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Stem Cell Research|August 11, 2019
Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutationsJens Schuster, Ambrin Fatima, Maria Sobol, et al.
FEBS Letters|May 21, 2009
Posttranscriptional down-regulation of small ribosomal subunit proteins correlates with reduction of 18S rRNA in RPS19 deficiencyJitendra Badhai, Anne-Sophie Fröjmark, Hamid Reza Razzaghian, et al.
Elife|August 27, 2024
Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implicationsJens Schuster, Xi Lu, Yonglong Dang, et al.
RNA (New York, N.Y.)|July 11, 2006
U1-like snRNAs lacking complementarity to canonical 5' splice sitesChristina Kyriakopoulou, Pontus Larsson, Lei Liu, et al.
Stem Cell Research|March 4, 2020
Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9Ambrin Fatima, Jens Schuster, Talia Akram, et al.
Frontiers in Immunology|June 16, 2025
Comprehensive transcriptome assessment in PBMCs of post-COVID patients at a median follow-up of 28 months after a mild COVID infection reveals upregulation of JAK/STAT signaling and a prolonged immune responseSerena Fineschi, Joakim Klar, Juan Ramon Lopez Egido, et al.
BMC Medical Genetics|June 26, 2014
Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophyJens Schuster, Tahir Naeem Khan, Muhammad Tariq, et al.
Nature Communications|July 14, 2016
Human serum-derived protein removes the need for coating in defined human pluripotent stem cell cultureSara Pijuan-Galitó, Christoffer Tamm, Jens Schuster, et al.
Plos One|July 10, 2009
Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS19Alvaro Martinez Barrio, Oskar Eriksson, Jitendra Badhai, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndromeSadia Nawaz, Joakim Klar, Muhammad Wajid, et al.
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