Author

Gerald Sulem

Observed names: G. Sulem, SULEM, Gérald, Sulem Gerald, Sulem, Gerald

Institution: deCODE Genetics (Iceland)

Observed institution: deCODE Genetics (Iceland)

OpenAlex ID: A5006280644

A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis

2019 · Ragnar P. Kristjansson, Stefania Benonisdottir, et al. · Nature Genetics · 123

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

2018 · Gudny A. Arnadottir, Gudmundur L. Norddahl, et al. · Nature Communications · 111

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

2017 · Unnur Styrkarsdottir, Hannes Helgason, et al. · Nature Genetics · 101

Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

2016 · Ragnar P. Kristjansson, Asmundur Oddsson, et al. · Nature Communications · 89

COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Brynjar O. Jensson, Sif Hansdottir, et al. · BMC Medical Genetics · 61

Epigenetic and genetic components of height regulation

2016 · Stefania Benonisdottir, Asmundur Oddsson, et al. · Nature Communications · 58

Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters

2017 · Gudny A. Arnadottir, Brynjar O. Jensson, et al. · BMC Medical Genetics · 48

Sequence variants associating with urinary biomarkers

2018 · Stefania Benonisdottir, Ragnar P Kristjansson, et al. · Human Molecular Genetics · 40

Correction: Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

2017 · Unnur Styrkarsdottir, Hannes Helgason, et al. · Nature Genetics · 2

Whole genome sequencing finds rare high-risk genotypes for hip osteoarthritis in the COMP and CHADL genes

2017 · T. Ingvarsson, U. Styrkarsdottir, et al. · Osteoarthritis and Cartilage · 1

Copaにおける再発性ミスセンス変異により引き起こされたアイスランド家族におけるcopa症候群【jst・京大機械翻訳】

2017 · O Jensson Brynjar, Hansdottir Sif, et al.

2姉妹における早期発症てんかん性脳症を引き起こすuba5における複合ヘテロ接合変異【jst・京大機械翻訳】

2017 · A Arnadottir Gudny, O Jensson Brynjar, et al.

Additional file 7: Figure S4. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 5: Table S2. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 2: Table S1. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 9: Table S4. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 3: Figure S2. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 1: Figure S1. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 10: Table S5. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 6: Supplementary Information. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 4: Figure S3. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Additional file 8: Table S3. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

2017 · Jensson, Brynjar, Hansdottir, Sif, et al. · Figshare

Works count: 34

Citation count: 634

H-index: 8

I10-index: 8