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Publications

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

Teumer A. et al, (2019), Nat Commun, 10

The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia.

Muriuki JM. et al, (2019), Science advances, 5

ToxNav germline genetic testing and PROMinet digital mobile application toxicity monitoring: Results of a prospective single-center clinical utility study-PRECISE study.

Lee LYW. et al, (2019), Cancer Med

Interferon lambda 4 impacts the genetic diversity of hepatitis C virus

Ansari MA. et al, (2019), eLife, 8

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.

Liu X. et al, (2019), Nat Commun, 10

The structural basis of lipid scrambling and inactivation in the endoplasmic reticulum scramblase TMEM16K.

Bushell SR. et al, (2019), Nat Commun, 10

A method for genome-wide genealogy estimation for thousands of samples.

Speidel L. et al, (2019), Nat Genet, 51, 1321 - 1329

Determinants of dihydroartemisinin-piperaquine treatment failure in Plasmodium falciparum malaria in Cambodia, Thailand, and Vietnam: a prospective clinical, pharmacological, and genetic study

van der Pluijm RW. et al, (2019), The Lancet Infectious Diseases, 19, 952 - 961

A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination.

Li R. et al, (2019), Nat Commun, 10

Atomic structure of the Epstein-Barr virus portal.

Machón C. et al, (2019), Nat Commun, 10

iASPP mediates p53 selectivity through a modular mechanism fine-tuning DNA recognition.

Chen S. et al, (2019), Proc Natl Acad Sci U S A, 116, 17470 - 17479

Frequent retrotransposition of endogenous genes in ERCC2-deficient cells derived from a patient with xeroderma pigmentosum.

Aoto S. et al, (2019), Stem Cell Res Ther, 10

Mechanisms of atrial fibrillation.

Wijesurendra RS. and Casadei B., (2019), Heart

Major subpopulations of Plasmodium falciparum in sub-Saharan Africa.

Amambua-Ngwa A. et al, (2019), Science, 365, 813 - 816

A method for non-invasive prenatal diagnosis of monogenic autosomal recessive disorders.

Cutts A. et al, (2019), Blood

Diversity of oligomerization in Drosophila semaphorins suggests a mechanism of functional fine-tuning.

Rozbesky D. et al, (2019), Nat Commun, 10

Genetic Predisposition to Type 2 Diabetes and Risk of Subclinical Atherosclerosis and Cardiovascular Diseases Among 160,000 Chinese adults

Gan W. et al, (2019), Diabetes, db190224 - db190224

Publisher Correction: The metabolite BH4 controls T cell proliferation in autoimmunity and cancer.

Cronin SJF. et al, (2019), Nature, 572

Correction: The Relative Contribution of Metabolic and Structural Abnormalities to Diastolic Dysfunction in Obesity.

Rayner JJ. et al, (2019), Int J Obes (Lond), 43

Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice.

Pagnamenta AT. et al, (2019), Hum Mol Genet

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