Array Comparative Genomic Hybridization | List of Frontiers open access articles

Original Research

Published on 12 Dec 2019

Array Comparative Genomic Hybridization Analysis Reveals Significantly Enriched Pathways in Canine Oral Melanoma

in Cancer Genetics

Ginevra Brocca
Serena Ferraresso
Clarissa Zamboni
Elena M. Martinez-Merlo
Silvia Ferro
Michael H. Goldschmidt
Massimo Castagnaro

Frontiers in Oncology

doi 10.3389/fonc.2019.01397

6,163 views
18 citations

Original Research

Published on 09 Aug 2013

Microenvironment-Dependent Phenotypic Changes in a SCID Mouse Model for Malignant Mesothelioma

in Thoracic Oncology

Eva Darai-Ramqvist
Gustav Nilsonne
Carmen Flores-Staino
Anders Hjerpe
Katalin Dobra

Frontiers in Oncology

doi 10.3389/fonc.2013.00203

5,343 views
2 citations

Original Research

Published on 25 Mar 2022

Trypanosoma cruzi Genomic Variability: Array Comparative Genomic Hybridization Analysis of Clone and Parental Strain

in Parasite and Host

Danielle Rodrigues Cortez
Fabio Mitsuo Lima
João Luís Reis-Cunha
Daniella Castanheira Bartholomeu
Rolando Andre Rios Villacis
Silvia Regina Rogatto
André Guilherme Costa-Martins
Fernanda Sycko Marchiano
Rafaela Andrade do Carmo
Jose Franco da Silveira

Frontiers in Cellular and Infection Microbiology

doi 10.3389/fcimb.2022.760830

4,598 views
5 citations

Original Research

Published on 06 Jan 2026

Identification of the HMGA2::CIBAR1-DT fusion transcript in two lipomas with chromosomal rearrangements involving chromosomes 8 and 12

in Cancer Genetics

Marta Brunetti
Kristin Andersen
Ingvild Lobmaier
Francesca Micci

Frontiers in Oncology

doi 10.3389/fonc.2025.1717031

629 views

Case Report

Published on 21 Mar 2022

A de novo PUM1 Variant in a Girl With a Dravet-Like Syndrome: Case Report and Literature Review

in Pediatric Neurology

Yuanzhen Ye
Zhanqi Hu
Jiahui Mai
Li Chen
Dezhi Cao
Jianxiang Liao
Jing Duan

Frontiers in Pediatrics

doi 10.3389/fped.2022.759889

4,489 views
2 citations

Original Research

Published on 20 Mar 2024

NUP214 fusion genes in acute leukemias: genetic characterization of rare cases

in Hematologic Malignancies

Marta Brunetti
Kristin Andersen
Signe Spetalen
Andrea Lenartova
Liv Toril Nygård Osnes
Helen Vålerhaugen
Sverre Heim
Francesca Micci

Frontiers in Oncology

doi 10.3389/fonc.2024.1371980

3,722 views
3 citations

Case Report

Published on 23 Nov 2023

Case report: Familial case with autism spectrum and bipolar disorder showing a 20q11.21 microduplication including TM9SF4

in Autism

Marly Simoncini
Miriam Violi
Angelo Valetto
Veronica Bertini
Francy Cruz-Sanabria
Leonardo Massoni
Liliana Dell’Osso
Claudia Carmassi

Frontiers in Psychiatry

doi 10.3389/fpsyt.2023.1240663

3,560 views
1 citation

Original Research

Published on 07 Jan 2025

Prenatal ultrasound phenotype of fetuses with recurrent 1q21.1 deletion and duplication syndrome

in Genetics of Common and Rare Diseases

Fengyang Wang
Huijuan Peng
Guiyu Lou
Yanxin Ren
Shixiu Liao

Frontiers in Pediatrics

doi 10.3389/fped.2024.1504122

2,044 views
1 citation

Case Report

Published on 09 Oct 2017

Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease

in Genetics of Common and Rare Diseases

Fátima Lopes
Gabriela Soares
Miguel Gonçalves-Rocha
Jorge Pinto-Basto
Patrícia Maciel

Frontiers in Genetics

doi 10.3389/fgene.2017.00143

11,995 views
24 citations

Original Research

Published on 24 Feb 2021

Gene Set Enrichment Analysis of Interaction Networks Weighted by Node Centrality

in Computational Genomics

Alessandra Zito
Marta Lualdi
Paola Granata
Dario Cocciadiferro
Antonio Novelli
Tiziana Alberio
Rosario Casalone
Mauro Fasano

