Aija Kyttälä

2.2k citations

25 papers · 1.6k indexed · h-index 22

Co-authors: Anu Jalanko Leena Peltonen Anu Suomalainen Valeria Tiranti Giacomo P. Comi Massimo Zeviani Sirkka Keränen Jyrki Kaukonen
Topics: Lysosomal Storage Disorders Research (18 papers)Cellular transport and secretion (15 papers)Calcium signaling and nucleotide metabolism (7 papers)
Cited by: Physiology Clinical Biochemistry Cell Biology
Journals: Science Journal of Biological Chemistry Journal of Neuroscience
Partner nations: Finland United States United Kingdom

In The Last Decade

Aija Kyttälä

25 papers receiving 1.6k citations

Peers

Countries citing papers authored by Aija Kyttälä

Since Specialization

Citations

This map shows the geographic impact of Aija Kyttälä's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Aija Kyttälä with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aija Kyttälä more than expected).

Fields of papers citing papers by Aija Kyttälä

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aija Kyttälä. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Aija Kyttälä. The network helps show where Aija Kyttälä may publish in the future.

Co-authorship network of co-authors of Aija Kyttälä

This figure shows the co-authorship network connecting the top 25 collaborators of Aija Kyttälä. A scholar is included among the top collaborators of Aija Kyttälä based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aija Kyttälä. Aija Kyttälä is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells 2022 ·Stem Cell Reports ·(unknown),Masahito Yoshihara,Jouni Kvist,(unknown),Warren Andrew,(unknown),Eeva‐Mari Jouhilahti,Helena Kilpinen,Diego Balboa,Shintaro Katayama,Aija Kyttälä,Juha Kere,Timo Otonkoski,Jere Weltner,Ras Trokovic	25
2	Multiparametric platform for profiling lipid trafficking in human leukocytes 2022 ·Cell Reports Methods ·Simon G. Pfisterer,(unknown),Kristiina Kanerva,(unknown),Lassi Paavolainen,Pietari Ripatti,(unknown),Aija Kyttälä,Maria Donata Di Taranto,(unknown),Giuliana Fortunato,Johanna Kuusisto,Péter Horváth,Samuli Ripatti,Markku Laakso,Elina Ikonen	5
3	Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma 2019 ·BMC Cancer ·Erlend Skaga,Evgeny Kulesskiy,(unknown),Cecilie Sandberg,Swapnil Potdar,Aija Kyttälä,Iver A. Langmoen,Aki Laakso,Emília Gaál‐Paavola,Markus Perola,Krister Wennerberg,Einar Osland Vik-Mo	55
4	Genetic Variability Overrides the Impact of Parental Cell Type and Determines iPSC Differentiation Potential 2016 ·Stem Cell Reports ·Aija Kyttälä,Roksana Moraghebi,Cristina Valensisi,Johannes Kettunen,Colin Andrus,(unknown),Mahito Nakanishi,Ken Nishimura,Manami Ohtaka,Jere Weltner,Ben Van Handel,Olavi Parkkonen,Juha Sinisalo,Anu Jalanko,R. David Hawkins,Niels-Bjarne Woods,Timo Otonkoski,Ras Trokovic	176
5	Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutations 2014 ·Journal of Neurology ·Cecilia Mancini,(unknown),Yiran Guo,Yulan Chen,Elisa Giorgio,Alessandro Brussino,Eleonora Di Gregorio,Simona Cavalieri,Nicola Lo Buono,Ada Funaro,(unknown),Bruce Nmezi,Aija Kyttälä,Filippo M. Santorelli,(unknown),Håkon Håkonarson,Hao Zhang,Alfredo Brusco	30
6	Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments 2012 ·Cellular and Molecular Life Sciences ·Kristiina Uusi-Rauva,Aija Kyttälä,Rik van der Kant,Jouni Vesa,Kimmo Tanhuanpää,Jacques Neefjes,Vesa M. Olkkonen,Anu Jalanko	63
7	The neuronal ceroid lipofuscinosis protein CLN5: new insights into cellular maturation, transport, and consequences of mutations 2010 ·Human Mutation ·(unknown),Carlos Bessa,Claudia Heine,G. Ribeiro,Anu Jalanko,Aija Kyttälä	39
8	Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis 2010 ·Human Molecular Genetics ·(unknown),Maria Kousi,Corinne Sagné,Gian Carlo Bellenchi,Lydie Morel,Michèle Darmon,Helena Hůlková,Raquel Ruivo,Cécile Debacker,Salah El Mestikawy,M. Elleder,Anna‐Elina Lehesjoki,Anu Jalanko,Bruno Gasnier,Aija Kyttälä	44
