Brigitte H. W. Faas

3.9k citations

41 papers · 1.8k indexed · h-index 21

Pediatrics, Perinatology and Child Health top 0.5%
Genetics top 5%
Infectious Diseases top 5%
Molecular Biology
Surgery

Co-authors: Lean Beulen Ad Geurts van Kessel Ilse Feenstra Mireille N. Bekker Anthony Odibo Elles M. J. Boon Peter C. J. I. Schielen Irene M. Janssen
Topics: Prenatal Screening and Diagnostics (35 papers)Fetal and Pediatric Neurological Disorders (21 papers)Genomic variations and chromosomal abnormalities (18 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Infectious Diseases
Journals: Clinical Chemistry Molecular Psychiatry Journal of Medical Genetics
Partner nations: Netherlands United States Spain

In The Last Decade

Brigitte H. W. Faas

39 papers receiving 1.7k citations

Peers

Countries citing papers authored by Brigitte H. W. Faas

Since Specialization

Citations

This map shows the geographic impact of Brigitte H. W. Faas'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 Brigitte H. W. Faas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brigitte H. W. Faas more than expected).

Fields of papers citing papers by Brigitte H. W. Faas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brigitte H. W. Faas. 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 Brigitte H. W. Faas. The network helps show where Brigitte H. W. Faas may publish in the future.

