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Moien Kanaan

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Kemal O Yariz; Juan I. Young; Suna Tokgoz-Yilmaz; Semra Atalay; S Blanton; Zheng-Yi Chen; Julia Dallman; Alexandra A Desmidt; Oscar Diaz-Horta; Duygu Duman; Yvonne Jemimah Edwards; Lisette Hetterschijt; Mingqian Huang; Moien Kanaan; Ozlem Konukseven; Hannie Kremer; Huawei Li; Xue-Zhong Liu; Na Lu; Zhongmin Lu; Anne M M Oonk; Jaap Oostrik; Ronald J E Pennings; Theo A Peters; Margit Schraders; Celia Zazo Seco; Hashem Shahin; Asli Sirmaci; Isaac Skromne; Mustafa Tekin
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.
Dan Doherty; Anthony P Fejes; A Micheil Innes; Gisele E Ishak; Steven J M Jones; Moien Kanaan; Edmond G Lemire; Aizeddin A Mhanni; Ian G Phelps; R Curtis Rogers; Hashem Shahin; Mustafa Tekin; Barbara L Triggs-Raine; Hatice Akay; Albert E Chudley; Gail Coghlan; Shing H Zhan; Teresa Zelinski
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome.
Karen B Avraham; Moien Kanaan
Genomic advances for gene discovery in hereditary hearing loss.

