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1 . Academic Journal
Uncommon Variants in FLG2 and NOD2 Are Associated with Atopic Dermatitis in the Ethiopian Population
저자
by
Wang, Sailan
;
Elmgren, Julia K.
;
Eisfeldt, Jesper
;
Asad, Samina
;
Ek, Marlene
, et al.
소스
In
JID Innovations
July 2024 4(4)
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7 . Academic Journal
A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements
저자
by
Schuy, Jakob
;
Sæther, Kristine Bilgrav
;
Lisfeld, Jasmin
;
Ek, Marlene
;
Grochowski, Christopher M.
, et al.
소스
In
Genetics in Medicine Open
2024 2
Full Text (ScienceDirect)
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7 . Academic Journal
Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma
저자
by
Peña-Pérez, Lucía
;
Frengen, Nicolai
;
Hauenstein, Julia
;
Gran, Charlotte
;
Gustafsson, Charlotte
, et al.
소스
In
Blood Advances
13 September 2022 6(17):5009-5023
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7 . Academic Journal
A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins
저자
by
Bang, Benedicte
;
Eisfeldt, Jesper
;
Barbany, Gisela
;
Harila-Saari, Arja
;
Heyman, Mats
, et al.
소스
In
Blood Advances
12 April 2022 6(7):2275-2289
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7 . Conference
Ecosystem Models Based on Artificial Intelligence
저자
by
Strannegard, Claes
;
Engsner, Niklas
;
Eisfeldt, Jesper
;
Endler, John
;
Hansson, Amanda
, et al.
소스
2022 Swedish Artificial Intelligence Society Workshop (SAIS) Artificial Intelligence Society Workshop (SAIS), 2022 Swedish. :1-9 Jun, 2022
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7 . Academic Journal
Long-read sequencing and optical mapping generates near T2T assemblies that resolves a centromeric translocation.
저자
by
ten Berk de Boer, Esmee
;
Ameur, Adam
;
Bunikis, Ignas
;
Ek, Marlene
;
Stattin, Eva-Lena
, et al.
소스
Scientific Reports
. 4/18/2024, Vol. 14 Issue 1, p1-8. 8p.
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7 . Academic Journal
Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans.
저자
by
Wang, Sailan
;
Nikamo, Pernilla
;
Laasonen, Leena
;
Gudbjornsson, Bjorn
;
Ejstrup, Leif
, et al.
소스
EMBO Molecular Medicine; Mar2024, Vol. 16 Issue 3, p596-615, 20p
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7 . Academic Journal
Mosaic deletions of known genes explain skeletal dysplasias with high and low bone mass
저자
by
Muurinen, Mari
;
Taylan, Fulya
;
Tournis, Tournis
;
Eisfeldt, Jesper
;
Balanika, Alexia
, et al.
소스
In
Bone Reports
May 2022 16 Supplement
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7 . Academic Journal
Insights into cellular behavior and micromolecular communication in urothelial micrografts.
저자
by
Juul, Nikolai
;
Willacy, Oliver
;
Mamand, Doste R.
;
Andaloussi, Samir El
;
Eisfeldt, Jesper
, et al.
소스
Scientific Reports
. 11/18/2023, Vol. 13 Issue 1, p1-13. 13p.
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7 . Academic Journal
Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia.
저자
by
Rezayee, Fatemah
;
Eisfeldt, Jesper
;
Skaftason, Aron
;
Öfverholm, Ingegerd
;
Sayyab, Shumaila
, et al.
소스
Frontiers in Oncology; 2023, p01-14, 14p
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