Zamir Shorer

3.0k citations

67 papers · 2.1k indexed · h-index 25

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 5%
Psychiatry and Mental health top 5%
Neurology top 5%
Physiology top 10%

Co-authors: Ohad S. Birk Jacov Levy Hagit Flusser Rivka Ofir Ilan Shelef Bruria Ben‐Zeev Uri Kramer Eli Hershkovitz
Topics: Hereditary Neurological Disorders (13 papers)Epilepsy research and treatment (13 papers)Pharmacological Effects and Toxicity Studies (7 papers)
Cited by: Cellular and Molecular Neuroscience Neurology Psychiatry and Mental health
Journals: Proceedings of the National Academy of Sciences Blood Brain
Partner nations: Israel United States Canada

In The Last Decade

Zamir Shorer

67 papers receiving 2.0k citations

Peers

Countries citing papers authored by Zamir Shorer

Since Specialization

Citations

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

Fields of papers citing papers by Zamir Shorer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zamir Shorer

This figure shows the co-authorship network connecting the top 25 collaborators of Zamir Shorer. A scholar is included among the top collaborators of Zamir Shorer 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 Zamir Shorer. Zamir Shorer 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	Correlates of Caregiving Burden among Bedouin-Muslim Mothers of Children Diagnosed with Epilepsy 2022 ·International Journal of Environmental Research and Public Health ·(unknown),(unknown),Zamir Shorer,Yaacov G. Bachner	3
2	Phenotypic variability and mutation hotspot in COX15‐related Leigh syndrome 2020 ·American Journal of Medical Genetics Part A ·Daniel Halpérin,(unknown),Ohad Wormser,Yuval Yogev,(unknown),Zamir Shorer,Libe Gradstein,Ilan Shelef,Hagit Flusser,Ohad S. Birk	9
3	SEC31A mutation affects ER homeostasis, causing a neurological syndrome 2018 ·Journal of Medical Genetics ·Daniel Halpérin,Rotem Kadir,Yonatan Perez,(unknown),Yuval Yogev,Ohad Wormser,(unknown),Ekaterina Eremenko,Barak Rotblat,Zamir Shorer,Libe Gradstein,Ilan Shelef,Ruth Birk,Uri Abdu,Hagit Flusser,Ohad S. Birk	27
4	Novel SBF1 splice‐site null mutation broadens the clinical spectrum of Charcot‐Marie‐Tooth type 4B3 disease 2018 ·Clinical Genetics ·Hagit Flusser,Daniel Halpérin,Rotem Kadir,Zamir Shorer,Ilan Shelef,Ohad S. Birk	11
5	Temporal lobe surgery for intractable epilepsy in children: What to do with the hippocampus? 2017 ·Seizure ·Mony Benifla,(unknown),Zamir Shorer,Iris Noyman,(unknown),Dana Ekstein	7
6	New DSM-5 criteria for ADHD — Does it matter? 2016 ·Comprehensive Psychiatry ·(unknown),Iris Manor,(unknown),Zamir Shorer,Iris Noyman,Yair Sadaka	21
7	CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay 2015 ·Human Molecular Genetics ·Michael Volodarsky,Hava Lichtig,Tom Leibson,Yair Sadaka,Rotem Kadir,Yonatan Perez,(unknown),Libe Gradstein,Ruthy Shaco‐Levy,Zamir Shorer,Dale Frank,Ohad S. Birk	12
8	A Novel Mutation in SCN9A in a Child With Congenital Insensitivity to Pain 2013 ·Pediatric Neurology ·Zamir Shorer,(unknown),(unknown),Jacov Levy,Ruti Parvari	17
9	CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy 2012 ·Blood ·Yoram Nevo,Bruria Ben‐Zeev,Adi Tabib,Rachel Straussberg,Yair Anikster,Zamir Shorer,Aviva Fattal‐Valevski,Asaf Ta‐Shma,Sharon Aharoni,Malcolm Rabie,Shamir Zenvirt,Hanoch Goldshmidt,Yakov Fellig,Avraham Shaag,Dror Mevorach,Orly Elpeleg	111
