Maria Kousi

3.4k total citations · 1 hit paper
15 papers, 1.2k citations indexed

About

Maria Kousi is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Maria Kousi has authored 15 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Physiology. Recurrent topics in Maria Kousi's work include Cellular transport and secretion (3 papers), Lysosomal Storage Disorders Research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Maria Kousi is often cited by papers focused on Cellular transport and secretion (3 papers), Lysosomal Storage Disorders Research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Maria Kousi collaborates with scholars based in United States, Finland and United Kingdom. Maria Kousi's co-authors include Nicholas Katsanis, Anna‐Elina Lehesjoki, Sara Mole, Benjamin M. Neale, Patrick F. Sullivan, Steven A. McCarroll, Hyejung Won, Michael O’Donovan, Alkes L. Price and Nicholas Mancuso and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Maria Kousi

15 papers receiving 1.2k 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.

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

2018 293 citations Alexander Gusev, Nicholas Mancuso et al. Nature Genetics profile →

Peers

Maria Kousi

MB

PHYSI

GENET

CB

CMN

Coro Paisán‐Ruiz United States

Klaus Rüether Germany

Elena Ambrosini Italy

Mark J. Zylka United States

Martine Jodar France

C. Henrique Alves Netherlands

Amy Strickland United States

Una‐Marie Sheerin United Kingdom

Kim M. Hemsley Australia

Elías Utreras Chile

Coro Paisán‐Ruiz United States

Maria Kousi

479 ×0.8

MB

166 ×0.4

PHYSI

237 ×0.7

GENET

223 ×0.9

CB

322 ×1.9

CMN

Citations per year, relative to Maria Kousi Maria Kousi (= 1×) peers Coro Paisán‐Ruiz

Countries citing papers authored by Maria Kousi

Since Specialization

Citations

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

Fields of papers citing papers by Maria Kousi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Kousi

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Kousi. A scholar is included among the top collaborators of Maria Kousi 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 Maria Kousi. Maria Kousi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

1.

Kousi, Maria, Onuralp Söylemez, Niki Mourtzi, et al.. (2020). Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy. Nature Genetics. 52(11). 1145–1150. 21 indexed citations

2.

Monroe, Tanner O., Melanie E. Garrett, Maria Kousi, et al.. (2020). PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia. Nature Communications. 11(1). 5903–5903. 19 indexed citations

3.

Spataro, Rossella, Maria Kousi, Sali M.K. Farhan, et al.. (2019). Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion. Human Genomics. 13(1). 19–19. 34 indexed citations

4.

Gusev, Alexander, Nicholas Mancuso, Hyejung Won, et al.. (2018). Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights. Nature Genetics. 50(4). 538–548. 293 indexed citations breakdown →

5.

Kousi, Maria, Maria Suo‐Palosaari, Jukka S. Moilanen, et al.. (2018). Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases. Neuropediatrics. 49(4). 256–261. 7 indexed citations

6.

Ylikallio, Emil, Mari Auranen, I. Mahjneh, et al.. (2016). Decreased Aerobic Capacity in ANO5-Muscular Dystrophy. Journal of Neuromuscular Diseases. 3(4). 475–485. 6 indexed citations

7.

Kousi, Maria & Nicholas Katsanis. (2016). The Genetic Basis of Hydrocephalus. Annual Review of Neuroscience. 39(1). 409–435. 72 indexed citations

8.

Kousi, Maria & Nicholas Katsanis. (2015). Genetic Modifiers and Oligogenic Inheritance. Cold Spring Harbor Perspectives in Medicine. 5(6). a017145–a017145. 77 indexed citations

9.

Nesin, Vasyl, Graham B. Wiley, Maria Kousi, et al.. (2014). Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis. Proceedings of the National Academy of Sciences. 111(11). 4197–4202. 180 indexed citations

10.

Kousi, Maria, Verneri Anttila, Angela Schulz, et al.. (2012). Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene. Journal of Medical Genetics. 49(6). 391–399. 55 indexed citations

11.

Kousi, Maria. (2012). DISSECTION OF THE GENETIC BACKGROUND OF CHILDHOOD ONSET PROGRESSIVE MYOCLONIC EPILEPSIES. Työväentutkimus Vuosikirja. 1 indexed citations

12.

Kousi, Maria, Anna‐Elina Lehesjoki, & Sara Mole. (2011). Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses. Human Mutation. 33(1). 42–63. 257 indexed citations

13.

Kousi, Maria, Corinne Sagné, Gian Carlo Bellenchi, et al.. (2010). Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis. Human Molecular Genetics. 19(22). 4497–4514. 44 indexed citations

14.

Sirén, Auli, Anne Polvi, Malgorzata Labuda, et al.. (2009). Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q. Epilepsy Research. 88(1). 65–75. 14 indexed citations

15.

Kousi, Maria, Eija Siintola, Lenka Dvořáková, et al.. (2009). Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis. Brain. 132(3). 810–819. 94 indexed citations

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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