Moien Kanaan

4.7k total citations
58 papers, 2.2k citations indexed

About

Moien Kanaan is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Moien Kanaan has authored 58 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 18 papers in Sensory Systems and 17 papers in Genetics. Recurrent topics in Moien Kanaan's work include Hearing, Cochlea, Tinnitus, Genetics (18 papers), Connexins and lens biology (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Moien Kanaan is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (18 papers), Connexins and lens biology (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Moien Kanaan collaborates with scholars based in Israel, Palestinian Territory and United States. Moien Kanaan's co-authors include Karen B. Avraham, Hashem Shahin, Mary‐Claire King, Tom Walsh, Ming K. Lee, Amal Abu Rayyan, Tama Sobe, George A. Marzluf, Sarah Vreugde and Ephrat Levy‐Lahad and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Investigation.

In The Last Decade

Moien Kanaan

56 papers receiving 2.2k citations

Peers

Countries citing papers authored by Moien Kanaan

Since Specialization

Citations

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

Fields of papers citing papers by Moien Kanaan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moien Kanaan

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancers 2024 ·JNCI Journal of the National Cancer Institute ·(unknown), Sari Lieberman, (unknown), (unknown), Ming K. Lee, Süleyman Gülsüner, (unknown), Rachel Beeri, Amal Abu Rayyan, Jessica B. Mandell, Hila Fridman, (unknown), (unknown), (unknown), Amnon Lahad, Mary‐Claire King, Ephrat Levy‐Lahad, Moien Kanaan	0
2	A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss 2023 ·Human Molecular Genetics ·Amal Abu Rayyan, Ryan J. Carlson, (unknown), Ming K. Lee, Süleyman Gülsüner, Tom Walsh, Karen B. Avraham, Moien Kanaan, Mary‐Claire King	0
3	An SNX10-dependent mechanism downregulates fusion between mature osteoclasts 2021 ·Journal of Cell Science ·Maayan Barnea, Sabina Winograd‐Katz, Moran Shalev, Esther Arman, Nina Reuven, L. E. Roth, Ofra Golani, Merle Stein, (unknown), Moien Kanaan, Jan Tuckermann, Benjamin Geiger, Ari Elson	12
4	A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay 2021 ·Neurobiology of Aging ·Marc Gotkine, Martina de Majo, Chun Hao Wong, Simon Topp, Rachel Michaelson‐Cohen, Silvina Epsztejn‐Litman, Rachel Eiges, (unknown), Moien Kanaan, (unknown), (unknown), Caroline Vance, Stephen Newhouse, Gerome Breen, Agnes L. Nishimura, Christopher E. Shaw, Bradley Smith	5
5	Genomic analysis of inherited hearing loss in the Palestinian population 2020 ·Proceedings of the National Academy of Sciences ·Amal Abu Rayyan, (unknown), Silvia Casadei, Zippora Brownstein, (unknown), Hashem Shahin, Christina Canavati, (unknown), (unknown), (unknown), Ryan J. Carlson, Süleyman Gülsüner, Ming K. Lee, Karen B. Avraham, Tom Walsh, Mary‐Claire King, Moien Kanaan	38
6	Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities 2020 ·Molecular Case Studies ·(unknown), Sarah B. Pierce, Christina Canavati, Amal Abu Rayyan, (unknown), (unknown), (unknown), Barbara M. Norquist, (unknown), (unknown), Ephrat Levy‐Lahad, Mary‐Claire King, Moien Kanaan	5
7	Massive osteopetrosis caused by non-functional osteoclasts in R51Q SNX10 mutant mice 2020 ·Bone ·Merle Stein, Maayan Barnea, Moran Shalev, Esther Arman, Ori Brenner, Sabina Winograd‐Katz, (unknown), (unknown), Moien Kanaan, Hila Elinav, Polina Stepensky, Benjamin Geiger, Jan Tuckermann, Ari Elson	9
8	The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizures 2017 ·Journal of Neurology ·Karl Martin Klein, Manuela Pendziwiat, Anda Eilam, Ronit Gilad, Ilan Blatt, Felix Rosenow, Moien Kanaan, Ingo Helbig, Zaid Afawi	19
9	Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress 2015 ·Journal of Medical Genetics ·Ariella Weinberg‐Shukron, Abdulsalam Abu‐Libdeh, (unknown), Liran Carmel, Aviram Kogot‐Levin, (unknown), Moien Kanaan, Sharon Zeligson, Paul Renbaum, Ephrat Levy‐Lahad, David Zangen	28
10	Genomic advances for gene discovery in hereditary hearing loss 2012 ·Journal of Basic and Clinical Physiology and Pharmacology ·Karen B. Avraham, Moien Kanaan	11
11	GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome 2012 ·The American Journal of Human Genetics ·Dan Doherty, Albert E. Chudley, Gail Coghlan, Gisele E. Ishak, A. Micheil Innes, Edmond G. Lemire, R. Curtis Rogers, Aizeddin A. Mhanni, Ian G. Phelps, Steven J.M. Jones, Shing H. Zhan, Anthony P. Fejes, Hashem Shahin, Moien Kanaan, Hatice Akay, Mustafa Tekin, Barbara L. Triggs‐Raine, Teresa Zelinski	2
12	XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription 2011 ·The American Journal of Human Genetics ·David Zangen, Yotam Kaufman, Sharon Zeligson, (unknown), Hila Fridman, Moien Kanaan, (unknown), Abdulsalam Abu‐Libdeh, Ayal B. Gussow, (unknown), Liran Carmel, Paul Renbaum, Ephrat Levy‐Lahad	78
13	Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84 2010 ·Journal of Medical Genetics ·Hashem Shahin, (unknown), Amal Rayan, Karen B. Avraham, Mary‐Claire King, Moien Kanaan, Tom Walsh	34
14	Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82 2010 ·The American Journal of Human Genetics ·Tom Walsh, Hashem Shahin, T. Elkan Miller, Ming K. Lee, Anne Thornton, Wendy Roeb, Amal Abu Rayyan, (unknown), Karen B. Avraham, Mary‐Claire King, Moien Kanaan	198
15	Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51 2010 ·The American Journal of Human Genetics ·Tom Walsh, Sarah B. Pierce, Danielle R. Lenz, Zippora Brownstein, Orit Dagan‐Rosenfeld, Hashem Shahin, Wendy Roeb, Shane McCarthy, Alex S. Nord, Carlos R. Gordon, Ziva Ben‐Neriah, Jonathan Sebat, Moien Kanaan, Ming K. Lee, Moshe Frydman, Mary‐Claire King, Karen B. Avraham	74
16	Molecular Epidemiology of Hereditary Epidermolysis Bullosa in a Middle Eastern Population 2006 ·Journal of Investigative Dermatology ·(unknown), Margarita Indelman, Ellen G Pfendner, Tzipora C. Falik‐Zaccai, (unknown), Stavit A. Shalev, (unknown), (unknown), (unknown), (unknown), Ruth Gershoni‐Baruch, Morad Khayat, (unknown), Gabriele Richard, Richard N. Bergman, Jouni Uitto, Moien Kanaan, Eli Sprecher	42
17	Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss 2005 ·The American Journal of Human Genetics ·Hashem Shahin, Tom Walsh, Tama Sobe, (unknown), Amal Rayan, Eric D. Lynch, Ming K. Lee, Karen B. Avraham, Mary‐Claire King, Moien Kanaan	85
18	Promoting Arab and Israeli cooperation: peacebuilding through health initiatives 2005 ·The Lancet ·Harvey A. Skinner, Ziad Abdeen, (unknown), (unknown), M. S. Al-Masri, Joseph Attias, Karen B. Avraham, Rivka Carmi, (unknown), (unknown), (unknown), (unknown), Moien Kanaan, Hillel Pratt, (unknown), Yehudah Roth, A. Paul Williams, Arnold M. Noyek	25
19	From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 2002 ·Proceedings of the National Academy of Sciences ·Tom Walsh, (unknown), Sarah Vreugde, Ronna Hertzano, Hashem Shahin, (unknown), Ming K. Lee, Moien Kanaan, Mary‐Claire King, Karen B. Avraham	170
20	Junctional epidermolysis bullosa in the Middle East: Clinical and genetic studies in a series of consanguineous families 2002 ·Journal of the American Academy of Dermatology ·Aoi Nakano, Gilles G. Lestringant, Tamar Paperna, Richard N. Bergman, Ruth Gershoni, Philippe Frossard, Moien Kanaan, Guerrino Meneguzzi, Gabriele Richard, Ellen G Pfendner, Jouni Uitto, Leena Pulkkinen, Eli Sprecher	37

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.

Explore authors with similar magnitude of impact