Paul Brady

1.6k citations

27 papers · 981 · h-index 18

Impact in

Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Surgery top 10%
- Congenital Diaphragmatic Hernia Studies
- Congenital Anomalies and Fetal Surgery

Papers in

Surgery 12
- Congenital Diaphragmatic Hernia Studies 12
- Congenital Anomalies and Fetal Surgery 2
Molecular Biology 8
- Congenital heart defects research 5

Co-authors: Joris Vermeesch (20 shared papers)Jan Deprest (16 shared papers)Koenraad Devriendt (14 shared papers)E. Gratacós (3 shared papers)Hilde Van Esch (4 shared papers)Eric Legius (3 shared papers)Nathalie Brison (3 shared papers)Thomy de Ravel (3 shared papers)
Journals: Prenatal Diagnosis (5 papers)Seminars in Fetal and Neonatal Medicine (3 papers)European Journal of Human Genetics (3 papers)European Journal of Medical Genetics (2 papers)Neurology (1 paper)
Partner nations: Belgium United States India

In The Last Decade

Paul Brady

27 papers receiving 926 citations

Peers

Countries citing papers authored by Paul Brady

Since Specialization

Citations

This map shows the geographic impact of Paul Brady's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Paul Brady with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul Brady more than expected).

Fields of papers citing papers by Paul Brady

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul Brady. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Paul Brady. The network helps show where Paul Brady may publish in the future.

