Genome Med

ISSN	1756-994X
ISSN-L	1756-994X
IUID	8739bb081ff443258539f5d55ffbe740
Modified	2020-11-27T13:12:56.945Z
Created	2018-12-05T09:43:15.096Z

Year 2025

PubMed DOI Crossref

varCADD: large sets of standing genetic variation enable genome-wide pathogenicity prediction.

Nazaretyan L, Rentzsch P, Kircher M

Genome Med 17 (1) 84 [2025-08-04; online 2025-08-04]

PubMed DOI Crossref

The dynamics of the gut microbiota in prediabetes during a four-year follow-up among European patients-an IMI-DIRECT prospective study.

Lyu L, Fan Y, Vogt JK, ..., Pearson E, Pedersen O

Genome Med 17 (1) 78 [2025-07-15; online 2025-07-15]

PubMed DOI Crossref

Longitudinal analysis of genetic and environmental interplay in human metabolic profiles and the implication for metabolic health.

Wang J, Zenere A, Wang X, ..., Uhlén M, Zhong W

Genome Med 17 (1) 68 [2025-06-17; online 2025-06-17]

DDLS Fellow Fredrik Edfors

Year 2023

PubMed DOI Crossref

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Matuozzo D, Talouarn E, Marchal A, ..., Abel L, Cobat A

Genome Med 15 (1) 22 [2023-04-05; online 2023-04-05]

Year 2022

PubMed DOI Crossref

Loss of Y in leukocytes as a risk factor for critical COVID-19 in men.

Bruhn-Olszewska B, Davies H, Sarkisyan D, ..., Frithiof R, Dumanski JP

Genome Med 14 (1) 139 [2022-12-14; online 2022-12-14]

PubMed DOI Crossref

Integrative genomic and transcriptomic analyses illuminate the ontology of HER2-low breast carcinomas.

Berrino E, Annaratone L, Bellomo SE, ..., Sapino A, Marchiò C

Genome Med 14 (1) 98 [2022-08-29; online 2022-08-29]

Year 2021

PubMed DOI Crossref

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients.

Stranneheim H, Lagerstedt-Robinson K, Magnusson M, ..., Lindstrand A, Wedell A

Genome Med 13 (1) 40 [2021-03-17; online 2021-03-17]

Year 2020

PubMed DOI Crossref

Whole blood co-expression modules associate with metabolic traits and type 2 diabetes: an IMI-DIRECT study.

Gudmundsdottir V, Pedersen HK, Mazzoni G, ..., Pedersen O, Brunak S

Genome Med 12 (1) 109 [2020-12-01; online 2020-12-01]

PubMed DOI Crossref

Whole-genome sequence association analysis of blood proteins in a longitudinal wellness cohort.

Zhong W, Gummesson A, Tebani A, ..., Fagerberg L, Uhlén M

Genome Med 12 (1) 53 [2020-06-23; online 2020-06-23]

DDLS Fellow Fredrik Edfors

PubMed DOI Crossref

Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age.

Merid SK, Novoloaca A, Sharp GC, ..., London SJ, Melén E

Genome Med 12 (1) 25 [2020-03-02; online 2020-03-02]

PubMed DOI Crossref

Towards a European health research and innovation cloud (HRIC).

Aarestrup FM, Albeyatti A, Armitage WJ, ..., Van den Bulcke M, Van Oyen H

Genome Med 12 (1) 18 [2020-02-19; online 2020-02-19]

Year 2019

PubMed DOI Crossref

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.

Lindstrand A, Eisfeldt J, Pettersson M, ..., Lundin J, Nilsson D

Genome Med 11 (1) 68 [2019-11-07; online 2019-11-07]

PubMed DOI Crossref

A validated single-cell-based strategy to identify diagnostic and therapeutic targets in complex diseases.

Gawel DR, Serra-Musach J, Lilja S, ..., Gustafsson M, Benson M

Genome Med 11 (1) 47 [2019-07-30; online 2019-07-30]

Antonio Lentini DDLS Fellow

Year 2018

PubMed DOI Crossref

Cell-free DNA profiling of metastatic prostate cancer reveals microsatellite instability, structural rearrangements and clonal hematopoiesis.

Mayrhofer M, De Laere B, Whitington T, ..., Grönberg H, Lindberg J

Genome Med 10 (1) 85 [2018-11-21; online 2018-11-21]

PubMed DOI Crossref

Linking FOXO3, NCOA3, and TCF7L2 to Ras pathway phenotypes through a genome-wide forward genetic screen in human colorectal cancer cells.

Kundu S, Ali MA, Handin N, ..., Hellström M, Sjöblom T

Genome Med 10 (1) 2 [2018-01-04; online 2018-01-04]

Year 2017

PubMed DOI Crossref

Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans.

Gottlieb A, Daneshjou R, DeGorter M, ..., Montgomery SB, Altman RB

Genome Med 9 (1) 98 [2017-11-24; online 2017-11-24]

PubMed DOI Crossref

Type 2 diabetes and obesity induce similar transcriptional reprogramming in human myocytes.

Väremo L, Henriksen TI, Scheele C, ..., Pedersen BK, Nielsen J

Genome Med 9 (1) 47 [2017-05-25; online 2017-05-25]

Year 2014

PubMed DOI Crossref

Fourth-generation sequencing in the cell and the clinic.

Mignardi M, Nilsson M

Genome Med 6 (4) 31 [2014-04-28; online 2014-04-28]

Year 2012

PubMed DOI Crossref

Comprehensive analysis of the genome transcriptome and proteome landscapes of three tumor cell lines.

Akan P, Alexeyenko A, Costea PI, ..., Uhlén M, Lundeberg J

Genome Med 4 (11) 86 [2012-11-18; online 2012-11-18]