Co-authorship network of co-authors of Brigitte H. W. Faas

This figure shows the co-authorship network connecting the top 25 collaborators of Brigitte H. W. Faas. A scholar is included among the top collaborators of Brigitte H. W. Faas based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Brigitte H. W. Faas. Brigitte H. W. Faas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16B 2025 ·American Journal of Medical Genetics Part A ·Servi J.C. Stevens,(unknown),Nicole Y. Souren,Merryn Macville,(unknown),Brigitte H. W. Faas,Bart de Koning,Arthur van den Wijngaard,Sonja de Munnik,Masoud Zamani Esteki	0
2	Detection of human cytomegalovirus cell‐free DNA in pregnant women with symptomatically infected fetuses: proof‐of‐concept study 2025 ·Ultrasound in Obstetrics and Gynecology ·Brigitte H. W. Faas,(unknown),Galuh Astuti,A. Reuss,Kim Stol,Erik A. Sistermans,(unknown),Esther van Leeuwen,Janette Rahamat–Langendoen,Freke A. Wilmink	3
3	Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience 2024 ·Andrology ·Manon S. Oud,(unknown),Dominique Smeets,Liliana Ramos,Godfried W. van der Heijden,(unknown),Maartje van de Vorst,Tom Hofste,Marlies Kempers,Marijn F. Stokman,Kathleen D’Hauwers,Brigitte H. W. Faas,Dineke Westra	2
4	Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testing 2024 ·EBioMedicine ·Brigitte H. W. Faas,Galuh Astuti,Willem J. G. Melchers,A. Reuss,Christian Gilissen,Merryn Macville,(unknown),(unknown),Malgorzata I. Srebniak,(unknown),Janette Rahamat–Langendoen,Erik A. Sistermans,(unknown)	10
5	Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype 2019 ·Human Genetics ·Przemysław Szafrański,Qian Liu,Justyna A. Karolak,Xiaofei Song,Nicole de Leeuw,Brigitte H. W. Faas,(unknown),Petr Janků,Marta Ježová,(unknown),Kathleen Gibbs,Lea F. Surrey,(unknown),Denis Bérubé,Luc L. Oligny,Jacques L. Michaud,Edwina J. Popek,Paweł Stankiewicz	16
6	Women's Experience with Non‐Invasive Prenatal Testing and Emotional Well‐being and Satisfaction after Test‐Results 2017 ·Journal of Genetic Counseling ·Rachèl V. van Schendel,Godelieve C.M.L. Page‐Christiaens,Lean Beulen,Caterina M. Bilardo,Marjon A. de Boer,A. Coumans,Brigitte H. W. Faas,Irene M. van Langen,Klaske D. Lichtenbelt,Merel C. van Maarle,Merryn Macville,Dick Oepkes,Eva Pajkrt,Lidewij Henneman	37
7	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part I—clinical impact 2016 ·Prenatal Diagnosis ·Dick Oepkes,Godelieve C.M.L. Page‐Christiaens,Caroline J. Bax,Mireille N. Bekker,Catia M. Bilardo,Elles M. J. Boon,G. Heleen Schuring‐Blom,A. Coumans,Brigitte H. W. Faas,Robert‐Jan H. Galjaard,Attie T. J. I. Go,Lidewij Henneman,Merryn Macville,Eva Pajkrt,Ron F. Suijkerbuijk,Karin Huijsdens–van Amsterdam,Diane Van Opstal,E. J. T. Verweij,Marjan M. Weiss,Erik A. Sistermans	110
8	Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part II—women's perspectives 2016 ·Prenatal Diagnosis ·Rachèl V. van Schendel,Godelieve C.M.L. Page‐Christiaens,Lean Beulen,Catia M. Bilardo,Marjon A. de Boer,A. Coumans,Brigitte H. W. Faas,Irene M. van Langen,Klaske D. Lichtenbelt,Merel C. van Maarle,Merryn Macville,Dick Oepkes,Eva Pajkrt,Lidewij Henneman	55
9	P01.07: The clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies 2016 ·Ultrasound in Obstetrics and Gynecology ·Lean Beulen,Brigitte H. W. Faas,Ilse Feenstra,(unknown),Mireille N. Bekker	1
10	Prenatal genetic care: debates and considerations of the past, present and future 2015 ·Expert Opinion on Biological Therapy ·Brigitte H. W. Faas	6
11	The consequences of implementing non-invasive prenatal testing in Dutch national health care: a cost-effectiveness analysis 2014 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Lean Beulen,Janneke P.C. Grutters,Brigitte H. W. Faas,Ilse Feenstra,J. M. G. van Vugt,Mireille N. Bekker	47
12	Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories 2014 ·Expert Review of Molecular Diagnostics ·Djie Tjwan Thung,Lean Beulen,Jayne Y. Hehir‐Kwa,Brigitte H. W. Faas	15
13	Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings 2013 ·European Journal of Human Genetics ·(unknown),Willy M. Nillesen,Kyra E. Stuurman,Grétel Oudesluijs,(unknown),(unknown),Charlotte W. Ockeloen,Inge B. Mathijssen,Marga Schepens,Martina Ruiterkamp‐Versteeg,Hans Scheffer,Brigitte H. W. Faas,Ineke van der Burgt,Helger G. Yntema	93
14	Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24 h after venipuncture 2013 ·Clinical Biochemistry ·Karen Buysse,Lean Beulen,(unknown),Christian Gilissen,(unknown),Irene M. Janssen,(unknown),Joep de Ligt,Ilse Feenstra,Mireille N. Bekker,J. M. G. van Vugt,Ad Geurts van Kessel,Lisenka E.L.M. Vissers,Brigitte H. W. Faas	14
15	Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies 2013 ·Prenatal Diagnosis ·Elles M. J. Boon,Brigitte H. W. Faas	44
16	Is routine karyotyping required in prenatal samples with a molecular or metabolic referral? 2012 ·Molecular Cytogenetics ·Angelique J. A. Kooper,(unknown),Brigitte H. W. Faas,Lies H. Hoefsloot,Ineke van der Burgt,H.A. Zondervan,Arie P.T. Smits	2
17	Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells 2012 ·Expert Opinion on Biological Therapy ·Brigitte H. W. Faas,Joep de Ligt,Irene M. Janssen,Alex J. Eggink,Lia D. E. Wijnberger,(unknown),Lisenka E.L.M. Vissers,Ad Geurts van Kessel	104
18	Increased cerebrospinal fluid chitotriosidase index in patients with multiple sclerosis 2009 ·Acta Neurologica Scandinavica ·Marcel M. Verbeek,(unknown),Brigitte H. W. Faas,(unknown),Peter Joseph Jongen	17
19	CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy 2007 ·Molecular Psychiatry ·Joseph I. Friedman,Terry Vrijenhoek,Sander Markx,Irene M. Janssen,(unknown),Brigitte H. W. Faas,Nine V.A.M. Knoers,Wiepke Cahn,René S. Kahn,Lisa Edelmann,Keith L. Davis,Jeremy M. Silverman,Han G. Brunner,Ad Geurts van Kessel,Cisca Wijmenga,Roel A. Ophoff,Joris A. Veltman	224
20	Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defects 2006 ·Prenatal Diagnosis ·Angelique J. A. Kooper,Dagmar de Bruijn,(unknown),Brigitte H. W. Faas,(unknown),Chris M.G. Thomas,Arie P.T. Smits	21

About Brigitte H. W. Faas

Brigitte H. W. Faas is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases, having authored 41 papers that have together received 1.8k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (35 papers), Fetal and Pediatric Neurological Disorders (21 papers) and Genomic variations and chromosomal abnormalities (18 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.2k citations), Genetics (674 citations) and Infectious Diseases (411 citations). Brigitte H. W. Faas has collaborated with scholars based in Netherlands, United States and Spain. Frequent co-authors include Lean Beulen, Ad Geurts van Kessel, Ilse Feenstra, Mireille N. Bekker, Anthony Odibo, Elles M. J. Boon, Peter C. J. I. Schielen, Irene M. Janssen, Rossa W. K. Chiu and Nicole de Leeuw. Their work appears in journals such as Clinical Chemistry, Molecular Psychiatry and Journal of Medical Genetics.

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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