Eli and Edythe L. Broad Institute of MIT and Harvard

Research facility


Location: Cambridge, MA, United States (USA) (US) US

ISNI: 000000405461623

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Reconstructing cell cycle and disease progression using deep learning (2017) Eulenberg P, Koehler N, Blasi T, Filby A, Carpenter AE, Rees P, Theis FJ, Wolf FA Journal article AML1-ETO requires enhanced C/D box snoRNA/RNP formation to induce self-renewal and leukaemia. (2017) Zhou F, Liu Y, Rohde C, Pauli C, Gerloff D, Koehn M, Misiak D, et al. Journal article, Original article Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) Witt SH, Streit F, Jungkunz M, Frank J, Awasthi S, Reinbold CS, Treutlein J, et al. Journal article DISCOVERY AND PATHOGENICITY ASSESSMENT OF NEUROPATHOLOGY-ASSOCIATED GENE VARIANTS (2017) Neupert LM, May P, Kobow K, Nothnagel M, Nuernberg P, Freiman T, Harter P, et al. Conference contribution Type i interferons and microbial metabolites of tryptophan modulate astrocyte activity and central nervous system inflammation via the aryl hydrocarbon receptor (2016) Rothhammer V, Mascanfroni ID, Bunse L, Takenaka MC, Kenison JE, Mayo L, Chao CC, et al. Journal article Label-free cell cycle analysis for high-throughput imaging flow cytometry (2016) Blasi T, Hennig H, Summers HD, Theis FJ, Cerveira J, Patterson JO, Davies D, et al. Journal article Asymmetric dimethylarginine, related arginine derivatives, and incident atrial fibrillation (2016) Schnabel RB, Maas R, Wang N, Yin X, Larson MG, Levy D, Ellinor PT, et al. Journal article Inactivating mutations in NPC1L1 and protection from coronary heart disease (2014) Stitziel NO, Won HH, Morrison AC, Peloso GM, Do R, Lange LA, Fontanillas P, et al. Journal article CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration (2014) Schaffer AE, Eggens VRC, Caglayan AO, Reuter M, Scott E, Coufal NG, Silhavy JL, et al. Journal article
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