Co-authors

The 25 scholars most cited alongside Paul Brady, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Paul Brady Line = papers co-authored together Paul Brady links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing JAMA Oncology ·Frédéric Amant, Magali Verheecke, Iwona Włodarska, Luc Dehaspe, Paul Brady, Nathalie Brison, Kris Van Den Bogaert, Daan Dierickx, Vincent Vandecaveye, Thomas Tousseyn, Philippe Moerman, Adriaan Vanderstichele, Ignace Vergote, Patrick Neven, Patrick Berteloot, Katrien Putseys, Lode Danneels, Peter Vandenberghe, Eric Legius, Joris Vermeesch	2015	138
2	Prenatal management of the fetus with isolated congenital diaphragmatic hernia in the era of the TOTAL trial Seminars in Fetal and Neonatal Medicine ·Jan Deprest, Paul Brady, K. H. Nicolaides, Alexandra Benachi, Christoph Berg, Joris Vermeesch, Glenn Gardener, E. Gratacós	2014	110
3	Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management European Journal of Human Genetics ·Baran Bayindir, Luc Dehaspe, Nathalie Brison, Paul Brady, Simon Ardui, Molka Kammoun, Lars van der Veken, Klaske D. Lichtenbelt, Kris Van Den Bogaert, Jeroen Van Houdt, Hilde Peeters, Hilde Van Esch, Thomy de Ravel, Eric Legius, Koenraad Devriendt, Joris Vermeesch	2015	101
4	Clinical implementation of NIPT – technical and biological challenges Clinical Genetics ·Paul Brady, Nathalie Brison, K Van Den Bogaert, Thomy de Ravel, Hilde Peeters, Hilde Van Esch, Koenraad Devriendt, Eric Legius, Joris Vermeesch	2015	74
5	A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors Genetics in Medicine ·Paul Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Björn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, E Sleurs, Kathelijn Keymolen, Luc De Catte, Jan Deprest, Thomy de Ravel, Hilde Van Esch, J. P. Fryns, Koenraad Devriendt, Joris Vermeesch	2013	65
6	Genome-wide arrays: Quality criteria and platforms to be used in routine diagnostics Human Mutation ·Joris Vermeesch, Paul Brady, Damien Sanlaville, Klaas Kok, Rosalind J. Hastings	2012	59
7	Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH) Prenatal Diagnosis ·Kasemsri Srisupundit, Paul Brady, Koenraad Devriendt, Jean‐Pierre Fryns, R. Cruz‐Martínez, E. Gratacós, Jan Deprest, Joris Vermeesch	2010	43
8	Genomic microarrays: a technology overview Prenatal Diagnosis ·Paul Brady, Joris Vermeesch	2012	42
9	Fetal surgery is a clinical reality Seminars in Fetal and Neonatal Medicine ·Jan Deprest, Roland Devlieger, Kasemsri Srisupundit, Veronika Beck, Inga Sandaite, Silvia Rusconi, Filip Claus, Gunnar Naulaers, Marc Van de Velde, Paul Brady, Koenraad Devriendt, Joris Vermeesch, Jaan Toelen, Marianne Carlon, Zeger Debyser, Luc De Catte, Liesbeth Lewi	2009	38
10	Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia European Journal of Medical Genetics ·Paul Brady, Philippe Moerman, Luc De Catte, Jan Deprest, Koenraad Devriendt, Joris Vermeesch	2014	35
11	Recent Developments in the Genetic Factors Underlying Congenital Diaphragmatic Hernia Fetal Diagnosis and Therapy ·Paul Brady, Kasemsri Srisupundit, Koenraad Devriendt, Jean‐Pierre Fryns, Jan Deprest, Joris Vermeesch	2010	32
12	Identification of dosage‐sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia Prenatal Diagnosis ·Paul Brady, Philip DeKoninck, J. P. Fryns, Koenraad Devriendt, Jan Deprest, Joris Vermeesch	2013	32
13	Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next‐generation sequencing Prenatal Diagnosis ·Molka Kammoun, Erika Souche, Paul Brady, Jia Ding, Nele Cosemans, E. Gratacós, Koenraad Devriendt, E. Eixarch, Jan Deprest, Joris Vermeesch	2018	30
14	Expanding the phenotypic spectrum of PORCN variants in two males with syndromic microphthalmia European Journal of Human Genetics ·Paul Brady, Hilde Van Esch, Nathalie Fieremans, Guy Froyen, Anne Slavotinek, Jan Deprest, Koenraad Devriendt, Joris Vermeesch	2014	22
15	Primary Posterior Fossa Lesions and Preserved Supratentorial Cerebral Blood Flow: Implications for Brain Death Determination Neurocritical Care ·Panayiotis N. Varelas, Paul Brady, Mohammed Rehman, Arash Afshinnik, Chandan Mehta, Tamer Abdelhak, Eelco F. M. Wijdicks	2017	20
16	Transcriptome Analysis of the Preterm Rabbit Lung after Seven Days of Hyperoxic Exposure PLoS ONE ·Thomas Salaets, Jute Richter, Paul Brady, Julio Jiménez, Taro Nagatomo, Jan Deprest, Jaan Toelen	2015	20
17	Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury Journal of Translational Medicine ·Jute Richter, Julio Jiménez, Taro Nagatomo, Jaan Toelen, Paul Brady, Thomas Salaets, Flore Lesage, Jeroen Vanoirbeek, Jan Deprest	2016	18
18	Array technology in prenatal diagnosis Seminars in Fetal and Neonatal Medicine ·Orsetta Zuffardi, Annalisa Vetro, Paul Brady, Joris Vermeesch	2011	18
19	Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations European Journal of Medical Genetics ·Paul Brady, Jeroen Van Houdt, Bert Callewaert, Jan Deprest, Koenraad Devriendt, Joris Vermeesch	2014	16
20	Pulmonary transcriptome analysis in the rabbit model of surgically-induced diaphragmatic hernia treated with fetal tracheal occlusion Disease Models & Mechanisms ·Alexander Engels, Paul Brady, Molka Kammoun, (unknown), Philip DeKoninck, Masayuki Endo, Jaan Toelen, Joris Vermeesch, Jan Deprest	2016	16

About Paul Brady

Paul Brady is a scholar working on Surgery, Molecular Biology, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Genetics, having authored 27 papers that have together received 981 indexed citations. Recurring topics across this work include Congenital Diaphragmatic Hernia Studies (12 papers), Prenatal Screening and Diagnostics (7 papers), Neonatal Respiratory Health Research (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Organ Donation and Transplantation (4 papers) and Congenital Anomalies and Fetal Surgery (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (357 citations), Surgery (349 citations), Genetics (236 citations), Pulmonary and Respiratory Medicine (205 citations) and Cancer Research (91 citations). Paul Brady has collaborated with scholars based in Belgium, United States and India. Frequent co-authors include Joris Vermeesch, Jan Deprest, Koenraad Devriendt, E. Gratacós, Hilde Van Esch, Eric Legius, Nathalie Brison, Thomy de Ravel, Kris Van Den Bogaert and Hilde Peeters. Their work appears in journals such as Prenatal Diagnosis, Seminars in Fetal and Neonatal Medicine, European Journal of Human Genetics, European Journal of Medical Genetics and Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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About Paul Brady

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