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1 . Academic Journal
Reconstruction of the origin of the first major SARS-CoV-2 outbreak in Germany
저자
by
Korencak, Marek
;
Sivalingam, Sugirthan
;
Sahu, Anshupa
;
Dressen, Dietmar
;
Schmidt, Axel
, et al.
소스
In
Computational and Structural Biotechnology Journal
2022 20:2292-2296
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7 . Academic Journal
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections
저자
by
Kathiravel, Ushanthine
;
Keyser, Britta
;
Hoffjan, Sabine
;
Kötting, Judith
;
Müller, Melanie
, et al.
소스
In
Molecular and Cellular Probes
April 2013 27(2):103-108
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7 . Academic Journal
Gene-based burden scores identify rare variant associations for 28 blood biomarkers.
저자
by
Aldisi, Rana
;
Hassanin, Emadeldin
;
Sivalingam, Sugirthan
;
Buness, Andreas
;
Klinkhammer, Hannah
, et al.
소스
BMC Genomic Data
. 9/4/2023, Vol. 24 Issue 1, p1-11. 11p.
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7 . Academic Journal
T32. IMPACT OF BIPOLAR DISORDER POLYGENIC RISK ON GENE EXPRESSION IN IPSC-DERIVED NEURAL PROGENITORS FROM GENETICALLY CHARACTERIZED PATIENTS AND CONTROLS
저자
by
Hünten, Karola
;
Krutenko, Tamara
;
David, Friederike S.
;
Beins, Eva C.
;
Sivalingam, Sugirthan
, et al.
소스
In
European Neuropsychopharmacology
October 2023 75 Supplement 1:S178-S179
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7 . Academic Journal
W82. ANALYSING THE GENETIC BURDEN OF RARE AND POTENTIALLY DAMAGING VARIANTS IN SCHIZOPHRENIA RISK-LOCUS XQ28,DISTAL USING HIGH-THROUGHPUT, MULTIPLEX TARGETED SEQUENCING
저자
by
Claus, Isabelle
;
Sivalingam, Sugirthan
;
Hoffmann, Per
;
Streit, Fabian
;
Nenadić, Igor
, et al.
소스
In
European Neuropsychopharmacology
October 2023 75 Supplement 1:S147-S148
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7 . Academic Journal
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
저자
by
Ishorst, Nina
;
Henschel, Leonie
;
Thieme, Frederic
;
Drichel, Dmitriy
;
Sivalingam, Sugirthan
, et al.
소스
Molecular Genetics & Genomic Medicine
. Mar2023, Vol. 11 Issue 3, p1-16. 16p.
Open Access (Wiley)
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7 . Academic Journal
Altered Notch Signaling in Dowling-Degos Disease: Additional Mutations in POGLUT1 and Further Insights into Disease Pathogenesis
저자
by
Ralser, Damian J.
;
Takeuchi, Hideyuki
;
Fritz, Günter
;
Basmanav, F. Buket
;
Effern, Maike
, et al.
소스
In
Journal of Investigative Dermatology
April 2019 139(4):960-964
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7 . Academic Journal
Next‐generation phenotyping contributing to the identification of a 4.7 kb deletion in KANSL1 causing Koolen‐de Vries syndrome.
저자
by
Brand, Fabian
;
Vijayananth, Aswinkumar
;
Hsieh, Tzung‐Chien
;
Schmidt, Axel
;
Peters, Sophia
, et al.
소스
Human Mutation; Nov2022, Vol. 43 Issue 11, p1659-1665, 7p
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7 . Academic Journal
Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
저자
by
Henne, Sabrina Katrin
;
Aldisi, Rana
;
Sivalingam, Sugirthan
;
Hochfeld, Lara Maleen
;
Borisov, Oleg
, et al.
소스
Nature Communications
. 14(1)
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7 . Academic Journal
Heterogeneity and excitability of BRAFV600E-induced tumors is determined by Akt/mTOR-signaling state and Trp53-loss.
저자
by
Cases-Cunillera, Silvia
;
Loo, Karen M J van
;
Pitsch, Julika
;
Quatraccioni, Anne
;
Sivalingam, Sugirthan
, et al.
소스
Neuro-Oncology; May2022, Vol. 24 Issue 5, p741-754, 14p
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