Vera M. Kalscheuer

Max Planck Institute for Molecular Genetics

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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 9 papers. Top paper: “Single-cell, whole-embryo phenotyping of mammalian developmental disorders”.

Single-cell, whole-embryo phenotyping of mammalian developmental disorders

Nature(2023)10.1038/s41586-023-06548-w

N/A

0.546DataRank · unranked

37 citations

Jana Henck, Chengxiang Qiu, Varun K. A. Sreenivasan, Saranya Balachandran, Oana V. Amarie +36 more

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

medRxiv(2022)10.1101/2022.02.15.22270795

N/A

0.373DataRank · unranked

11 citations

Mana M. Mehrjouy, Ryan L. Collins, Mads Bak, Olga Dudchenko, Harrison Brand +95 more

Single cell, whole embryo phenotyping of pleiotropic disorders of mammalian development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.03.500325

N/A

0.269DataRank · unranked

5 citations

Jana Henck, Chengxiang Qiu, Varun K. A. Sreenivasan, Saranya Balachandran, Rose Yinghan Behncke +28 more

Variants in CUL4B are Associated with Cerebral Malformations

UNC Libraries(2020)10.17615/wkgc-ft42

N/A

0.208DataRank · unranked

3 citations

Krysta Voesenek, Michèl A.A.P. Willemsen, Ewa Obersztyn, Yue Xiong, Bert B.A. de Vries +24 more

A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3′ end processing is associated with intellectual disability in humans

Nucleic Acids Research(2020)10.1093/nar/gkaa689

N/A

0DataRank · unranked

18 citations

Elahe Masoumzadeh, Vera M. Kalscheuer, Thierry Bienvenu, Pierre Billuart, Marie‐Ange Delrue +3 more

Genotype-Phenotype Correlation in RBM10-Associated Syndromes – How Variant Function Shapes a Broad Phenotypic Landscape

medRxiv(2025)10.1101/2025.08.05.25330579

N/A

0DataRank · unranked

0 citations

Christina Fagerberg, Thomas Koed Doktor, Mia M. Rosenlund, Santiago M. Lumbreras, Mark Burton +70 more

Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review

Clinical Genetics(2020)10.1111/cge.13831

N/A

0DataRank · unranked

15 citations

Sara K. Young, Vanessa Suckow, Alexis G. Thornburg, Matias Wagner, Inga Harting +5 more

A Point Mutation in the RNA Recognition Motif of CSTF2 Associated with Intellectual Disability in Humans Causes Defects in 3′ End Processing

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.02.893107

N/A

0DataRank · unranked

0 citations

Elahe Masoumzadeh, Vera M. Kalscheuer, Thierry Bienvenu, Pierre Billuart, Marie-Ange Delrue +3 more

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

Nature Communications(2022)10.1038/s41467-022-34264-y

N/A

0DataRank · unranked

45 citations

Christopher Schröder, Ilaria Parenti, Carine Dalle, Agnès Rastetter, Theresa Kühnel +32 more