Massively parallel single-cell RNA-seq for marker-free decomposition of tissues into cell types DA Jaitin, E Kenigsberg, H Keren-Shaul, N Elefant, F Paul, I Zaretsky, ... Science 343 (6172), 776-779, 2014 | 1920 | 2014 |
Transcriptional heterogeneity and lineage commitment in myeloid progenitors F Paul, Y Arkin, A Giladi, DA Jaitin, E Kenigsberg, H Keren-Shaul, ... Cell 163 (7), 1663-1677, 2015 | 1140 | 2015 |
The spectrum and regulatory landscape of intestinal innate lymphoid cells are shaped by the microbiome M Gury-BenAri, CA Thaiss, N Serafini, DR Winter, A Giladi, D Lara-Astiaso, ... Cell 166 (5), 1231-1246. e13, 2016 | 557 | 2016 |
Systemic human ILC precursors provide a substrate for tissue ILC differentiation AI Lim, Y Li, S Lopez-Lastra, R Stadhouders, F Paul, A Casrouge, ... Cell 168 (6), 1086-1100. e10, 2017 | 472 | 2017 |
Stats: data and models RD De Veaux, PF Velleman, DE Bock, AM Vukov, ACM Wong, C Burkett Pearson/Addison Wesley, 2005 | 418 | 2005 |
Single-cell characterization of haematopoietic progenitors and their trajectories in homeostasis and perturbed haematopoiesis A Giladi, F Paul, Y Herzog, Y Lubling, A Weiner, I Yofe, D Jaitin, ... Nature cell biology 20 (7), 836-846, 2018 | 307 | 2018 |
Genomic characterization of murine monocytes reveals C/EBPβ transcription factor dependence of Ly6C− cells A Mildner, J Schönheit, A Giladi, E David, D Lara-Astiaso, ... Immunity 46 (5), 849-862. e7, 2017 | 301 | 2017 |
MARS-seq2. 0: an experimental and analytical pipeline for indexed sorting combined with single-cell RNA sequencing H Keren-Shaul, E Kenigsberg, DA Jaitin, E David, F Paul, A Tanay, I Amit Nature protocols 14 (6), 1841-1862, 2019 | 211 | 2019 |
Cxcl10+ monocytes define a pathogenic subset in the central nervous system during autoimmune neuroinflammation A Giladi, LK Wagner, H Li, D Dörr, C Medaglia, F Paul, A Shemer, S Jung, ... Nature immunology 21 (5), 525-534, 2020 | 91 | 2020 |
MYCN mediates cysteine addiction and sensitizes neuroblastoma to ferroptosis H Alborzinia, AF Flórez, S Kreth, LM Brückner, U Yildiz, M Gartlgruber, ... Nature cancer 3 (4), 471-485, 2022 | 89 | 2022 |
Differences in cell cycle status underlie transcriptional heterogeneity in the HSC compartment FKB Lauridsen, TL Jensen, N Rapin, D Aslan, AS Wilhelmson, S Pundhir, ... Cell reports 24 (3), 766-780, 2018 | 51 | 2018 |
Identical twins carry a persistent epigenetic signature of early genome programming J van Dongen, SD Gordon, AF McRae, VV Odintsova, H Mbarek, ... Nature Communications 12 (1), 5618, 2021 | 38 | 2021 |
MicroRNA‐142 controls thymocyte proliferation A Mildner, E Chapnik, D Varol, T Aychek, N Lampl, N Rivkin, A Bringmann, ... European journal of immunology 47 (7), 1142-1152, 2017 | 37 | 2017 |
Plasticity in the transcriptional and epigenetic circuits regulating dendritic cell lineage specification and function F Paul, I Amit Current Opinion in Immunology 30, 1-8, 2014 | 31 | 2014 |
Bleeding signs due to acquired von Willebrand syndrome at diagnosis of chronic myeloid leukaemia in children R Knoefler, BS Lange, F Paul, O Tiebel, M Suttorp British Journal of Haematology 188 (5), 701-706, 2020 | 19 | 2020 |
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy HH Wong, SH Seet, M Maier, A Gurel, RM Traspas, C Lee, S Zhang, ... The American Journal of Human Genetics 108 (7), 1301-1317, 2021 | 13 | 2021 |
Cxcl10 (+) monocytes define a pathogenic subset in the central nervous system during autoimmune neuroinflammation (vol 21, pg 525, 2020) A Giladi, LK Wagner, H Li, D Doerr, C Medaglia, F Paul, A Shemer, ... NATURE IMMUNOLOGY 21 (8), 962-962, 2020 | 4* | 2020 |
High Platelet counts, thrombosis, bleeding signs, and acquired von willebrand syndrome at diagnosis of pediatric chronic myeloid leukemia M Suttorp, R Knoefler, H Deutsch, F Paul, O Tiebel, M Metzler, F Millot Blood 134, 4152, 2019 | 3 | 2019 |
Inactivation of DRG1, encoding a translation factor GTPase, causes a Recessive Neurodevelopmental Disorder CAE Westrip, F Paul, F Al-Murshedi, H Qaitoon, B Cham, SC Fletcher, ... medRxiv, 2022.09. 20.22279914, 2022 | 2 | 2022 |
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder F Paul, C Ng, UB Mohamad Sahari, S Nafissi, Y Nilipoor, AR Tavasoli, ... Human Molecular Genetics 31 (21), 3729-3740, 2022 | | 2022 |