Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state S Smajić, CA Prada-Medina, Z Landoulsi, J Ghelfi, S Delcambre, ... Brain 145 (3), 964-978, 2022 | 238 | 2022 |
The histone methyltransferase DOT1L is required for proper DNA damage response, DNA repair, and modulates chemotherapy responsiveness V Kari, SK Raul, JM Henck, J Kitz, F Kramer, RL Kosinsky, N Übelmesser, ... Clinical epigenetics 11 (1), 1-13, 2019 | 51 | 2019 |
Single-cell sequencing of the human midbrain reveals glial activation and a neuronal state specific to Parkinson's disease S Smajic, CA Prada-Medina, Z Landoulsi, C Dietrich, J Jarazo, J Henck, ... medRxiv (The Preprint Server for health sciences.), 2020 | 19 | 2020 |
Single-cell RNA-based phenotyping reveals a pivotal role of thyroid hormone receptor alpha for hypothalamic development VKA Sreenivasan, R Dore, J Resch, J Maier, C Dietrich, J Henck, ... Development 150 (3), dev201228, 2023 | 7 | 2023 |
Single-cell, whole-embryo phenotyping of mammalian developmental disorders X Huang, J Henck, C Qiu, VKA Sreenivasan, S Balachandran, OV Amarie, ... Nature 623 (7988), 772-781, 2023 | 6 | 2023 |
Single cell, whole embryo phenotyping of pleiotropic disorders of mammalian development X Huang, J Henck, C Qiu, VKA Sreenivasan, S Balachandran, R Behncke, ... bioRxiv, 2022.08. 03.500325, 2022 | 4 | 2022 |
Single-cell sequencing: promises and challenges for human genetics VKA Sreenivasan, J Henck, M Spielmann Medizinische Genetik 34 (4), 261-273, 2022 | 1 | 2022 |
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult‐Onset Demyelinating Leukodystrophy P Dimartino, M Zadorozhna, V Yumiceba, A Basile, I Cani, US Melo, ... Annals of neurology, 2024 | | 2024 |
Single-cell RNA phenotyping of a mouse model for hypothyroidism reveals a pivotal role of thyroid hormone receptor alpha for hypothalamic development V Sreenivasan, R Dore, J Resch, J Maier, C Dietrich, J Henck, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 622-622, 2024 | | 2024 |
Single cell, whole embryo phenotyping of pleiotropic disorders of mammalian development J Henck, X Huang, C Qiu, V Sreenivasan, S Ulferts, R Behncke, ... | | 2023 |
Single cell sequencing as a phenotyping strategy to decipher the molecular mechanisms of developmental disorders J Henck | | 2023 |
Single-cell characterization of patient midbrain tissue reveals tissue remodeling and glial activation in Parkinson's disease S Smajic, C Prada-Medina, Z Landoulsi, J Ghelfi, S Delcambre, C Dietrich, ... MOVEMENT DISORDERS 37, S595-S595, 2022 | | 2022 |
Transcriptional single-cell atlas of human limb malformation candidate genes CA Prada-Medina, G Cova, J Glaser, C Dietrich, J Henck, S Mundlos, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 133-133, 2020 | | 2020 |
The Cdkl5 phenotype at single cell resolution J Henck, C Prada, Y Herault, C Dietrich, V Suckow, VM Kalscheuer, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 381-381, 2020 | | 2020 |
The histone methyltransferase DOT1L is required for proper DNA damage response, DNA repair, and modulates chemotherapy responsiveness K Vijayalakshmi, SK Raul, JM Henck, J Kitz, F Kramer, RL Kosinsky, ... Clinical Epigenetics 11, 2019 | | 2019 |