Soeren S. Lienkamp

Also affiliated with Zurich Insurance Group (Switzerland), ETH Zurich

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome”.

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

Human Mutation(2020)10.1002/humu.24127

N/A

0.464DataRank · unranked

21 citations

Lokuliyange D. S. Senaratne, Elisabeth Ott, Asbjørn Holmgren, Dulika Sumathipala, Selma Mujezinović Larsen +25 more

Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development

Nature Communications(2024)10.1038/s41467-024-53553-2

N/A

0.306DataRank · unranked

6 citations

Munevver Burcu Cicekdal, Richard Holt, Елена А. Сорокина, Nicolas Chassaing, Samuel Clokie +15 more

Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans

Nephrology Dialysis Transplantation(2020)10.1093/ndt/gfaa215

N/A

0.292DataRank · unranked

6 citations

Max Werth, Ana C. Onuchic-Whitford, Maike Getwan, Thomas M. Kitzler, Friedhelm Hildebrandt +15 more

Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2106770118

N/A

0DataRank · unranked

31 citations

Anselm Hoppmann, Pascal Schlosser, Kelli Grand, Weiting Song, R. Diehl +8 more

Deep learning is widely applicable to phenotyping embryonic development and disease

Development(2021)10.1242/dev.199664

N/A

0DataRank · unranked

39 citations

Özgün Çiçek, Paulina Ogar, Max Bürgi, Nikko‐Ideen Shaidani, Michael M. Kaminski +14 more

CRISPR/Cas9 targeting Ttc30a mimics ciliary chondrodysplasia with polycystic kidney disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.27.400994

N/A

0DataRank · unranked

0 citations

Anselm Hoppmann, Pascal Schlosser, Kelli Grand, Weiting Song, R. Diehl +8 more

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

Journal of the American Society of Nephrology(2022)10.1681/asn.2022010050

N/A

0DataRank · unranked

8 citations

Friedhelm Hildebrandt, Chunyan Wang, Thomas Naert, Karin Richter, Theresa Nauth +28 more

SCD5 Regulation by VHL Affects Cell Proliferation and Lipid Homeostasis in ccRCC

Cells(2023)10.3390/cells12060835

N/A

0DataRank · unranked

7 citations

Antonia Philipp, Simon Lagies, Laura Wingendorf, Lu Wang, Felicitas Pilz +9 more

Specific disruption of calcineurin-signaling in the distal convoluted tubule impacts the transcriptome and proteome, and causes hypomagnesemia and metabolic acidosis

Kidney International(2021)10.1016/j.kint.2021.06.030

N/A

0DataRank · unranked

25 citations

Viktória Fisi, Sandra Moser, Agnieszka Wengi, Monique Carrel, Dominique Loffing‐Cueni +8 more