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Genetic signatures of exceptional longevity in humans

PloS one, 2012-01, Vol.7 (1), p.e29848

2012

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Survival and low-grade glioma: the emergence of genetic information

Neurosurgical focus, 2015-01, Vol.38 (1), p.E6-E6

2015

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The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer

Science (American Association for the Advancement of Science), 2015-05, Vol.348 (6238), p.1036-1039

2015

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Accelerated epigenetic aging in newborns with Down syndrome

Aging cell, 2022-07, Vol.21 (7), p.e13652-n/a

2022

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Disruption of the β1L Isoform of GABP Reverses Glioblastoma Replicative Immortality in a TERT Promoter Mutation-Dependent Manner

Cancer cell, 2018-09, Vol.34 (3), p.513-528.e8

2018

Volltextzugriff (PDF)

Localized variation in ancestral admixture identifies pilocytic astrocytoma risk loci among Latino children

PLoS genetics, 2022-09, Vol.18 (9), p.e1010388-e1010388

2022

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GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21

Nature communications, 2018-01, Vol.9 (1), p.286-8, Article 286

2018

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Maternal Fc-mediated non-neutralizing antibody responses correlate with protection against congenital human cytomegalovirus infection

The Journal of clinical investigation, 2022-08, Vol.132 (16), p.1-15

2022

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The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis

Nature communications, 2021-02, Vol.12 (1), p.821-15, Article 821

2021

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Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation Process

Cancer research (Chicago, Ill.), 2016-11, Vol.76 (22), p.6680-6689

2016

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Shared genomic architecture between COVID-19 severity and numerous clinical and physiologic parameters revealed by LD score regression analysis

Scientific reports, 2022-02, Vol.12 (1), p.1891-1891, Article 1891

2022

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The shared genetic architecture between epidemiological and behavioral traits with lung cancer

Scientific reports, 2021-09, Vol.11 (1), p.17559-12, Article 17559

2021

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Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk

Cancer science, 2019-06, Vol.110 (6), p.2022-2032

2019

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Telomere Attrition in Childhood Cancer Survivors

Clinical cancer research, 2020-05, Vol.26 (10), p.2281-2283

Walsh, Kyle M

2020

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Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

BMC pregnancy and childbirth, 2012-06, Vol.12 (1), p.61-61, Article 61

2012

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Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas

Neuro-oncology (Charlottesville, Va.), 2018-04, Vol.20 (5), p.632-641

2018

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A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution

Cancer research (Chicago, Ill.), 2015-11, Vol.75 (22), p.4884-4894

2015

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[ 18 F]-fluoroethyl-L-tyrosine (FET) in glioblastoma (FIG) TROG 18.06 study: protocol for a prospective, multicentre PET/CT trial

BMJ open, 2023-08, Vol.13 (8), p.e071327-e071327

2023

Volltextzugriff (PDF)

Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: A systematic review and meta-analysis

Genetics in medicine, 2011-05, Vol.13 (5), p.377-384

2011

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Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates

Epigenetics, 2016-09, Vol.11 (9), p.664-673

2016

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To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes

Frontiers in genetics, 2018-08, Vol.9, p.298-298

2018

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ADCC-activating antibodies correlate with decreased risk of congenital human cytomegalovirus transmission

JCI insight, 2023-07, Vol.8 (13)

2023

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Assisted reproductive technology and association with childhood cancer subtypes

Cancer medicine (Malden, MA), 2023-02, Vol.12 (3), p.3410-3418

2023

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Coexisting Biopsy-Diagnosed Dementia and Glioblastoma

Brain sciences, 2024-01, Vol.14 (2), p.143

2024

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Epidemiology of meningiomas

Handbook of Clinical Neurology, 2020, Vol.169, p.3-15

Walsh, Kyle M.

2020

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Genetic signatures of exceptional longevity in humans

Survival and low-grade glioma: the emergence of genetic information

The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer

Accelerated epigenetic aging in newborns with Down syndrome

Disruption of the β1L Isoform of GABP Reverses Glioblastoma Replicative Immortality in a TERT Promoter Mutation-Dependent Manner

Localized variation in ancestral admixture identifies pilocytic astrocytoma risk loci among Latino children

GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21

Maternal Fc-mediated non-neutralizing antibody responses correlate with protection against congenital human cytomegalovirus infection

The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis

Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation Process

Shared genomic architecture between COVID-19 severity and numerous clinical and physiologic parameters revealed by LD score regression analysis

The shared genetic architecture between epidemiological and behavioral traits with lung cancer

Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk

Telomere Attrition in Childhood Cancer Survivors

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas

A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution

[ 18 F]-fluoroethyl-L-tyrosine (FET) in glioblastoma (FIG) TROG 18.06 study: protocol for a prospective, multicentre PET/CT trial

Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: A systematic review and meta-analysis

Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates

To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes

ADCC-activating antibodies correlate with decreased risk of congenital human cytomegalovirus transmission

Assisted reproductive technology and association with childhood cancer subtypes

Coexisting Biopsy-Diagnosed Dementia and Glioblastoma

Epidemiology of meningiomas

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