Publisher Correction: Eggs sense high-fat diet.

Abstract:

:In the version of this article originally published, a box was misplaced in Fig. 1. The error has been corrected in the HTML and PDF versions of the article.

journal_name

Nat Genet

journal_title

Nature genetics

authors

Leitch HG,Hajkova P

doi

10.1038/s41588-018-0137-5

subject

Has Abstract

pub_date

2018-08-01 00:00:00

pages

1196

issue

8

eissn

1061-4036

issn

1546-1718

pii

10.1038/s41588-018-0137-5

journal_volume

50

pub_type

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    authors: Pál C,Hurst LD

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  • The Capsella rubella genome and the genomic consequences of rapid mating system evolution.

    abstract::The shift from outcrossing to selfing is common in flowering plants, but the genomic consequences and the speed at which they emerge remain poorly understood. An excellent model for understanding the evolution of self fertilization is provided by Capsella rubella, which became self compatible <200,000 years ago. We re...

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    abstract::Acquired mutations in the hematopoietic transcription factor GATA binding protein-1 (GATA1) are found in megakaryoblasts from nearly all individuals with Down syndrome with transient myeloproliferative disorder (TMD, also called transient leukemia) and the related acute megakaryoblastic leukemia (DS-AMKL, also called ...

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  • Increased LIS1 expression affects human and mouse brain development.

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  • A double-stranded RNA binding protein required for activation of repressed messages in mammalian germ cells.

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  • Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.

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    doi:10.1038/ng.2344

    authors: Emond MJ,Louie T,Emerson J,Zhao W,Mathias RA,Knowles MR,Wright FA,Rieder MJ,Tabor HK,Nickerson DA,Barnes KC,National Heart, Lung, and Blood Institute (NHLBI) GO Exome Sequencing Project.,Lung GO.,Gibson RL,Bamshad MJ

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  • Predicting the influence of common variants.

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  • Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families.

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  • Emergence and global spread of epidemic healthcare-associated Clostridium difficile.

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  • PHF6 mutations in T-cell acute lymphoblastic leukemia.

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    journal_title:Nature genetics

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  • Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production.

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    pub_type: 评论,新闻

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    authors: Gordon CT,Lyonnet S

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  • Improving grain yield, stress resilience and quality of bread wheat using large-scale genomics.

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    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/s41588-019-0496-6

    authors: Juliana P,Poland J,Huerta-Espino J,Shrestha S,Crossa J,Crespo-Herrera L,Toledo FH,Govindan V,Mondal S,Kumar U,Bhavani S,Singh PK,Randhawa MS,He X,Guzman C,Dreisigacker S,Rouse MN,Jin Y,Pérez-Rodríguez P,Montesinos-L

    更新日期:2019-10-01 00:00:00

  • Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.

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    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.623

    authors: Bezzina CR,Pazoki R,Bardai A,Marsman RF,de Jong JSSG,Blom MT,Scicluna BP,Jukema JW,Bindraban NR,Lichtner P,Pfeufer A,Bishopric NH,Roden DM,Meitinger T,Chugh SS,Myerburg RJ,Jouven X,Kääb S,Dekker LRC,Tan HL,Tanck M

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  • Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.

    abstract::17q11 microdeletions that encompass NF1 cause 5%-10% of cases of neurofibromatosis type 1, and individuals with microdeletions are typically taller than individuals with intragenic NF1 mutations, suggesting that deletion of a neighboring gene might promote human growth. We identified mutations in RNF135, which is with...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng2083

    authors: Douglas J,Cilliers D,Coleman K,Tatton-Brown K,Barker K,Bernhard B,Burn J,Huson S,Josifova D,Lacombe D,Malik M,Mansour S,Reid E,Cormier-Daire V,Cole T,Childhood Overgrowth Collaboration.,Rahman N

    更新日期:2007-08-01 00:00:00

  • Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.

    abstract::Overgrowth disorders are a heterogeneous group of conditions characterized by increased growth parameters and other variable clinical features such as intellectual disability and facial dysmorphism. To identify new causes of human overgrowth, we performed exome sequencing in ten proband-parent trios and detected two d...

    journal_title:Nature genetics

    pub_type: 杂志文章

    doi:10.1038/ng.2917

    authors: Tatton-Brown K,Seal S,Ruark E,Harmer J,Ramsay E,Del Vecchio Duarte S,Zachariou A,Hanks S,O'Brien E,Aksglaede L,Baralle D,Dabir T,Gener B,Goudie D,Homfray T,Kumar A,Pilz DT,Selicorni A,Temple IK,Van Maldergem L,Yac

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  • Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency.

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    doi:10.1038/ng0501-73

    authors: Lübke T,Marquardt T,Etzioni A,Hartmann E,von Figura K,Körner C

    更新日期:2001-05-01 00:00:00

  • Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions.

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    pub_type: 杂志文章

    doi:10.1038/s41588-018-0268-8

    authors: Urbut SM,Wang G,Carbonetto P,Stephens M

    更新日期:2019-01-01 00:00:00

  • Molecular landmarks of tumor hypoxia across cancer types.

    abstract::Many primary-tumor subregions have low levels of molecular oxygen, termed hypoxia. Hypoxic tumors are at elevated risk for local failure and distant metastasis, but the molecular hallmarks of tumor hypoxia remain poorly defined. To fill this gap, we quantified hypoxia in 8,006 tumors across 19 tumor types. In ten tumo...

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    pub_type: 杂志文章

    doi:10.1038/s41588-018-0318-2

    authors: Bhandari V,Hoey C,Liu LY,Lalonde E,Ray J,Livingstone J,Lesurf R,Shiah YJ,Vujcic T,Huang X,Espiritu SMG,Heisler LE,Yousif F,Huang V,Yamaguchi TN,Yao CQ,Sabelnykova VY,Fraser M,Chua MLK,van der Kwast T,Liu SK,Bout

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