Frontiers in Genetics

doi 10.3389/fgene.2021.577623

35,190 views
58 citations

Case Report

Published on 12 Dec 2023

Primary biliary cholangitis with features of autoimmune hepatitis in a 19-year-old adolescent with 14q24.1q24.2 deletion: a case report

in Pediatric Gastroenterology, Hepatology and Nutrition

Yi-Wei Wang
Hsun-Chin Chao
Huei-Shyong Wang
Ju-Li Lin
Chih-Chen Chang
Shiu-Feng Huang

Frontiers in Pediatrics

doi 10.3389/fped.2023.1280409

3,796 views
1 citation

Original Research

Published on 31 Dec 2013

Next-Generation Sequencing of Disseminated Tumor Cells

in Molecular and Cellular Oncology

Elen Kristine Møller
Parveen Kumar
Thierry Voet
April Peterson
Peter Van Loo
Randi R. Mathiesen
Renathe Fjelldal
Jason Grundstad
Elin Borgen
Lars O. Baumbusch

Frontiers in Oncology

doi 10.3389/fonc.2013.00320

14,116 views
33 citations

Case Report

Published on 09 Jan 2023

Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay—Does both possibly act to modulate a candidate gene region for the patient’s phenotype?

in Genetics of Common and Rare Diseases

Rahma Touhami
Hajer Foddha
Eudeline Alix
Afef Jalloul
Soumaya Mougou-Zerelli
Ali Saad
Damien Sanlaville
Amel Haj Khelil

Frontiers in Genetics

doi 10.3389/fgene.2022.1061539

3,442 views
3 citations

Original Research

Published on 28 Oct 2022

OMIXCARE: OMICS technologies solved about 33% of the patients with heterogeneous rare neuro-developmental disorders and negative exome sequencing results and identified 13% additional candidate variants

in Molecular and Cellular Pathology

Estelle Colin
Yannis Duffourd
Emilie Tisserant
Raissa Relator
Ange-Line Bruel
Frédéric Tran Mau-Them
Anne-Sophie Denommé-Pichon
Hana Safraou
Julian Delanne
Nolwenn Jean-Marçais

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2022.1021785

6,079 views
16 citations

Case Report

Published on 20 Nov 2019

Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities

in Genetics of Common and Rare Diseases

Anna A. Pendina
Yulia V. Shilenkova
Olga E. Talantova
Olga A. Efimova
Olga G. Chiryaeva
Olga V. Malysheva
Vera S. Dudkina
Lubov' I. Petrova
Elena A. Serebryakova
Elena S. Shabanova

Frontiers in Genetics

doi 10.3389/fgene.2019.01164

5,331 views
8 citations

Original Research

Published on 23 Feb 2023

Integrating copy number data of 64 iAMP21 BCP-ALL patients narrows the common region of amplification to 1.57 Mb

in Hematologic Malignancies

Femke M. Hormann
Alex Q. Hoogkamer
Aurélie Boeree
Edwin Sonneveld
Gabriele Escherich
Monique L. den Boer
Judith M. Boer

Frontiers in Oncology

doi 10.3389/fonc.2023.1128560

3,461 views
6 citations

Articles

Array Comparative Genomic Hybridization Analysis Reveals Significantly Enriched Pathways in Canine Oral Melanoma

Microenvironment-Dependent Phenotypic Changes in a SCID Mouse Model for Malignant Mesothelioma

Trypanosoma cruzi Genomic Variability: Array Comparative Genomic Hybridization Analysis of Clone and Parental Strain

Identification of the HMGA2::CIBAR1-DT fusion transcript in two lipomas with chromosomal rearrangements involving chromosomes 8 and 12

A de novo PUM1 Variant in a Girl With a Dravet-Like Syndrome: Case Report and Literature Review

NUP214 fusion genes in acute leukemias: genetic characterization of rare cases

Case report: Familial case with autism spectrum and bipolar disorder showing a 20q11.21 microduplication including TM9SF4

Prenatal ultrasound phenotype of fetuses with recurrent 1q21.1 deletion and duplication syndrome

Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease

Gene Set Enrichment Analysis of Interaction Networks Weighted by Node Centrality

Primary biliary cholangitis with features of autoimmune hepatitis in a 19-year-old adolescent with 14q24.1q24.2 deletion: a case report

Next-Generation Sequencing of Disseminated Tumor Cells

Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay—Does both possibly act to modulate a candidate gene region for the patient’s phenotype?

OMIXCARE: OMICS technologies solved about 33% of the patients with heterogeneous rare neuro-developmental disorders and negative exome sequencing results and identified 13% additional candidate variants

Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities

Integrating copy number data of 64 iAMP21 BCP-ALL patients narrows the common region of amplification to 1.57 Mb