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driveR: a novel method for prioritizing cancer driver genes using somatic genomics data

BMC bioinformatics, 2021-05, Vol.22 (1), p.1-263, Article 263

2021

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Endometrial gene expression profiling of recurrent implantation failure after in vitro fertilization

Molecular biology reports, 2021-06, Vol.48 (6), p.5075-5082

2021

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CogNet: classification of gene expression data based on ranked active-subnetwork-oriented KEGG pathway enrichment analysis

PeerJ. Computer science, 2021-02, Vol.7, p.e336-e336, Article e336

2021

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A microdeletion event at 19q13.43 in IDH-mutant astrocytomas is strongly correlated with MYC overexpression

Acta neuropathologica communications, 2024-06, Vol.12 (1), p.95-11, Article 95

2024

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Correlation of anatomical involvement patterns of insular gliomas with subnetworks of the limbic system

Journal of neurosurgery, 2022-02, Vol.136 (2), p.323-334

2022

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Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas

Journal of neurosurgery, 2018-04, Vol.128 (4), p.1102-1114

2018

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Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas

Journal of neurosurgery, 2020-05, Vol.132 (5), p.1435-1446

2020

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Gene pathway analysis of the endometrium at the start of the window of implantation in women with unexplained infertility and unexplained recurrent pregnancy loss: is unexplained recurrent pregnancy loss a subset of unexplained infertility?

Human fertility (Cambridge, England), 2023-12, Vol.ahead-of-print (ahead-of-print), p.1-13

2023

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Meningiomas Display a Specific Immunoexpression Pattern in a Rostrocaudal Gradient: An Analysis of 366 Patients

World neurosurgery, 2019-03, Vol.123, p.e520-e535

2019

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Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data

PeerJ (San Francisco, CA), 2021-09, Vol.9, p.e11922, Article e11922

2021

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Comparison of endometrial prostanoid profiles in three infertile subgroups: the missing part of receptivity?

Fertility and sterility, 2020-03, Vol.113 (3), p.670-678.e1

2020

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Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

BMC medical genomics, 2021-02, Vol.14 (1), p.54-14, Article 54

2021

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IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation

Scientific reports, 2016-06, Vol.6 (1), p.27569-27569, Article 27569

2016

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pathfindR: An R Package for Comprehensive Identification of Enriched Pathways in Omics Data Through Active Subnetworks

Frontiers in genetics, 2019-09, Vol.10, p.858-858

2019

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Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms

Biomedicines, 2020-12, Vol.8 (12), p.574

2020

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A comparison of various feature extraction and machine learning methods for antimicrobial resistance prediction in streptococcus pneumoniae

Frontiers in antibiotics, 2023-03, Vol.2

2023

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PANACEA: network-based methods for pharmacotherapy prioritization in personalized oncology

Bioinformatics (Oxford, England), 2023-01, Vol.39 (1)

2023

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Potential Marker Pathways in the Endometrium That May Cause Recurrent Implantation Failure

Reproductive sciences (Thousand Oaks, Calif.), 2019-07, Vol.26 (7), p.879-890

2019

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A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon

European journal of paediatric neurology, 2015-11, Vol.19 (6), p.743-746

2015

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Integrated bioinformatics analysis of validated and circulating miRNAs in ovarian cancer

Genomics & informatics, 2022, Vol.20 (2), p.20.1-20.13

2022

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Integrated bioinformatics analysis of validated and circulating miRNAs in ovarian cancer

Genomics & informatics, 2022-06, Vol.20 (2), p.e20-e20

2022

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Clinical, Electrodiagnostic, and Genetic Features of Tangier Disease in an Adolescent Girl with Presentation of Peripheral Neuropathy

Neuropediatrics, 2015-12, Vol.46 (6), p.420

2015

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ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features

Cold Spring Harbor molecular case studies, 2017-09, Vol.3 (5), p.a001859

2017

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Innovative Use of an Injectable, Self-Healing Drug-Loaded Pectin-Based Hydrogel for Micro- and Supermicro-Vascular Anastomoses

Biomacromolecules, 2024-07, Vol.25 (7), p.3959-3975

2024

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driveR: a novel method for prioritizing cancer driver genes using somatic genomics data

Endometrial gene expression profiling of recurrent implantation failure after in vitro fertilization

CogNet: classification of gene expression data based on ranked active-subnetwork-oriented KEGG pathway enrichment analysis

A microdeletion event at 19q13.43 in IDH-mutant astrocytomas is strongly correlated with MYC overexpression

Correlation of anatomical involvement patterns of insular gliomas with subnetworks of the limbic system

Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas

Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas

Gene pathway analysis of the endometrium at the start of the window of implantation in women with unexplained infertility and unexplained recurrent pregnancy loss: is unexplained recurrent pregnancy loss a subset of unexplained infertility?

Meningiomas Display a Specific Immunoexpression Pattern in a Rostrocaudal Gradient: An Analysis of 366 Patients

Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data

Comparison of endometrial prostanoid profiles in three infertile subgroups: the missing part of receptivity?

Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation

pathfindR: An R Package for Comprehensive Identification of Enriched Pathways in Omics Data Through Active Subnetworks

Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms

A comparison of various feature extraction and machine learning methods for antimicrobial resistance prediction in streptococcus pneumoniae

PANACEA: network-based methods for pharmacotherapy prioritization in personalized oncology

Potential Marker Pathways in the Endometrium That May Cause Recurrent Implantation Failure

A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon

Integrated bioinformatics analysis of validated and circulating miRNAs in ovarian cancer

Integrated bioinformatics analysis of validated and circulating miRNAs in ovarian cancer

Clinical, Electrodiagnostic, and Genetic Features of Tangier Disease in an Adolescent Girl with Presentation of Peripheral Neuropathy

ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features

Innovative Use of an Injectable, Self-Healing Drug-Loaded Pectin-Based Hydrogel for Micro- and Supermicro-Vascular Anastomoses

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