9	Novel interactions of CLN5 support molecular networking between Neuronal Ceroid Lipofuscinosis proteins 2009 ·BMC Cell Biology ·Annina Lyly,Carina von Schantz,Claudia Heine,(unknown),Tessa Sipilä,Anu Jalanko,Aija Kyttälä	65
10	Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian Sibship 2009 ·Human Mutation ·(unknown),Stephan Storch,Franz Rüschendorf,(unknown),Aija Kyttälä,Sara Mole,Claudia Kitzmüller,Kathrin Saar,Leena Mewasingh,(unknown),Alfried Kohlschütter,Kurt Ullrich,Thomas Braulke,Angela Schulz	43
11	Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism 2008 ·Human Molecular Genetics ·Annina Lyly,Sanna Marjavaara,Aija Kyttälä,Kristiina Uusi-Rauva,Kaisu Luiro,Outi Kopra,Laurent O. Martinez,Kimmo Tanhuanpää,Nisse Kalkkinen,Anu Suomalainen,Matti Jauhiainen,Anu Jalanko	53
12	Novel interactions of CLN3 protein link Batten disease to dysregulation of fodrin–Na+, K+ ATPase complex 2008 ·Experimental Cell Research ·Kristiina Uusi-Rauva,Kaisu Luiro,Kimmo Tanhuanpää,Outi Kopra,Pablo Martı́n-Vasallo,Aija Kyttälä,Anu Jalanko	41
13	Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1) – distinct characteristics in neurons 2007 ·BMC Cell Biology ·Annina Lyly,Carina von Schantz,(unknown),Outi Kopra,Jani Saarela,Matti Jauhiainen,Aija Kyttälä,Anu Jalanko	34
14	Functional biology of the neuronal ceroid lipofuscinoses (NCL) proteins 2006 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Aija Kyttälä,Ulla Lahtinen,Thomas Braulke,Sandra L. Hofmann	73
15	AP-1 and AP-3 Facilitate Lysosomal Targeting of Batten Disease Protein CLN3 via Its Dileucine Motif 2004 ·Journal of Biological Chemistry ·Aija Kyttälä,(unknown),Peter Schu,Anu Jalanko,J. Paul Luzio	50
16	Differential Use of Two AP‐3‐mediated Pathways by Lysosomal Membrane Proteins 2004 ·Traffic ·Gudrun Ihrke,Aija Kyttälä,Matthew R. G. Russell,Brian Rous,J. Paul Luzio	57
17	Two Motifs Target Batten Disease Protein CLN3 to Lysosomes in Transfected Nonneuronal and Neuronal Cells 2003 ·Molecular Biology of the Cell ·Aija Kyttälä,Gudrun Ihrke,Jouni Vesa,Michael J. Schell,J. Paul Luzio	95
18	Expression of Palmitoyl Protein Thioesterase in Neurons 2000 ·Molecular Genetics and Metabolism ·Outi Heinonen,Aija Kyttälä,(unknown),Tiina Paunio,Leena Peltonen,Anu Jalanko	66
19	Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouse 1998 ·Gene Therapy ·Minna Peltola,Aija Kyttälä,O. P. Heinonen,Juhani Rapola,(unknown),Frédéric Revah,Leena Peltonen,Anu Jalanko	31
20	Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and liver of aspartylglucosaminuria (AGU) mouse 1998 ·STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) ·Minna Peltola,Aija Kyttälä,O. P. Heinonen,Juhani Rapola,(unknown),Frédéric Revah,Leena Peltonen,Anu Jalanko	1

About Aija Kyttälä

Aija Kyttälä is a scholar working on Physiology, Cell Biology and Physiology, having authored 25 papers that have together received 1.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (18 papers), Cellular transport and secretion (15 papers) and Calcium signaling and nucleotide metabolism (7 papers). The work is most often cited by research in Physiology (211 citations), Clinical Biochemistry (282 citations) and Cell Biology (513 citations). Aija Kyttälä has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Anu Jalanko, Leena Peltonen, Anu Suomalainen, Valeria Tiranti, Giacomo P. Comi, Massimo Zeviani, Sirkka Keränen, Jyrki Kaukonen, J. Paul Luzio and Gudrun Ihrke. Their work appears in journals such as Science, Journal of Biological Chemistry and Journal of Neuroscience.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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