Ann Swillen

Also affiliated with Center for Human Genetics, KU Leuven

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 15 papers. Top paper: “Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion”.

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

N/A

0.738DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology

Translational Psychiatry(2020)10.1038/s41398-020-0736-7

N/A

0.614DataRank · unranked

59 citations

Samuel J. R. A. Chawner, Thérèse van Amelsvoort, Ann Swillen, Claudia Vingerhoets, Elfi Vergaelen +5 more

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

UNC Libraries(2020)10.17615/86qc-4989

N/A

0DataRank · unranked

0 citations

Thomas Werge, Anders Vangkilde, Koenraad Devriendt, Carolyn Chow, Carrie E. Bearden +27 more

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome

Genes(2022)10.3390/genes13101800

N/A

0DataRank · unranked

4 citations

T. Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H. Zackai +7 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111

N/A

0DataRank · unranked

0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age

American Journal of Obstetrics and Gynecology(2023)10.1016/j.ajog.2023.09.005

N/A

0DataRank · unranked

15 citations

Stephanie Galloway, T. Blaine Crowley, Julie S. Moldenhauer, Ann Swillen, Jeroen Breckpot +57 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y

N/A

0DataRank · unranked

12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more

Gathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research

Genes(2023)10.3390/genes14010169

N/A

0DataRank · unranked

5 citations

T. Blaine Crowley, Brenda Finucane, Emily McClellan, Sarah Donoghue, Sixto García‐Miñáur +10 more

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Molecular Psychiatry(2023)10.1038/s41380-023-02009-y

N/A

0DataRank · unranked

5 citations

Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen +15 more

Endocrine manifestations in adults with 22q11.2 deletion syndrome: a retrospective single-center cohort study

Journal of Endocrinological Investigation(2024)10.1007/s40618-023-02276-0

N/A

0DataRank · unranked

5 citations

Karel David, Ann Swillen, Elfi Vergaelen, M. Docx Op de Beeck, Maarten Hulsmans +3 more

Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter Study

Movement Disorders Clinical Practice(2025)10.1002/mdc3.14354

N/A

0DataRank · unranked

3 citations

Ann Swillen, Gabriela M. Repetto, Nikolai Gil D. Reyes, Anthony E. Lang, Connie Marras +9 more

Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversion

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.04.662981

N/A

0DataRank · unranked

2 citations

DongAhn Yoo, Philip C. Dishuck, Nidhi Koundinya, Erika Souche, William T. Harvey +15 more

Prevalence and spectrum of congenital heart disease in individuals with distal chromosome 22q11.22-23 deletions

medRxiv(2025)10.1101/2025.10.15.25337915

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics(2025)10.1111/cge.70118

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more

Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndrome

Research Square(2025)10.21203/rs.3.rs-8286229/v1

N/A

0DataRank · unranked

0 citations

Valentina Mancini, Marija Dvojakovska, Leila Kushan, Fatouma Mchangama, Feryal Tairi +21 more