10	Immunoglobulin Treatment for Severe Childhood Epilepsy 2012 ·Pediatric Neurology ·(unknown),Zamir Shorer,Shay Menascu,Ilan Linder,Hadassah Goldberg‐Stern,Eli Heyman,T. Lerman‐Sagie,Bruria Ben Zeev,Uri Kramer	20
11	Changes in Cerebral Venous Sinuses Diameter After Lumbar Puncture in Idiopathic Intracranial Hypertension: A Prospective MRI Study 2012 ·Journal of Neuroimaging ·Anat Horev,(unknown),Ygal Plakht,Zamir Shorer,Itzhak Wirguin,Ilan Shelef	52
12	Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation 2010 ·The American Journal of Human Genetics ·(unknown),Barak Markus,Iris Noyman,(unknown),Hagit Flusser,Ilan Shelef,(unknown),Zamir Shorer,Idan Cohen,(unknown),Sara Sivan,Ohad S. Birk	62
13	Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 2008 ·The American Journal of Human Genetics ·Ortal Barel,Stavit A. Shalev,Rivka Ofir,Asi Cohen,Joël Zlotogora,Zamir Shorer,(unknown),Gal Finer,(unknown),Noam Zilberberg,Ohad S. Birk	137
14	Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ 2008 ·The American Journal of Human Genetics ·Ortal Barel,Zamir Shorer,Hagit Flusser,Rivka Ofir,Ginat Narkis,Gal Finer,(unknown),(unknown),Ann Saada,Ohad S. Birk	92
15	PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy 2006 ·The American Journal of Human Genetics ·(unknown),Hagit Flusser,Rivka Ofir,Ilan Shelef,Ginat Narkis,Gideon Vardi,Zamir Shorer,Rachel Lévy,Aharon Galil,Khalil Elbedour,Ohad S. Birk	145
16	Nerve Growth Factor-Tyrosine Kinase A Pathway Is Involved in Thermoregulation and Adaptation to Stress: Studies on Patients with Hereditary Sensory and Autonomic Neuropathy Type IV 2005 ·Pediatric Research ·Neta Loewenthal,Jacov Levy,Ruth Schreiber,Vered Pinsk,Zvi Perry,Zamir Shorer,Eli Hershkovitz	15
17	Adverse reactions of Topiramate and Lamotrigine in children 2004 ·Pharmacoepidemiology and Drug Safety ·(unknown),Zamir Shorer,Uri Kramer,Tally Lerman‐Sagie,(unknown),(unknown),Rafael Gorodischer	11
18	Neurophysiologic studies in congenital insensitivity to pain with anhidrosis 2001 ·Pediatric Neurology ·Zamir Shorer,Shimon Moses,Eli Hershkovitz,Vered Pinsk,Jacov Levy	31
19	Outcome of infants with unilateral Sturge-Weber syndrome and early onset seizures 2000 ·Developmental Medicine & Child Neurology ·Uri Kramer,Esther Kahana,Zamir Shorer,Bruria Ben‐Zeev	56
20	Multiplede novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas case 1997 ·Human Mutation ·Laura E. Warner,Mordechai Shohat,Zamir Shorer,James R. Lupski	21

About Zamir Shorer

Zamir Shorer is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Neurology, having authored 67 papers that have together received 2.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (13 papers), Epilepsy research and treatment (13 papers) and Pharmacological Effects and Toxicity Studies (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (534 citations), Neurology (203 citations) and Psychiatry and Mental health (348 citations). Zamir Shorer has collaborated with scholars based in Israel, United States and Canada. Frequent co-authors include Ohad S. Birk, Jacov Levy, Hagit Flusser, Rivka Ofir, Ilan Shelef, Bruria Ben‐Zeev, Uri Kramer, Eli Hershkovitz, Giora Pillar and Eli Peled. Their work appears in journals such as Proceedings of the National Academy of Sciences, Blood and Brain.

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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