Yonatan Perez

2.4k citations

27 papers · 1.1k indexed · 1 hit paper · h-index 14

Impact in

Neurology top 5%
- Neuroinflammation and Neurodegeneration Mechanisms
Developmental Neuroscience top 10%

Papers in

Molecular Biology 24
- Ion channel regulation and function 4
- Single-cell and spatial transcriptomics 3
- CRISPR and Genetic Engineering 3
- RNA regulation and disease 3
- RNA modifications and cancer 3
- RNA Research and Splicing 3
- Mitochondrial Function and Pathology 2
- Biochemical and Molecular Research 2
Cell Biology 4

Co-authors: Arnold R. Kriegstein Lucas Schirmer Simone Mayer Dmitry Velmeshev Aparna Bhaduri Maximilian Haeussler David H. Rowitch Ohad S. Birk
Journals: European Journal of Human Genetics (3 papers)Brain (3 papers)Journal of Medical Genetics (3 papers)Nature Communications (2 papers)Science (2 papers)
Partner nations: Israel United States United Kingdom

In The Last Decade

Yonatan Perez

26 papers receiving 1.1k citations

Hit Papers

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Single-cell genomics identifies cell type–specific molecular changes in autism 2019 · 506 citations

Peers

Countries citing papers authored by Yonatan Perez

Since Specialization

Citations

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

Fields of papers citing papers by Yonatan Perez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Yonatan Perez, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yonatan Perez Line = papers co-authored together Yonatan Perez links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Single-cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism Nature Communications ·Yonatan Perez, Dmitry Velmeshev, Li Wang, Thomas L. Reichmann, Roger Chavez, Michael Bryan, 程波林, Joyce Lara de Lima Mendes, Songcang Chen, Soukaina DARAMI, Wallace T. Burnett, Shaohui Wang, Brittney Wick, Maximilian Haeussler, Stormy J. Chamberlain, Arturo Álvarez-Buylla, Arnold R. Kriegstein	2025	0
2	G-protein-coupled receptor ADGRG1 drives a protective microglial state in Alzheimer's disease through MYC activation Neuron ·P. V. Malvin, Andi Wangzhou, Diankun Yu, Tao Li, Adrián Delgado, Jeffrey Thomas Hewlett, Shengru Zhou, Helena Bistrović, J. Wang, Beastall Gh, Yonatan Perez, Lea T. Grinberg, Salvatore Spina, Richard M. Ransohoff, Arnold R. Kriegstein, William W. Seeley, Tomasz J. Nowakowski, A. Zapletálek	2025	2
3	ZNF142 mutation causes sex-dependent neurologic disorder Journal of Medical Genetics ·Sabrina Lehrer, Marina Eskin‐Schwartz, Zamir Shorer, Rotem Kadir, Daniel Halpérin, E. Egorchenkova, Yuval Yogev, Sinara Mônica de Oliveira Leite, Niki Jeannin, Hagit Cohen, Ekaterina Eremenko, Yonatan Perez, Ohad S. Birk	2024	2
4	IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma npj Genomic Medicine ·Ohad Wormser, Yonatan Perez, Simone Cohen-LÃ©on, Kati Mönkkönen, Nigussie Tadesse, Libe Gradstein, Yuval Yogev, Niki Jeannin, A. Abou-Zeid, E. Egorchenkova, Daniel Halpérin, 正登中山, Julia Lais Da Silva Machado, Katia Del Rio‐Tsonis, Ramon Y. Birnbaum, Lakshma Reddy Vuyyuru, Ohad S. Birk	2023	1
5	Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone Proceedings of the National Academy of Sciences ·Yuval Yogev, Zamir Shorer, Arie Koifman, Ohad Wormser, E. Egorchenkova, Daniel Halpérin, Simone Cohen-LÃ©on, Sabrina Lehrer, Niki Jeannin, Geula Davidov, Г. И. Шарафиева, Raz Zarivach, Ilan Shelef, Yonatan Perez, Ohad S. Birk	2023	21
6	The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences Investigative Ophthalmology & Visual Science ·Bestaeva N.V. Bestaeva, Libe Gradstein, Arthur A. Bergen, Ralph J. Florijn, Benoı̂t Arveiler, Eulalie Lasseaux, Xavier Zanlonghi, Pep Aguiló Fuster, Anne B. Fulton, Claudia Yahalom, Anat Blumenfeld, Yonatan Perez, Ohad S. Birk, Gerard C. de Wit, Nicoline E. Schalij‐Delfos, Maria M. van Genderen	2022	10
7	CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice Nature Communications ·Daniel Halpérin, Hamza Wazir Khan, Rotem Kadir, E. Egorchenkova, Ohad Wormser, Yuval Yogev, Simone Cohen-LÃ©on, Sabrina Lehrer, Yonatan Perez, Г. И. Шарафиева, Aisa Nikmah Rahmatih, Barak Rotblat, Tzuri Lifschytz, Amit Lotan, Gal Meiri, Daniel Gitler, Ohad S. Birk	2021	23
8	Single-cell genomics identifies cell type–specific molecular changes in autism Science ·Dmitry Velmeshev, Lucas Schirmer, P. Malliga, Maximilian Haeussler, Yonatan Perez, Simone Mayer, Aparna Bhaduri, W. J. Birch, David H. Rowitch, Arnold R. Kriegstein Hit paper breakdown →	2019	506
9	Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenase Journal of Clinical Investigation ·E. Egorchenkova, Yuval Yogev, Lior Zeller, Raz Zarivach, Ran Zalk, Daniel Halpérin, Ohad Wormser, Rosemary Kayanda, Daniel Landau, Rotem Kadir, Yonatan Perez, Ohad S. Birk	2019	29
