Jessika Nordin
Bioinformatiker vid Institutionen för immunologi, genetik och patologi; Faciliteter; Klinisk genomik Uppsala
- E-post:
- jessika.nordin@igp.uu.se
- Besöksadress:
- Dag Hammarskjölds väg 20
751 85 Uppsala - Postadress:
- Rudbecklaboratoriet
751 85 UPPSALA

Publikationer
Senaste publikationer
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Ingår i Clinical Cancer Research, s. 3062-3071, 2025
- DOI för Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study
- Ladda ner fulltext (pdf) av Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study
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Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
Ingår i Proceedings of the National Academy of Sciences of the United States of America, 2023
- DOI för Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
- Ladda ner fulltext (pdf) av Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
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Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Ingår i Science, s. 367-+, 2023
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Ingår i Rheumatology, s. 3461-3470, 2022
- DOI för Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
- Ladda ner fulltext (pdf) av Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
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Ingår i Scandinavian Journal of Rheumatology, s. 21-24, 2022
- DOI för Allele frequency spectrum of known ankylosing spondylitis associated variants in a Swedish population
- Ladda ner fulltext (pdf) av Allele frequency spectrum of known ankylosing spondylitis associated variants in a Swedish population
Alla publikationer
Artiklar i tidskrift
-
Ingår i Clinical Cancer Research, s. 3062-3071, 2025
- DOI för Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study
- Ladda ner fulltext (pdf) av Validation of Guidelines for Genetic Investigation of Myeloid Neoplasms with Germline Predisposition: Results from a Prospective Cohort Study
-
Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
Ingår i Proceedings of the National Academy of Sciences of the United States of America, 2023
- DOI för Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
- Ladda ner fulltext (pdf) av Using evolutionary constraint to define novel candidate driver genes in medulloblastoma
-
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Ingår i Science, s. 367-+, 2023
-
Ingår i Rheumatology, s. 3461-3470, 2022
- DOI för Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
- Ladda ner fulltext (pdf) av Identification and Functional Characterization of a Novel Susceptibility Locus for Small Vessel Vasculitis with MPO-ANCA
-
Ingår i Scandinavian Journal of Rheumatology, s. 21-24, 2022
- DOI för Allele frequency spectrum of known ankylosing spondylitis associated variants in a Swedish population
- Ladda ner fulltext (pdf) av Allele frequency spectrum of known ankylosing spondylitis associated variants in a Swedish population
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Association of Protective HLA-A With HLA-B∗27 Positive Ankylosing Spondylitis
Ingår i Frontiers in Genetics, 2021
- DOI för Association of Protective HLA-A With HLA-B∗27 Positive Ankylosing Spondylitis
- Ladda ner fulltext (pdf) av Association of Protective HLA-A With HLA-B∗27 Positive Ankylosing Spondylitis
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A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
Ingår i Communications Biology, 2021
- DOI för A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
- Ladda ner fulltext (pdf) av A novel canine reference genome resolves genomic architecture and uncovers transcript complexity
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SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes
Ingår i European Journal of Human Genetics, s. 627-635, 2020
- DOI för SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes
- Ladda ner fulltext (pdf) av SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes
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Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
Ingår i Scientific Reports, 2020
- DOI för Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
- Ladda ner fulltext (pdf) av Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
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Ingår i Scientific Reports, 2018
- DOI för Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
- Ladda ner fulltext (pdf) av Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden
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Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
Ingår i Journal of Internal Medicine, s. 595-608, 2016
- DOI för Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease
- Ladda ner fulltext (pdf) av Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease