Jouni Vesa

3.2k citations

35 papers · 2.5k indexed · 1 hit paper · h-index 21

Co-authors: Virginia Kimonis Leena Peltonen Elina Hellsten Juhani Rapola Pirkko Santavuori Sandra L. Hofmann Linda A. Verkruyse Giles Watts
Topics: Lysosomal Storage Disorders Research (16 papers)Cellular transport and secretion (9 papers)Autophagy in Disease and Therapy (6 papers)
Cited by: Cell Biology Physiology
Journals: Nature Journal of Biological Chemistry PLoS ONE
Partner nations: United States Finland United Kingdom

In The Last Decade

Jouni Vesa

34 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

1995 606 citations Jouni Vesa, Elina Hellsten et al. profile →

Peers

Countries citing papers authored by Jouni Vesa

Since Specialization

Citations

This map shows the geographic impact of Jouni Vesa'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 Jouni Vesa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jouni Vesa more than expected).

Fields of papers citing papers by Jouni Vesa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jouni Vesa. 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 Jouni Vesa. The network helps show where Jouni Vesa may publish in the future.

Co-authorship network of co-authors of Jouni Vesa

This figure shows the co-authorship network connecting the top 25 collaborators of Jouni Vesa. A scholar is included among the top collaborators of Jouni Vesa 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 Jouni Vesa. Jouni Vesa 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	Increased HIV-1 superinfection risk in carriers of specific human leukocyte antigen alleles 2017 ·AIDS ·Jouni Vesa,Antoine Chaillon,Gabriel A. Wagner,Christy M. Anderson,Douglas D. Richman,Davey M. Smith,Susan J. Little	7
2	Data on characterizing the gene expression patterns of neuronal ceroid lipofuscinosis genes: CLN1, CLN2, CLN3, CLN5 and their association to interneuron and neurotransmission markers: Parvalbumin and Somatostatin 2016 ·Data in Brief ·(unknown),Anna‐Liisa Fabritius,Jouni Vesa,Leena Peltonen	6
3	In vitro studies in VCP-associated multisystem proteinopathy suggest altered mitochondrial bioenergetics 2015 ·Mitochondrion ·Angèle Nalbandian,Katrina J. Llewellyn,(unknown),(unknown),Hailing Su,(unknown),Marilyn Chwa,Jouni Vesa,M. Cristina Kenney,Virginia Kimonis	24
4	Global Gene Expression Profiling in R155H Knock-In Murine Model of VCP Disease 2014 ·Clinical and Translational Science ·Angèle Nalbandian,Svetlana Ghimbovschi,Zuyi Wang,Susan M. Knoblach,Katrina J. Llewellyn,Jouni Vesa,Eric P. Hoffman,Virginia Kimonis	3
5	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
6	A progressive translational mouse model of human valosin‐containing protein disease: The VCP^R155H/+ mouse 2012 ·Muscle & Nerve ·Angèle Nalbandian,Katrina J. Llewellyn,Mallikarjun Badadani,Hong Yin,Christopher Nguyen,(unknown),Giles Watts,Jogeshwar Mukherjee,Jouni Vesa,Vincent J. Caiozzo,Tahseen Mozaffar,John H. Weiss,Virginia Kimonis	51
7	The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget’s Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis 2011 ·Journal of Molecular Neuroscience ·Angèle Nalbandian,Sandra Donkervoort,Eric Dec,Mallikarjun Badadani,(unknown),(unknown),Christopher Nguyen,Jogeshwar Mukherjee,Vincent J. Caiozzo,Barbara J. Martin,Giles D. Watts,Jouni Vesa,Charles D. Smith,Virginia Kimonis	106
8	Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts 2009 ·Neuromuscular Disorders ·Jouni Vesa,Hailing Su,Giles D. Watts,Sabine Krause,Maggie C. Walter,Barbara J. Martin,Charles D. Smith,Douglas C. Wallace,Virginia Kimonis	54
9	VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: Review of a unique disorder 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Virginia Kimonis,Erin Fulchiero,Jouni Vesa,Giles Watts	169