10	SEC31A mutation affects ER homeostasis, causing a neurological syndrome Journal of Medical Genetics ·Daniel Halpérin, Rotem Kadir, Yonatan Perez, E. Egorchenkova, Yuval Yogev, Ohad Wormser, J.P Silva, Ekaterina Eremenko, Barak Rotblat, Zamir Shorer, Libe Gradstein, Ilan Shelef, Ruth Birk, Uri Abdu, Hagit Flusser, Ohad S. Birk	2018	27
11	RSRC1 mutation affects intellect and behaviour through aberrant splicing and transcription, downregulating IGFBP3 Brain ·Yonatan Perez, Shay Menascu, Idan Cohen, Rotem Kadir, Omer Basha, Zamir Shorer, Хмарик Александр Геннадьевич, Gal Meiri, Veronika Selzam, Rivka Ofir, Esti Yeger‐Lotem, Ohad S. Birk	2018	16
12	Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe American Journal of Medical Genetics Part A ·Ohad Wormser, Libe Gradstein, K. Deutschmann, Yuval Yogev, Yonatan Perez, J. Marberg, Khalil Elbedour, E. Egorchenkova, Barak Markus, Rotem Kadir, Daniel Halpérin, SEVDA HOCAOĞLU, Jaime Levy, Tova Lifshitz, Esther Manor, Ohad S. Birk	2018	2
13	Progressive hereditary spastic paraplegia caused by a homozygous KY mutation European Journal of Human Genetics ·Yuval Yogev, Yonatan Perez, Iris Noyman, Brisa Pozzi de [UNESP] Sousa, Hagit Flusser, Zamir Shorer, A. J. Spence, Leonid Kachko, Chughtai Imran Rafiq, Ruth Birk, Arie Koifman, E. Egorchenkova, Ohad Wormser, Daniel Halpérin, Rotem Kadir, Ohad S. Birk	2017	13
14	A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion American Journal of Medical Genetics Part A ·Idan Cohen, Orna Staretz‐Chacham, Ohad Wormser, Yonatan Perez, Ann Saada, Rotem Kadir, Ohad S. Birk	2017	13
15	SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome Brain ·Yonatan Perez, Zamir Shorer, Gryssel Rodríguez, Pauline Chabosseau, Rotem Kadir, Michael Volodarsky, Daniel Halpérin, S. Barber-Zucker, Hanna Shalev, Ruth Schreiber, Libe Gradstein, Rosemary Kayanda, Raz Zarivach, Guy A. Rutter, Daniel Landau, Ohad S. Birk	2017	71
16	Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred BMC Medical Genetics ·Libe Gradstein, H Gougerot, Yuri V. Sergeev, Itay Lavy, Ginat Narkis, Yonatan Perez, Antoine. Auteur du texte Duplan, Dror Sharon, Eyal Banin, 豊湯田, Tova Lifshitz, Ohad S. Birk	2016	13
17	ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size PLoS Genetics ·Rotem Kadir, Tamar Harel, Barak Markus, Yonatan Perez, Anna Bakhrat, Idan Cohen, Michael Volodarsky, Paran Kiritharamohan, Morgan K. Eichorst, Joël Zlotogora, Sara Sivan, Ramon Y. Birnbaum, Uri Abdu, Stavit A. Shalev, Ohad S. Birk	2016	62
18	CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay Human Molecular Genetics ·Michael Volodarsky, Hava Lichtig, Tom Leibson, Yair Sadaka, Rotem Kadir, Yonatan Perez, Gryssel Rodríguez, Libe Gradstein, Ruthy Shaco‐Levy, Zamir Shorer, Dale Frank, Ohad S. Birk	2015	12
19	Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation European Journal of Human Genetics ·Yonatan Perez, Libe Gradstein, Hagit Flusser, Barak Markus, Idan Cohen, Vivica Messner, Dongyong Yao, Tova Lifshitz, Rotem Kadir, Ohad S. Birk	2013	38
20	Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase European Journal of Human Genetics ·Idan Cohen, Eldad Silberstein, Yonatan Perez, Daniella Landau, Khalil Elbedour, Vivica Messner, Rotem Kadir, Michael Volodarsky, Sara Sivan, Ginat Narkis, Ohad S. Birk	2013	45

About Yonatan Perez

Yonatan Perez is a scholar working on Molecular Biology, Cell Biology, Developmental Neuroscience, Nutrition and Dietetics and Genetics, having authored 27 papers that have together received 1.1k indexed citations. Recurring topics across this work include Ion channel regulation and function (4 papers), Single-cell and spatial transcriptomics (3 papers), CRISPR and Genetic Engineering (3 papers), RNA regulation and disease (3 papers), RNA modifications and cancer (3 papers), RNA Research and Splicing (3 papers), Mitochondrial Function and Pathology (2 papers) and Biochemical and Molecular Research (2 papers). The work is most often cited by research in Neurology (146 citations), Developmental Neuroscience (60 citations), Molecular Biology (728 citations), Biological Psychiatry (26 citations) and Genetics (248 citations). Yonatan Perez has collaborated with scholars based in Israel, United States and United Kingdom. Frequent co-authors include Arnold R. Kriegstein, Lucas Schirmer, Simone Mayer, Dmitry Velmeshev, Aparna Bhaduri, Maximilian Haeussler, David H. Rowitch, Ohad S. Birk, Rotem Kadir and Michael Volodarsky. Their work appears in journals such as European Journal of Human Genetics, Brain, Journal of Medical Genetics, Nature Communications and Science.

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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