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All Publications

2012: Kemal O Yariz; Juan I. Young; Suna Tokgoz-Yilmaz; Semra Atalay; S Blanton; Zheng-Yi Chen; Julia Dallman; Alexandra A Desmidt; Oscar Diaz-Horta; Duygu Duman; Yvonne Jemimah Edwards; Lisette Hetterschijt; Mingqian Huang; Moien Kanaan; Ozlem Konukseven; Hannie Kremer; Huawei Li; Xue-Zhong Liu; Na Lu; Zhongmin Lu; Anne M M Oonk; Jaap Oostrik; Ronald J E Pennings; Theo A Peters; Margit Schraders; Celia Zazo Seco; Hashem Shahin; Asli Sirmaci; Isaac Skromne; Mustafa Tekin
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.
American journal of human genetics 2012;91(5):872-82.
2012: Dan Doherty; Anthony P Fejes; A Micheil Innes; Gisele E Ishak; Steven J M Jones; Moien Kanaan; Edmond G Lemire; Aizeddin A Mhanni; Ian G Phelps; R Curtis Rogers; Hashem Shahin; Mustafa Tekin; Barbara L Triggs-Raine; Hatice Akay; Albert E Chudley; Gail Coghlan; Shing H Zhan; Teresa Zelinski
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome.
American journal of human genetics 2012;90(6):1088-93.
2012: Karen B Avraham; Moien Kanaan
Genomic advances for gene discovery in hereditary hearing loss.
Journal of basic and clinical physiology and pharmacology 2012;23(3):93-7.
2011: Silvia Dossena; Moien Kanaan; Charity Nofziger; Karen B Avraham; Zippora Brownstein; Markus Paulmichl
Functional characterization of pendrin mutations found in the Israeli and Palestinian populations.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2011;28(3):477-84.
2011: Zippora Brownstein; Bella Davidov; Lilach Friedman; Moshe Frydman; Moien Kanaan; Mary-Claire King; Nitzan Kol; Ming K Lee; Dorit Lev; Ephrat Levy-Lahad; Sari Lieberman; Varda Oron-Karni; Thomas Parzefall; Michele Rahile; Hashem Shahin; Stavit Shalev; Mordechai Shohat; Noam Shomron; Tom Walsh; Amal Abu Rayyan; Karen B Avraham
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families.
Genome biology 2011;12(9):R89.
2011: Randa Kattan; Amal Abu Rayyan; Inas Zheiman; Suzan Idkeidek; Sabri Baraghithi; Nabeel Rishmawi; Sultan Turkuman; Afaf Abu-Diab; Riyad Ghneim; Madeleine Zoughbi; Rula Dauodi; Raed Ghneim; Abed-El-Razeq Issa; Issa Siryani; Randa Al Qas; Rawan Liddawi; Hatem Khamash; Moien Kanaan; Hiyam Marzouqa; Musa Y Hindiyeh
Serotype distribution and drug resistance in Streptococcus pneumoniae, Palestinian Territories.
Emerging infectious diseases 2011;17(1):94-6.
2010: Hashem Shahin; Michael Rahil; Amal Abu Rayan; Karen B Avraham; Mary-Claire King; Moien Kanaan; Tom Walsh
Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84.
Journal of medical genetics 2010;47(9):643-5.
2010: Tayfun Ozçelik; Moien Kanaan; Karen B Avraham; Drakoulis Yannoukakos; André Mégarbané; Ghazi O Tadmouri; Lefkos Middleton; Giovanni Romeo; Mary-Claire King; Ephrat Levy-Lahad
Collaborative genomics for human health and cooperation in the Mediterranean region.
Nature genetics 2010;42(8):641-5.
2010: 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
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.
American journal of human genetics 2010;87(1):101-9.
2010: Tom Walsh; Hashem Shahin; Tal Elkan-Miller; Ming K Lee; Anne M Thornton; Wendy Roeb; Amal Abu Rayyan; Suheir Loulus; Karen B Avraham; Mary-Claire King; Moien Kanaan
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.
American journal of human genetics 2010;87(1):90-4.
2010: Asli Sirmaci; Seyra Erbek; Justin Price; Mingqian Huang; Duygu Duman; Filiz Basak Cengiz; Güney Bademci; Suna Tokgöz-Yilmaz; Burcu Hişmi; Hilal Ozdağ; Banu Oztürk; Sevsen Kulaksizoğlu; Erkan Yildirim; Haris Kokotas; Maria Grigoriadou; Michael B Petersen; Hashem Shahin; Moien Kanaan; Mary-Claire King; Zheng-Yi Chen; S Blanton; Xue Zhong Liu; Stephan Zuchner; Nejat Akar; Mustafa Tekin
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.
American journal of human genetics 2010;86(5):797-804.
2010: Hashem Shahin; Tom Walsh; Amal Abu Rayyan; Ming K Lee; Jake Higgins; Diane Dickel; Kristen Lewis; James Thompson; Carl Baker; Alex S Nord; Sunday Stray; David Gurwitz; Karen B Avraham; Mary-Claire King; Moien Kanaan
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
European journal of human genetics : EJHG 2010;18(4):407-13.
1995: F Müller; D Krüger; Evelyn Sattlegger; B Hoffmann; P Ballario; Moien Kanaan; I B Barthelmess
The cpc-2 gene of Neurospora crassa encodes a protein entirely composed of WD-repeat segments that is involved in general amino acid control and female fertility.
Molecular & general genetics : MGG 1995;248(2):162-73.
1993: Moien Kanaan; George A Marzluf
The positive-acting sulfur regulatory protein CYS3 of Neurospora crassa: nuclear localization, autogenous control, and regions required for transcriptional activation.
Molecular & general genetics : MGG 1993;239(3):334-44.
1992: Moien Kanaan; Y H Fu; George A Marzluf
The DNA-binding domain of the Cys-3 regulatory protein of Neurospora crassa is bipartite.
Biochemistry 1992;31(12):3197-203.
1991: Moien Kanaan; George A Marzluf
Mutational analysis of the DNA-binding domain of the CYS3 regulatory protein of Neurospora crassa.
Molecular and cellular biology 1991;11(9):4356-62.
1986: G B Olson; Moien Kanaan; L M Kelley; J F Jones
Specific allergen-induced Epstein-Barr nuclear antigen-positive B cells from patients with chronic-active Epstein-Barr virus infections.
The Journal of allergy and clinical immunology 1986;78(2):315-20.
1986: G B Olson; Moien Kanaan; G M Gersuk; L M Kelley; J F Jones
Correlation between allergy and persistent Epstein-Barr virus infections in chronic-active Epstein-Barr virus-infected patients.
The Journal of allergy and clinical immunology 1986;78(2):308-14.