Uwe Kornak

Also affiliated with Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Max Planck Institute for Molecular Genetics, University of Göttingen, Charité - Universitätsmedizin Berlin

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 7 papers. Top paper: “Issue Information”.

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

Efficient generation of osteoclasts from human induced pluripotent stem cells and functional investigations of lethal CLCN7-related osteopetrosis

Journal of Bone and Mineral Research(2020)10.1002/jbmr.4322

N/A

0DataRank · unranked

53 citations

Anna Floriane Hennig, Nina Stelzer, Shroddha Bose, Johannes Kopp, Kent Søe +13 more

Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism

Bone(2020)10.1016/j.bone.2019.115219

N/A

0DataRank · unranked

19 citations

Kristina Cusmano‐Ozog, Rainer Koenig, Manuel Holtgrewe, Banu Nur, Ercan Mıhçı +16 more

Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis

Genetics in Medicine(2022)10.1016/j.gim.2022.07.012

N/A

0DataRank · unranked

4 citations

Özgür Çoğulu, Davut Pehli̇van, Saranya Balachandran, Pedro Vallecillo-García, Christopher M. Grochowski +19 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

0DataRank · unranked

5 citations

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

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

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

N/A

0DataRank · unranked

36 citations

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

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Nature Genetics(2024)10.1038/s41588-024-01836-1

N/A

0DataRank · unranked

49 citations

Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Tzung‐Chien Hsieh +95 more