Koenraad Devriendt

Also affiliated with Center for Human Genetics, Catholic University of America, KU Leuven

Biochemistry, Genetics and Molecular BiologyMedicine

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 14 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

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.014

N/A

0.546DataRank · unranked

37 citations

Vanda McNiven, Cheryl Cytrynbaum, Maryam Jangjoo, Margaret P Adam, Hans T. Björnsson +57 more

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature

European Journal of Human Genetics(2020)10.1038/s41431-020-0571-6

N/A

0DataRank · unranked

38 citations

Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, Julien Thévenon, Ange‐Line Bruel +60 more

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome

Clinical Genetics(2020)10.1111/cge.13878

N/A

0DataRank · unranked

26 citations

Samuel Nicaise, Manuela Antin, Anne‐Sophie Leuvrey, Elsa Nourisson, Carmen C. Leitch +22 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

Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

Carolina Digital Repository (University of North Carolina at Chapel Hill)(2020)10.17615/x8dg-7b55

N/A

0DataRank · unranked

0 citations

Alan Fryer, Koenraad Devriendt, Richard H. Scott, Jules G. Leroy, Ingrid P.C. Krapels +27 more

Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population‐specific measurements

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62958

N/A

0DataRank · unranked

3 citations

Mathieu Roelants, Aimé Lumaka, Prince Makay, Dahlie Tshika, Toni Kasole Lubala +3 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

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.01.013

N/A

0DataRank · unranked

25 citations

Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene +95 more

Greig cephalopolysyndactyly contiguous gene syndrome in a Congolese patient co-occurring with sickle cell anemia, and review of literature

Clinical Dysmorphology(2024)10.1097/mcd.0000000000000510

N/A

0DataRank · unranked

0 citations

Corinne Fasquelle, Gerrye Mubungu, Esther Ekolo, Aimée Mupuala, Patrick Fuanani +9 more

Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions

European Journal of Human Genetics(2025)10.1038/s41431-025-01916-8

N/A

0DataRank · unranked

2 citations

Xiaonan Zhao, Nichole Owen, Tom Evans, Muriel Holder‐Espinasse, Nayana Lahiri +28 more

A training program to extend the reach of the deciphering developmental disorders in Africa (DDD-Africa) study

Frontiers in Genetics(2025)10.3389/fgene.2025.1611047

N/A

0DataRank · unranked

0 citations

Zané Lombard, Nadia Carstens, Zandisiwe Goliath, Aimé Lumaka, Prince Makay +6 more

Closing the diagnostic gap in developmental disorders through comprehensive long-read sequencing

10.21203/rs.3.rs-9108777/v1

N/A

0DataRank · unranked

0 citations

Mathilde Geysens, Benjamin Huremagic, Erika Souche, Greet Peeters, Natalia Olszewska +12 more

De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.015

N/A

0DataRank · unranked

43 citations

Tonya Moss, Hannah W. Moore, Koenraad Devriendt, Heather Flanagan‐Steet, Melanie May +15 more