Publications by authors named "Anne-Katrin Emde"

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Clinical trajectories and genetic profiles of SOD1-related amyotrophic lateral sclerosis: insights from a single-center cohort in India.
Muddasu Suhasini Keerthipriya, Ananthapadmanabha Kotambail, Madhusudhan Deekshitha, R Mahima, M B Ramyashree, Anne-Katrin Emde

J Neurol· January 2026

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Mid-pass whole-genome sequencing in a Malagasy cohort uncovers body composition associations.
Iman Hamid, Séverine Nantenaina Stéphie Raveloson, Germain Jules Spiral, Soanorolalao Ravelonjanahary, Brigitte Marie Raharivololona, Anne-Katrin Emde

HGG Adv· July 2025

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A map of blood regulatory variation in South Africans enables GWAS interpretation.
Stephane E Castel, Furahini D Tluway, Anne-Katrin Emde, Natalie Smyth, Mohd Karim

Nat Genet· July 2025

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Mid-pass whole-genome sequencing in a Malagasy cohort uncovers body composition associations.
Iman Hamid, Séverine Nantenaina Stéphie Raveloson, Germain Jules Spiral, Soanorolalao Ravelonjanahary, Brigitte Marie Raharivololona, Anne-Katrin Emde

HGG Adv· October 2024

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The gout epidemic in French Polynesia: a modelling study of data from the Ma'i u'u epidemiological survey.
Tristan Pascart, Kaja A Wasik, Cristian Preda, Valérie Chune, Jérémie Torterat, Anne-Katrin Emde

Lancet Glob Health· April 2024

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Somatic whole genome dynamics of precancer in Barrett's esophagus reveals features associated with disease progression.
Thomas G Paulson, Patricia C Galipeau, Kenji M Oman, Carissa A Sanchez, Mary K Kuhner, Anne-Katrin Emde

Nat Commun· April 2022

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Diverse tumorigenic consequences of human papillomavirus integration in primary oropharyngeal cancers.
David E Symer, Keiko Akagi, Heather M Geiger, Yang Song, Gaiyun Li, Anne-Katrin Emde

Genome Res· January 2022

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Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations.
Anne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, C Scott Gallagher, Tanya J Major

BMC Genomics· November 2021

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Daniel Taliun, Daniel N Harris, Michael D Kessler, Jedidiah Carlson, Zachary A Szpiech, Anne-Katrin Emde

Nature· February 2021

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Author Correction: PGBD5 promotes site-specific oncogenic mutations in human tumors.
Anton G Henssen, Richard Koche, Jiali Zhuang, Eileen Jiang, Casie Reed, Anne-Katrin Emde

Nat Genet· November 2020

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Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs.
Kevin Hadi, Xiaotong Yao, Julie M Behr, Aditya Deshpande, Charalampos Xanthopoulakis, Anne-Katrin Emde

Cell· October 2020

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Genetic mechanisms of primary chemotherapy resistance in pediatric acute myeloid leukemia.
Nicole A McNeer, John Philip, Heather Geiger, Rhonda E Ries, Vincent-Philippe Lavallée, Anne-Katrin Emde

Leukemia· August 2019

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Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.
Mayu O Frank, Takahiko Koyama, Kahn Rhrissorrakrai, Nicolas Robine, Filippo Utro, Anne-Katrin Emde

BMC Med Genomics· August 2019

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Sequencing and curation strategies for identifying candidate glioblastoma treatments.
Mayu O Frank, Takahiko Koyama, Kahn Rhrissorrakrai, Nicolas Robine, Filippo Utro, Anne-Katrin Emde

BMC Med Genomics· April 2019

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Human papillomavirus and the landscape of secondary genetic alterations in oral cancers.
Maura L Gillison, Keiko Akagi, Weihong Xiao, Bo Jiang, Robert K L Pickard, Anne-Katrin Emde

Genome Res· January 2019

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Whole Genome Sequencing-Based Discovery of Structural Variants in Glioblastoma.
Kazimierz O Wrzeszczynski, Vanessa Felice, Minita Shah, Sadia Rahman, Anne-Katrin Emde

Methods Mol Biol· December 2018

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Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer.
Kazimierz O Wrzeszczynski, Vanessa Felice, Avinash Abhyankar, Lukasz Kozon, Heather Geiger, Anne-Katrin Emde

J Mol Diagn· November 2018

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Genome-wide somatic variant calling using localized colored de Bruijn graphs.
Giuseppe Narzisi, André Corvelo, Kanika Arora, Ewa A Bergmann, Minita Shah, Anne-Katrin Emde

Commun Biol· March 2018

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Erratum: PGBD5 promotes site-specific oncogenic mutations in human tumors.
Anton G Henssen, Richard Koche, Jiali Zhuang, Eileen Jiang, Casie Reed, Anne-Katrin Emde

Nat Genet· September 2017

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Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.
Kazimierz O Wrzeszczynski, Mayu O Frank, Takahiko Koyama, Kahn Rhrissorrakrai, Nicolas Robine, Anne-Katrin Emde

Neurol Genet· August 2017

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PGBD5 promotes site-specific oncogenic mutations in human tumors.
Anton G Henssen, Richard Koche, Jiali Zhuang, Eileen Jiang, Casie Reed, Anne-Katrin Emde

Nat Genet· July 2017

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Next-Generation Rapid Autopsies Enable Tumor Evolution Tracking and Generation of Preclinical Models.
David J Pisapia, Steven Salvatore, Chantal Pauli, Erika Hissong, Ken Eng, Anne-Katrin Emde

JCO Precis Oncol· June 2017

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Whole-Exome Sequencing of Metastatic Cancer and Biomarkers of Treatment Response.
Himisha Beltran, Kenneth Eng, Juan Miguel Mosquera, Alexandros Sigaras, Alessandro Romanel, Anne-Katrin Emde

JAMA Oncol· July 2015

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Disease variants in genomes of 44 centenarians.
Yun Freudenberg-Hua, Jan Freudenberg, Vladimir Vacic, Avinash Abhyankar, Anne-Katrin Emde

Mol Genet Genomic Med· September 2014

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Comparative sequencing analysis reveals high genomic concordance between matched primary and metastatic colorectal cancer lesions.
A Rose Brannon, Efsevia Vakiani, Brooke E Sylvester, Sasinya N Scott, Gregory McDermott, Anne-Katrin Emde

Genome Biol· August 2014

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