Publications

Identifying multimodal signatures underlying the somatic comorbidity of psychosis: the COMMITMENT roadmap.

Schwarz E, Alnæs D, Andreassen OA, Cao H, Chen J, Degenhardt F, Doncevic D, Dwyer D, Eils R, Erdmann J, Herrmann C, Hofmann-Apitius M, Kaufmann T, Koutsouleris N, Kodamullil AT, Khuntia A, Mucha S, Nöthen MM, Paul R, Pedersen ML, Quintero A, Schunkert H, Sharma A, Tost H, Westlye LT, Zhang Y, Meyer-Lindenberg A.

Mol Psychiatry. 2020 Oct 15. doi: 10.1038/s41380-020-00915-z.

https://pubmed.ncbi.nlm.nih.gov/33060817/

The Macrophage Migration Inhibitory Factor (MIF) promoter polymorphisms (rs3063368, rs755622) predict acute kidney injury and death after cardiac surgery

Averdunk L, Bernhagen J, Fehnle K, Surowy H, Lüdecke HJ, Mucha S, Meybohm P, Wieczorek D, Leng L, Marx G, Leaf DE, Zarbock A, Zacharowski K, On Behalf Of The RIPHeart Study Collaborators, Bucala R, Stoppe C.

J Clin Med. 2020 Sep 11;9(9):E2936. doi: 10.3390/jcm9092936.

https://pubmed.ncbi.nlm.nih.gov/32932965/

Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

Nomura A, Emdin CA, Won HH, Peloso GM, Natarajan P, Ardissino D, Danesh J, Schunkert H, Correa A, Bown MJ, Samani NJ, Erdmann J, McPherson R, Watkins H, Saleheen D, Elosua R, Kawashiri MA, Tada H, Gupta N, Shah SH, Rader DJ, Gabriel S, Khera AV, Kathiresan S.

Circ Genom Precis Med. 2020 Aug 30. doi: 10.1161/CIRCGEN.119.002871.

https://pubmed.ncbi.nlm.nih.gov/32862661/

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan.

Rasool S, Baig JM, Moawia A, Ahmad I, Iqbal M, Waseem SS, Asif M, Abdullah U, Makhdoom EUH, Kaygusuz E, Zakaria M, Ramzan S, Haque SU, Mir A, Anjum I, Fiaz M, Ali Z, Tariq M, Saba N, Hussain W, Budde B, Irshad S, Noegel AA, Höning S, Baig SM, Nürnberg P, Hussain MS.

Mol Genet Genomic Med. 2020 Jul 17:e1408. doi: 10.1002/mgg3.1408.

https://pubmed.ncbi.nlm.nih.gov/32677750/

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