021)

Fetal and maternal contributions to risk of pre-eclampsia: population based study

by Lie, Rolv Terje, Rasmussen, Svein, Brunborg, Helge, Gjessing, Håkon K, Lie-Nielsen, Erik, Irgens, Lorentz M
Published 1998

A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts

by Skare, Øivind, Gjessing, Håkon K., Gjerdevik, Miriam, Haaland, Øystein A., Romanowska, Julia, Lie, Rolv T., Jugessur, Astanand
Published in PLoS One (2017)

Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2

by Skare, Øivind, Lie, Rolv T., Haaland, Øystein A., Gjerdevik, Miriam, Romanowska, Julia, Gjessing, Håkon K., Jugessur, Astanand
Published in Front Genet (2018)

Maternal smoking and oral clefts: The role of detoxification pathway genes

by Lie, Rolv T., Wilcox, Allen J, Taylor, Jack, Gjessing, Håkon K., Saugstad, Ola Didrik, Aabyholm, Frank, Vindenes, Halvard
Published in Epidemiology (2008)

Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes

by Clark, Michelle M., Chazara, Olympe, Sobel, Eric M., Gjessing, Håkon K., Magnus, Per, Moffett, Ashley, Sinsheimer, Janet S.
Published in Hum Hered (2017)

Haplin power analysis: a software module for power and sample size calculations in genetic association analyses of family triads and unrelated controls

by Gjerdevik, Miriam, Jugessur, Astanand, Haaland, Øystein A., Romanowska, Julia, Lie, Rolv T., Cordell, Heather J., Gjessing, Håkon K.
Published in BMC Bioinformatics (2019)

Risk Factors for Extended Duration of Acute Diarrhea in Young Children

by Strand, Tor A., Sharma, Pushpa R., Gjessing, Håkon K., Ulak, Manjeswori, Chandyo, Ram K., Adhikari, Ramesh K., Sommerfelt, Halvor
Published 2012

Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data

by Jugessur, Astanand, Wilcox, Allen J., Murray, Jeffrey C., Gjessing, Håkon K., Nguyen, Truc Trung, Nilsen, Roy M., Lie, Rolv T.
Published in Nor Epidemiol (2012)

Genetic Variants in IRF6 and the Risk of Facial Clefts: Single-Marker and Haplotype-Based Analyses in a Population-Based Case-Control Study of Facial Clefts in Norway

by Jugessur, Astanand, Rahimov, Fedik, Lie, Rolv T., Wilcox, Allen J., Gjessing, Håkon K., Nilsen, Roy M., Nguyen, Truc Trung, Murray, Jeffrey C.
Published 2008

Candidate gene analysis of spontaneous preterm delivery: New insights from re-analysis of a case-control study using case-parent triads and control-mother dyads

by Myking, Solveig, Myhre, Ronny, Gjessing, Håkon K, Morken, Nils-Halvdan, Sengpiel, Verena, Williams, Scott M, Ryckman, Kelli K, Magnus, Per, Jacobsson, Bo
Published 2011

X-Linked Genes and Risk of Orofacial Clefts: Evidence from Two Population-Based Studies in Scandinavia

by Jugessur, Astanand, Skare, Øivind, Lie, Rolv T., Wilcox, Allen J., Christensen, Kaare, Christiansen, Lene, Nguyen, Truc Trung, Murray, Jeffrey C., Gjessing, Håkon K.
Published 2012

Gene–methylation interactions: discovering region-wise DNA methylation levels that modify SNP-associated disease risk

by Romanowska, Julia, Haaland, Øystein A., Jugessur, Astanand, Gjerdevik, Miriam, Xu, Zongli, Taylor, Jack, Wilcox, Allen J., Jonassen, Inge, Lie, Rolv T., Gjessing, Håkon K.
Published in Clin Epigenetics (2020)

Growth in children conceived by ART

by Magnus, Maria C, Wilcox, Allen J, Fadum, Elin A, Gjessing, Håkon K, Opdahl, Signe, Juliusson, Petur B, Romundstad, Liv Bente, Håberg, Siri E
Published in Hum Reprod (2021)

Wavelet Screening identifies regions highly enriched for differentially methylated loci for orofacial clefts

by Denault, William R P, Romanowska, Julia, Haaland, Øystein A, Lyle, Robert, Taylor, Jack A, Xu, Zongli, Lie, Rolv T, Gjessing, Håkon K, Jugessur, Astanand
Published in NAR Genom Bioinform (2021)