Katrien Stouffs

2.1k citations

47 papers · 1.0k indexed · h-index 21

Impact in

Reproductive Medicine top 1%
- Sperm and Testicular Function
Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction

Papers in

Reproductive Medicine 16
- Sperm and Testicular Function 14
Genetics 31
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 19
- Genomics and Rare Diseases 5
- Genetic and Kidney Cyst Diseases 4
- Animal Genetics and Reproduction 4

Co-authors: Willy Lissens Herman Tournaye Inge Liebaers André Van Steirteghem Sara Seneca I. Liebaers Patrick Haentjens Alexander Gheldof
Journals: European Journal of Human Genetics (3 papers)Molecular Human Reproduction (3 papers)Human Reproduction (3 papers)European Journal of Medical Genetics (2 papers)Journal of Assisted Reproduction and Genetics (2 papers)
Partner nations: Belgium Netherlands United States

In The Last Decade

Katrien Stouffs

46 papers receiving 983 citations

Peers

Countries citing papers authored by Katrien Stouffs

Since Specialization

Citations

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

Fields of papers citing papers by Katrien Stouffs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katrien Stouffs. 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 Katrien Stouffs. The network helps show where Katrien Stouffs may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Katrien Stouffs, 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 Katrien Stouffs Line = papers co-authored together Katrien Stouffs links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweight Nature Communications ·F. Cordoliani, Florence Belva, Aafke P.A. van Montfoort, Zebib Haftom, Filippo Zambelli, Sara Seneca, G Reimer, M Bonduelle, Herman Tournaye, Katrien Stouffs, Kurt Barbé, Hubert J.M. Smeets, H. Van de Velde, Karen Sermon, Christophe Blockeel, Claudia Spits	2024	8
2	Loss, Gain and Altered Function of GlyR α2 Subunit Mutations in Neurodevelopmental Disorders Frontiers in Molecular Neuroscience ·Xiumin Chen, Katie A. Wilson, Natascha Schaefer, Xinyi Yao, Mark Windsor, Emmanuel Scalais, Ahn Soyeong, Katrien Stouffs, Carmen Villmann, Megan L. O’Mara, Joseph W. Lynch, Victoria L. Harvey	2022	11
3	Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly Frontiers in Genetics ·Katrien Stouffs, Patrick Verloo, Antonius Kreft, Luc Régal, Diane Beysen, Berten Ceulemans, Anna Jansen, Marije Meuwissen	2020	11
4	Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1 European Journal of Human Genetics ·Antonius Kreft, Katrien Stouffs, Emmanuel Scalais, Marc D’Hooghe, Kathelijn Keymolen, Renzo Guerrini, William B. Dobyns, Nataliya Di Donato, Anna Jansen	2018	25
5	Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations European Journal of Medical Genetics ·Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, PA ARRUDA MELLO, Alice Dica, Daniele Roncati, Kathelijn Keymolen, Sara Seneca, Alexander Gheldof, Linda De Meırleır, Anna Jansen	2018	8
6	A new mutation in the calcium-sensing receptor gene causing hypocalcaemia: case report of a father and two sons. PubMed ·Alba Marina Carranza Valle, Bert Bravenboer, Sara Seneca, Katrien Stouffs, Brigitte Velkeniers	2017	4
7	Detailed molecular characterization of a novel IDS exonic mutation associated with multiple pseudoexon activation Journal of Molecular Medicine ·Lucie Grodecká, Lauren Hedden, 江振伟, Sara Seneca, Katrien Stouffs, Corinne De Laet, С. А. Шавнин, L. Gregory Pawlson, Rihana Sajad, K. Joergensen, Přemysl Souček, Willy Lissens, Emanuele Buratti, Tomáš Freiberger	2016	5
8	Sertoli Cell-Only Syndrome: Behind the Genetic Scenes BioMed Research International ·Katrien Stouffs, Alexander Gheldof, Herman Tournaye, Larisa Yagenich, M Bonduelle, Willy Lissens, Sara Seneca	2016	25
9	Genetic causes of male infertility Annales d Endocrinologie ·Katrien Stouffs, Sara Seneca, Willy Lissens	2014	26
10	A Bumpy Ride on the Diagnostic Bench of Massive Parallel Sequencing, the Case of the Mitochondrial Genome PLoS ONE ·Ingeborg Blaha, Bradford J Matthews, Claudia Spits, Katrien Stouffs, An I. Jonckheere, Linda De Meırleır, Willy Lissens, Arnaud Vanlander, Joél Smet, Boél De Paepe, Rudy Van Coster, Sara Seneca	2014	13
11	Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench? European Journal of Human Genetics ·Sara Seneca, Ingeborg Blaha, Rudy Van Coster, Joél Smet, Willy Lissens, Arnaud Vanlander, Boél De Paepe, An I. Jonckheere, Katrien Stouffs, Linda De Meırleır	2014	31
12	Array comparative genomic hybridization in male infertility Human Reproduction ·Katrien Stouffs, Larisa Yagenich, Remco de Winter, Björn Menten, Sarah Vergult, Herman Tournaye, Willy Lissens	2012	33
13	X chromosomal mutations and spermatogenic failure Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Katrien Stouffs, Willy Lissens	2012	22
14	Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages Reproductive BioMedicine Online ·Katrien Stouffs, Larisa Yagenich, Herman Tournaye, I. Liebaers, Willy Lissens	2010	30
15	Do we need to search for gr/gr deletions in infertile men in a clinical setting? Human Reproduction ·Katrien Stouffs, Herman Tournaye, Josiane Van Der Elst, Patrick Haentjens, I. Liebaers, Willy Lissens	2008	29
16	Alterations of the USP26 gene in Caucasian men International Journal of Andrology ·Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers	2006	29
17	SYCP3 mutations are uncommon in patients with azoospermia Fertility and Sterility ·Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers	2005	31
18	The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletion Human Reproduction ·Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers	2005	52
19	Possible role of USP26 in patients with severely impaired spermatogenesis European Journal of Human Genetics ·Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers	2004	76
20	Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4) Molecular Human Reproduction ·Katrien Stouffs, Willy Lissens, L. Van Landuyt, Herman Tournaye, André Van Steirteghem, Inge Liebaers	2001	18

About Katrien Stouffs

Katrien Stouffs is a scholar working on Reproductive Medicine, Genetics, Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 47 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (19 papers), Sperm and Testicular Function (14 papers), Sexual Differentiation and Disorders (11 papers), Genomics and Rare Diseases (5 papers), Reproductive Biology and Fertility (4 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genetic and Kidney Cyst Diseases (4 papers) and Animal Genetics and Reproduction (4 papers). The work is most often cited by research in Reproductive Medicine (534 citations), Genetics (649 citations), Molecular Biology (618 citations), Public Health, Environmental and Occupational Health (187 citations) and Pediatrics, Perinatology and Child Health (109 citations). Katrien Stouffs has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Willy Lissens, Herman Tournaye, Inge Liebaers, André Van Steirteghem, Sara Seneca, I. Liebaers, Patrick Haentjens, Alexander Gheldof, Anna Jansen and Josiane Van Der Elst. Their work appears in journals such as European Journal of Human Genetics, Molecular Human Reproduction, Human Reproduction, European Journal of Medical Genetics and Journal of Assisted Reproduction and 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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