International Journal of Mass Spectrometry

Papers
(The H4-Index of International Journal of Mass Spectrometry is 16. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)
ArticleCitations
Improved in situ zircon U–Pb dating at high spatial resolution (5–16 μm) by laser ablation–single collector–sector field–ICP–MS using Jet sample and X skimmer cones33
Structural elucidation of phosphatidylcholines from tissue using electron induced dissociation32
Using Orbitrap mass spectrometry to assess the isotopic compositions of individual compounds in mixtures29
Exploring frontiers of orbitrap performance for long transients29
Emerging microdroplet chemistry for synthesis and analysis26
Pushing the limits of native MS: Online SEC-native MS for structural biology applications24
Investigating native capillary zone electrophoresis-mass spectrometry on a high-end quadrupole-time-of-flight mass spectrometer for the characterization of monoclonal antibodies24
Laser Desorption Mass Spectrometry at Saturn’s moon Titan23
Vibrational spectroscopy of the cryogenically cooled O- and N-protomers of 4-aminobenzoic acid: Tag effects, isotopic labels, and identification of the E,Z isomer of the O-protomer22
Ambient ionisation mass spectrometry for the trace detection of explosives using a portable mass spectrometer22
Fragmentation pathways of odd- and even-electron N-alkylated synthetic cathinones19
An improved peak detection algorithm in mass spectra combining wavelet transform and image segmentation18
Contemporary ion mobility spectrometry applications and future trends towards environmental, health and food research: A review18
Identification and quantification of cytotoxic phenolic acids and flavonoids in Ixora brachiata by UHPLC-DAD and UHPLC-ESI-MS/MS17
Protonation isomers of highly charged protein ions can be separated in FAIMS-MS16
Fragmentation pathways of α-pyrrolidinophenone synthetic cathinones and their application to the identification of emerging synthetic cathinone derivatives16
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