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Brain : a Journal of Neurology|December 23, 2023
Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental diseaseRalf A Husain, Xinfu Jiao, J Christopher Hennings, et al.
Physical Review Letters|December 27, 2015
New Short-Lived Isotope ^{221}U and the Mass Surface Near N=126J Khuyagbaatar, A Yakushev, Ch E Düllmann, et al.
Physical Review Letters|September 28, 2010
Production and decay of element 114: high cross sections and the new nucleus 277HsCh E Düllmann, M Schädel, A Yakushev, et al.
Frontiers in Chemistry|December 17, 2021
First Study on Nihonium (Nh, Element 113) Chemistry at TASCAA Yakushev, L Lens, Ch E Düllmann, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
Frontiers in Chemistry|September 12, 2022
On the adsorption and reactivity of element 114, fleroviumA Yakushev, L Lens, Ch E Düllmann, et al.
Physical Review Letters|May 20, 2014
48Ca+249Bk fusion reaction leading to element Z = 117: long-lived α-decaying 270Db and discovery of 266LrJ Khuyagbaatar, A Yakushev, Ch E Düllmann, et al.
Brain : a Journal of Neurology|September 28, 2023
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.
Nature Genetics|July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosisWouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
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