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Stanford Department of Genetics

Stanford Department of Genetics diagram by undefined

Find the latest research from the Stanford Medicine Department of Genetics here.

Top 20 most recent papers
Cell

Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa

CellOctober 31, 2019
Deepti GurdasaniManj S Sandhu
171
15
1
33
Nature

Circular ecDNA promotes accessible chromatin and high oncogene expression

NatureNovember 20, 2019
Sihan WuPaul S. Mischel
546
106
5
1
3
1
Blood

First-in-Human Assessment of Feasibility and Safety of Multiplexed Genetic Engineering of Autologous T Cells Expressing NY-ESO -1 TCR and CRISPR/Cas9 Gene Edited to Eliminate Endogenous TCR and PD-1 (NYCE T cells) in Advanced Multiple Myeloma (MM) and Sarcoma

BloodNovember 13, 2019
Edward A StadtmauerCarl H. June
3
Science

Ancient Rome: A genetic crossroads of Europe and the Mediterranean

ScienceNovember 8, 2019
Margaret L. L. AntonioJonathan K. Pritchard
1236
50
2
4
5
Nature Communications

GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

Nature CommunicationsOctober 31, 2019
Elena López-IsacJavier Martín
33
Nature Methods

Biological plasticity rescues target activity in CRISPR knock outs

Nature MethodsOctober 30, 2019
Arne H SmitsWolfgang W Huber
871
2
5
1
Nature Biotechnology

Author Correction: Efficient proximity labeling in living cells and organisms with TurboID

Nature BiotechnologyNovember 20, 2019
Tess Caroline BranonAlice Y. Ting
Nature Biotechnology

Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia

Nature BiotechnologyDecember 2, 2019
Jeffrey M. GranjaWilliam James Greenleaf
288
1
1
bioRxiv

Frequent extrachromosomal oncogene amplification drives aggressive tumors

bioRxivNovember 28, 2019
Hoon KimRoel G.W. Verhaak
82
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research

Association of Tumor Infiltrating Lymphocytes with Homologous Recombination Deficiency and BRCA1/2 Status in Patients with Early Triple-Negative Breast Cancer: A Pooled Analysis

Clinical Cancer Research : an Official Journal of the American Association for Cancer ResearchDecember 3, 2019
Melinda L TelliAndrea Lynn Richardson
bioRxiv

Structural modularity of the XIST ribonucleoprotein complex

bioRxivNovember 24, 2019
Zhipeng LuHoward Y. Chang
24
Genome Biology

Genetic regulation of gene expression and splicing during a 10-year period of human aging

Genome BiologyNovember 4, 2019
Brunilda BalliuStephen Blaire Montgomery
58
Nature

c-Jun overexpression in CAR T cells induces exhaustion resistance

NatureDecember 4, 2019
Rachel Christina LynnCrystal L. Mackall
137
3
4
bioRxiv

Deep functional synthesis: a machine learning approach to gene functional enrichment

bioRxivNovember 13, 2019
Sheng Fu WangTrey G Ideker
38
bioRxiv

Pan-cancer analysis of clonality and the timing of systemic spread in paired primary tumors and metastases

bioRxivOctober 31, 2019
Zheng HuChristina N Curtis
29
Nucleic Acids Research

New developments on the Encyclopedia of DNA Elements (ENCODE) data portal

Nucleic Acids ResearchNovember 12, 2019
Yunhai LuoJ. Michael Cherry
bioRxiv

A genome-wide almanac of co-essential modules assigns function to uncharacterized genes

bioRxivNovember 1, 2019
Michael WainbergMichael Cory Bassik
53
bioRxiv

Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx

bioRxivNovember 9, 2019
Nicole R GayStephen Blaire Montgomery
72
Nature Medicine

Chromatin regulators mediate anthracycline sensitivity in breast cancer

Nature MedicineNovember 7, 2019
José A SeoaneChristina N Curtis
122
3
4
Kidney International

Epidemiology, molecular, and genetic methodologies to evaluate causes of CKDu around the world: report of the Working Group from the ISN International Consortium of Collaborators on CKDu

Kidney InternationalNovember 25, 2019
Shuchi AnandInternational Society of Nephrology’s International Consortium of Collaborators on Chronic Kidney Disease of Unknown Etiology (i3C)
13
1

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