| The nature of nurture: Effects of parental genotypes A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ... Science 359 (6374), 424-428, 2018 | 859 | 2018 |
| Genetic insights into biological mechanisms governing human ovarian ageing KS Ruth, FR Day, J Hussain, A Martínez-Marchal, CE Aiken, A Azad, ... Nature 596 (7872), 393-397, 2021 | 263 | 2021 |
| Deconstructing the sources of genotype-phenotype associations in humans AI Young, S Benonisdottir, M Przeworski, A Kong Science 365 (6460), 1396-1400, 2019 | 258 | 2019 |
| Mendelian imputation of parental genotypes improves estimates of direct genetic effects AI Young, SM Nehzati, S Benonisdottir, A Okbay, H Jayashankar, C Lee, ... Nature genetics 54 (6), 897-905, 2022 | 120 | 2022 |
| A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ... Nature genetics 51 (2), 267-276, 2019 | 113 | 2019 |
| Obesity and risk of female reproductive conditions: A Mendelian randomisation study SS Venkatesh, T Ferreira, S Benonisdottir, N Rahmioglu, CM Becker, ... PLoS medicine 19 (2), e1003679, 2022 | 104 | 2022 |
| A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease GA Arnadottir, GL Norddahl, S Gudmundsdottir, AB Agustsdottir, ... Nature Communications 9 (1), 4447, 2018 | 104 | 2018 |
| Genome-wide association meta-analysis yields 20 loci associated with gallstone disease E Ferkingstad, A Oddsson, S Gretarsdottir, S Benonisdottir, G Thorleifsson, ... Nature communications 9 (1), 5101, 2018 | 95 | 2018 |
| Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase RP Kristjansson, A Oddsson, H Helgason, G Sveinbjornsson, ... Nature communications 7 (1), 10572, 2016 | 89 | 2016 |
| GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures U Styrkarsdottir, OA Stefansson, K Gunnarsdottir, G Thorleifsson, SH Lund, ... Nature communications 10 (1), 2054, 2019 | 85 | 2019 |
| A Missense Variant in PLEC Increases Risk of Atrial Fibrillation RB Thorolfsdottir, G Sveinbjornsson, P Sulem, A Helgadottir, ... Journal of the American College of Cardiology 70 (17), 2157-2168, 2017 | 82 | 2017 |
| Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis TA Olafsdottir, F Theodors, K Bjarnadottir, US Bjornsdottir, AB Agustsdottir, ... Nature Communications 11 (1), 393, 2020 | 81 | 2020 |
| Epigenetic and genetic components of height regulation S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ... Nature communications 7 (1), 13490, 2016 | 68 | 2016 |
| COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA BO Jensson, S Hansdottir, GA Arnadottir, G Sulem, RP Kristjansson, ... BMC medical genetics 18, 1-5, 2017 | 53 | 2017 |
| Genetic insight into sick sinus syndrome RB Thorolfsdottir, G Sveinbjornsson, HM Aegisdottir, S Benonisdottir, ... European heart journal 42 (20), 1959-1971, 2021 | 48 | 2021 |
| Sequence variant at 8q24. 21 associates with sciatica caused by lumbar disc herniation G Bjornsdottir, S Benonisdottir, G Sveinbjornsson, U Styrkarsdottir, ... Nature communications 8 (1), 14265, 2017 | 44 | 2017 |
| Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis GR Oskarsson, A Oddsson, MK Magnusson, RP Kristjansson, ... Communications biology 3 (1), 189, 2020 | 36 | 2020 |
| The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis EV Ivarsdottir, H Holm, S Benonisdottir, T Olafsdottir, G Sveinbjornsson, ... Communications Biology 4 (1), 706, 2021 | 34 | 2021 |
| Sequence variants associating with urinary biomarkers S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ... Human Molecular Genetics 28 (7), 1199-1211, 2019 | 32 | 2019 |
| Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters GA Arnadottir, BO Jensson, SE Marelsson, G Sulem, A Oddsson, ... BMC medical genetics 18, 1-5, 2017 | 32 | 2017 |
