Sara Seneca - the Dutch-Speaking Brussels Free University, Vrije Universiteit Brussel

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论文共 280 篇作者统计合作学者相似作者

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Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult Patients

PEDIATRIC NEUROLOGY (2024): 57-65

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Children Born after Assisted Reproduction More Commonly Carry a Mitochondrial Genotype Associating with Low Birthweight

Joke Mertens,Florence Belva,Aafke P. A. van Montfoort,Marius Regin,Filippo Zambelli,Sara Seneca,Edouard Couvreu de Deckersberg,Maryse Bonduelle,Herman Tournaye,Katrien Stouffs,Kurt Barbé,Hubert J. M. Smeets,Hilde Van de Velde,Karen Sermon,Christophe Blockeel,Claudia Spits

NATURE COMMUNICATIONS（2024）

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Identification of RAD17 As a Candidate Cancer Predisposition Gene in Families with Histories of Pancreatic and Breast Cancers

Sofie Joris,Philippe Giron,Catharina Olsen,Sara Seneca,Alexander Gheldof, Shula Staessens,Rajendra Bahadur Shahi,Sylvia De Brakeleer,Erik Teugels,Jacques De Grève, Frederik J. Hes

BMC Cancerno. 1 (2024)

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Protein-coding and Rrna Variants Drive a Mitochondrial DNA Genotype That Associates to Low Birth Weight and is More Common in Individuals Born after Assisted Reproductive Technologies

Joke Mertens,Florence Belva,Aafke van Montfoort,Filippo Zambelli,Sara Seneca,Edouard Couvreu de Deckersberg,Maryse Bonduelle,Herman Tournaye,Katrien Stouffs,Kurt Barbé,Hubert Smeets,Hilde Van de Velde,Karen Sermon,Christophe Blockeel,Claudia Spits

openalex（2023）

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Belgian guidelines for the frequency of participation of the Medical Centers of Human Genetics to External Quality Assessment schemes for analyses focused on rare diseases

Josephine Lantoine,Anne Brysse,Vinciane Dideberg,Kathleen B. M. Claes,Sofie Symoens,Wim Coucke,Valerie Benoit,Sonia Rombout,Martine De Rycke,Sara Seneca,Lut Van Laer,Wim Wuyts,Anniek Corveleyn,Kris Van den Bogaert, Catherine Rydlewski, Francoise Wilkin,Marie Ravoet,Elodie Fastre,Arnaud Capron,Nathalie M. Vandevelde

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Computation of a database of interspersed repeats in coding regions of the human genome

Doan T. L. Vo Ngoc,Randy Osei, Katrien Dohr,Catharina Olsen,Katrien Stouffs,Karen Sermon,Sara Seneca,Alexander Gheldof

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype—Different Onset

Sara Capiau,Joel Smet,Boel De Paepe,Yilmaz Yildiz,Mutluay Arslan,Olivier Stevens,Maxime Verschoore,Hedwig Stepman,Sara Seneca,Arnaud Vanlander

Cells（2022）

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Differences in Maternally Inherited and Age-Related De Novo Mitochondrial DNA Variants Between ART and Spontaneously Conceived Individuals Associate with Low Birth Weight

Joke Mertens,Florence Belva,Aafke P.A. van Montfoort,Filippo Zambelli,Sara Seneca,Edouard Couvreu de Deckersberg,Maryse Bonduelle,Herman Tournaye,Katrien Stouffs,Kurt Barbé,Hubert Smeets,Hilde Van de Velde,Karen Sermon,Christophe Blockeel,Claudia Spits

crossref（2022）

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Primary Ovarian Insufficiency in RMND1 Mitochondrial Disease

Emese Boros, Mawa Ongoth Farel Elilie,Claudine Heinrichs,Anne Laure Mansbach,Sara Seneca,Alec Aeby,Khalid Ismaïli,Cécile Brachet

Endocrine Abstracts（2022）

引用3浏览0引用

EDIR: Exome Database of Interspersed Repeats

Laura D. T. Vo Ngoc,Randy Osei,Katrin Dohr,Catharina Olsen,Sara Seneca,Alexander Gheldof

Bioinformatics（2022）

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