10	Molecular and cellular characterization of the Down syndrome critical region protein 2 2005 ·Biochemical and Biophysical Research Communications ·Jouni Vesa,(unknown),(unknown),Julie R. Korenberg	9
11	A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging 2004 ·Human Molecular Genetics ·Outi Kopra,Jouni Vesa,Carina von Schantz,Tuula Manninen,(unknown),Anna‐Liisa Fabritius,Juhani Rapola,Otto P. van Diggelen,Janna Saarela,Anu Jalanko,Leena Peltonen	72
12	Mice with Ppt1Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons 2004 ·Neurobiology of Disease ·Anu Jalanko,Jouni Vesa,Tuula Manninen,Carina von Schantz,(unknown),Anna‐Liisa Fabritius,(unknown),Juhani Rapola,Massimiliano Gentile,Outi Kopra,Leena Peltonen	68
13	GRACILE Syndrome, a Lethal Metabolic Disorder with Iron Overload, Is Caused by a Point Mutation in BCS1L 2002 ·The American Journal of Human Genetics ·Ilona Visapää,Vineta Fellman,Jouni Vesa,Ayan Dasvarma,Jenna Hutton,Vijay Kumar,Gregory S. Payne,Marja Makarow,Rudy Van Coster,Robert W. Taylor,Douglass M. Turnbull,Anu Suomalainen,Leena Peltonen	199
14	Palmitoylation of the p75 neurotrophin receptor has no effect on its interaction with TrkA or on TrkA-mediated down-regulation of cell adhesion molecules 2000 ·Journal of Neuroscience Research ·Jouni Vesa,(unknown),José Miguel Cosgaya,Eric M. Shooter	7
15	p75 Reduces TrkB Tyrosine Autophosphorylation in Response to Brain-derived Neurotrophic Factor and Neurotrophin 4/5 2000 ·Journal of Biological Chemistry ·Jouni Vesa,Alex Krüttgen,Eric M. Shooter	44
16	From Locus to Cellular Disturbances: Positional Cloning of the Infantile Neuronal Ceroid Lipofuscinosis Gene 1997 ·Neuropediatrics ·Elina Hellsten,Jouni Vesa,Anu Jalanko,Leena Peltonen	7
17	Assignment of sterol carrier protein X/sterol carrier protein 2 to 1p32 and its exclusion as the causative gene for infantile neuronal ceroid lipofuscinosis 1994 ·Human Molecular Genetics ·Jouni Vesa,Elina Hellsten,(unknown),Beverly S. Emanuel,Jeffrey T. Billheimer,Scott Mead,John K. Cowell,Jerome F. Strauss,Leena Peltonen	10
18	Refined Assignment of the Infantile Neuronal Ceroid Lipofuscinosis (INCL, CLN1) Locus at 1p32: Incorporation of Linkage Disequilibrium in Multipoint Analysis 1993 ·Genomics ·Elina Hellsten,Jouni Vesa,Marcy C. Speer,Tomi P. Mäkelä,Irma Järvelä,Kari Alitalo,Jürg Ott,Leena Peltonen	58
19	Molecular Genetics of Neuronal Ceroid Lipofuscinoses 1992 ·Pediatric Research ·Irma Järvelä,Jouni Vesa,Pirkko Santavuori,Elina Hellsten,Leena Peltonen	18
20	DNA‐based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1) 1991 ·Prenatal Diagnosis ·Irma Järvelä,Juhani Rapola,Leena Peltonen,Lea Puhakka,Jouni Vesa,Pirkko Ämmälä,Riitta Salonen,Markku Ryynänen,P Haring,Aki Mustonen,Pirkko Santavuori	23

About Jouni Vesa

Jouni Vesa is a scholar working on Cell Biology, Physiology and Physiology, having authored 35 papers that have together received 2.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (16 papers), Cellular transport and secretion (9 papers) and Autophagy in Disease and Therapy (6 papers). The work is most often cited by research in Cell Biology (943 citations), Physiology (216 citations) and Physiology (1.0k citations). Jouni Vesa has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include Virginia Kimonis, Leena Peltonen, Elina Hellsten, Juhani Rapola, Pirkko Santavuori, Sandra L. Hofmann, Linda A. Verkruyse, Giles Watts, Emilie Tresse and Nico P. Dantuma. Their work appears in journals such as Nature, Journal of Biological Chemistry and PLoS ONE.

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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