Erik Boot

Also affiliated with Maastricht University, 's Heeren Loo

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 8 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

Possible underreporting of pathogenic variants in RAI1 causing Smith–Magenis syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62380

N/A

0DataRank · unranked

18 citations

Cathelijne C. Linders, Sterre H. Tromp, Marie‐José H. van den Boogaard, Agnies M. van Eeghen, Erik Boot

Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation

Prenatal Diagnosis(2024)10.1002/pd.6566

N/A

0DataRank · unranked

7 citations

Anne S. Bassett, Erik Boot, Bruno Marino, Julie S. Moldenhauer, Sólveig Óskarsdóttir +6 more

Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion

International Journal of Obesity(2024)10.1038/s41366-024-01685-2

N/A

0DataRank · unranked

3 citations

Emma N. M. M. von Scheibler, Elisabeth F. C. van Rossum, Mieke M. van Haelst, Claudia Vingerhoets, Thérèse van Amelsvoort +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

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