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Franziska Paul
Franziska Paul
Verified email at weizmann.ac.il
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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
18892014
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
11262015
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
5422016
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
4632017
Stats: data and models
RD De Veaux, PF Velleman, DE Bock, AM Vukov, ACM Wong, C Burkett
Pearson/Addison Wesley, 2005
4122005
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
2972017
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
2952018
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
2032019
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
852020
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
782022
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
492018
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
342021
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
332017
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
312014
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
192020
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
122021
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
32019
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
12022
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
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