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Strelka: accurate somatic small-variant calling from sequenced tumor―normal sample pairs

Bioinformatics, 2012-07, Vol.28 (14), p.1811-1817

2012

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Rate of de novo mutations and the importance of father's age to disease risk

Nature (London), 2012-08, Vol.488 (7412), p.471-475

2012

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Accuracy and Power of Statistical Methods for Detecting Adaptive Evolution in Protein Coding Sequences and for Identifying Positively Selected Sites

Genetics (Austin), 2004-10, Vol.168 (2), p.1041-1051

2004

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Protein interaction networks define the genetic architecture of preterm birth

Scientific reports, 2022-01, Vol.12 (1), p.438-438, Article 438

2022

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Parent-of-origin-specific signatures of de novo mutations

Nature genetics, 2016-08, Vol.48 (8), p.935-939

2016

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Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

Nature genetics, 2018-04, Vol.50 (4), p.487-492

2018

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New observations on maternal age effect on germline de novo mutations

Nature communications, 2016-01, Vol.7 (1), p.10486-10486, Article 10486

2016

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Detecting Selection in Noncoding Regions of Nucleotide Sequences

Genetics (Austin), 2004-06, Vol.167 (2), p.949-958

2004

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Publisher Correction: Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

Nature genetics, 2021-08, Vol.53 (8), p.1270-1270

2021

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Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity

Genome research, 2021-09, Vol.31 (9), p.1513

2021

Volltextzugriff (PDF)

Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling

Human mutation, 2018-10, Vol.39 (10), p.1416-1427

2018

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Clinical and social factors associated with excess weight in Hispanic and non-Hispanic White children

Pediatric research, 2019-02, Vol.85 (3), p.256-261

2019

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Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers

Genes and immunity, 2020-01, Vol.21 (1), p.27-36

2020

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Finding cis-regulatory modules in Drosophila using phylogenetic hidden Markov models

Bioinformatics, 2007-08, Vol.23 (16), p.2031-2037

2007

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The Microbiome in Necrotizing Enterocolitis: A Case Report in Twins and Minireview

Clinical therapeutics, 2016-04, Vol.38 (4), p.747-753

2016

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BAP1 loss defines a new class of renal cell carcinoma

Nature genetics, 2012-07, Vol.44 (7), p.751-759

2012

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A Child’s HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus

Journal of autoimmunity, 2016-11, Vol.74, p.201-207

2016

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Identification of physicochemical selective pressure on protein encoding nucleotide sequences

BMC bioinformatics, 2006-03, Vol.7 (1), p.148-148, Article 148

2006

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Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates

Genetics in medicine, 2016-03, Vol.18 (3), p.221-230

2016

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Genomic and molecular characterization of preterm birth

Proceedings of the National Academy of Sciences - PNAS, 2019-03, Vol.116 (12), p.5819-5827

2019

Volltextzugriff (PDF)

Bayes empirical bayes inference of amino acid sites under positive selection

Molecular biology and evolution, 2005-04, Vol.22 (4), p.1107-1118

2005

Volltextzugriff (PDF)

Moving Toward Findable, Accessible, Interoperable, Reusable Practices in Epidemiologic Research

American journal of epidemiology, 2023-06, Vol.192 (6), p.995-1005

2023

Volltextzugriff (PDF)

ArCH: improving the performance of clonal hematopoiesis variant calling and interpretation

Bioinformatics (Oxford, England), 2024-03, Vol.40 (4)

2024

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Gut microbial composition difference between pediatric ALL survivors and siblings

Pediatric hematology and oncology, 2020-08, Vol.37 (6), p.475-488

2020

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Differences in maternal gene expression in Cesarean section delivery compared with vaginal delivery

Scientific reports, 2020-10, Vol.10 (1), p.17797, Article 17797

2020

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Strelka: accurate somatic small-variant calling from sequenced tumor―normal sample pairs

Rate of de novo mutations and the importance of father's age to disease risk

Accuracy and Power of Statistical Methods for Detecting Adaptive Evolution in Protein Coding Sequences and for Identifying Positively Selected Sites

Protein interaction networks define the genetic architecture of preterm birth

Parent-of-origin-specific signatures of de novo mutations

Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

New observations on maternal age effect on germline de novo mutations

Detecting Selection in Noncoding Regions of Nucleotide Sequences

Publisher Correction: Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence

Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity

Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling

Clinical and social factors associated with excess weight in Hispanic and non-Hispanic White children

Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers

Finding cis-regulatory modules in Drosophila using phylogenetic hidden Markov models

The Microbiome in Necrotizing Enterocolitis: A Case Report in Twins and Minireview

BAP1 loss defines a new class of renal cell carcinoma

A Child’s HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus

Identification of physicochemical selective pressure on protein encoding nucleotide sequences

Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates

Genomic and molecular characterization of preterm birth

Bayes empirical bayes inference of amino acid sites under positive selection

Moving Toward Findable, Accessible, Interoperable, Reusable Practices in Epidemiologic Research

ArCH: improving the performance of clonal hematopoiesis variant calling and interpretation

Gut microbial composition difference between pediatric ALL survivors and siblings

Differences in maternal gene expression in Cesarean section delivery compared with vaginal delivery

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