رويده فايز المومني

• قسم العلوم الطبية المخبرية - عضو هيئة تدريس

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قسم العلوم الطبية المخبرية
rfalmomani7@just.edu.jo

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الدكـتوراة في علم الوراثه من جامعة ليدن, 2013
ماجستير في العلوم الحياتيه التطبيقيه من جامعة العلوم والتكنولوجيا الاردنيه, 2005
بكالوريوس في العلوم الحياتيه من جامعة مؤته, 2001

Publications

Almomani R, van der Stoep N, Bakker E, den Dunnen JT, Breuning MH, Ginjaar IB., "Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis.," Neuromuscul Disord., vol. 19, no. , pp. 383-390, 2009
Yu Sun,1,11 Rowida Almomani,1,11 Emmelien Aten,1 Jacopo Celli,1 , "Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA gene.," Am J Hum Genet, vol. 87, no. , pp. 146-53, 2010
Almomani R, van der Heijden J, Ariyurek Y, Lai Y, Bakker E, van Galen M, Breuning MH, den Dunnen JT., "Experiences with array-based sequence capture; toward clinical applications.," Eur J Hum Genet. , vol. , no. , pp. 0-0,
Santen GW, Aten E, Sun Y, Almomani R, Gilissen C, Nielsen M, Kant SG, Snoeck IN, Peeters EA, Hilhorst-Hofstee Y, Wessels MW, den Hollander NS, Ruivenkamp CA, van Ommen GJ, Breuning MH, den Dunnen JT, van Haeringen A, Kriek M., "Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.," Nature Genetics, vol. , no. , pp. 0-0,
Lemmers RJ1, Tawil R, Petek LM, Balog J, Block GJ, Santen GW, , "Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.," , vol. , no. , pp. 0-0,
Aten E, Sun Y, Almomani R, Santen GW, Messemaker T, Maas SM, Breuning MH, den Dunnen JT. , "Exome sequencing identifies a branch point variant in Aarskog-Scott syndrome.," Hum Muta, vol. , no. , pp. 0-0, 2013
Sun Y1, Almomani R, Breedveld GJ, Santen GW, Aten E, Lefeber DJ, &l, "Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).," Hum Muta, vol. , no. , pp. 0-0,
Almomani R, Sun Y, Aten E, Hilhorst-Hofstee Y, Peeters-Scholte CM, van Haeringen A, Hendriks YM, den Dunnen JT, Breuning MH, Kriek M, Santen GW., "GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North America.," Am J Med Genet A., vol. , no. , pp. 0-0,
Sikkema-Raddatz B, Johansson LF, de Boer EN, Almomani R, Boven LG, van den Berg MP, van Spaendonck-Zwarts KY, van Tintelen JP, Sijmons RH, Jongbloed JD, Sinke RJ., "Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnostics.," Hum Muta, vol. , no. , pp. 0-0,
van Spaendonck-Zwarts KY, Posafalvi A, van den Berg MP, Hilfiker-Kleiner D, Bollen IA, Sliwa K, Alders M, Almomani R, van Langen IM, van der Meer P, Sinke RJ, van der Velden J, Van Veldhuisen DJ, van Tintelen JP, Jongbloed JD, "Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.," Eur Heart J. , vol. , no. , pp. 0-0,
Almomani R, Verhagen JM, Herkert JC, Brosens E, van Spaendonck-Zwarts KY, Asimaki A, van der Zwaag PA, Frohn-Mulder IM, Bertoli-Avella AM, Boven LG, van Slegtenhorst MA, van der Smagt JJ, van IJcken WF, Timmer B, van Stuijvenberg M, Verdijk RM, Saffitz JE, du Plessis FA, Michels M, Hofstra RM, Sinke RJ, van Tintelen JP, Wessels MW, Jongbloed JD, van de Laar IM., "Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy.," J Am Coll Cardiol., vol. , no. , pp. 0-0,
Martinelli-Boneschi F, Colombi M, Castori M, Devigili G, Eleopra R, Malik RA, Ritelli M, Zoppi N, Dordoni C, Sorosina M, Grammatico P, Fadavi H, Gerrits MM, Almomani R, Faber CG, Merkies IS, Toniolo D; INGI Network, Cocca M, Doglioni C, Waxman SG, Dib-Hajj SD, Taiana MM, Sassone J, Lombardi R, Cazzato D, Zauli A, Santoro S, Marchi M, Lauria G., "COL6A5 variants in familial neuropathic chronic itch.," Brain, vol. , no. , pp. 0-0, 2017
Rowida Almomani, The use of new technology to improve genetic testing, ,
"COG6 Novel Variant: From Prenatal Diagnosis to Successful Preimplantation Genetic Testing", Biomedical and Biotechnology Research Journal

Mohammad Abdullah Saleem Al Shboul, Rowida Fayez Abdalla Al-Momani, Osamah Yousef Mahmoud Batiha

26/06/2026
"A Novel Variant in KCTD3 Gene in Patients with Global Developmental Delay, Seizures, and Cerebellar Hypoplasia", BIOMEDICAL AND BIOTECHNOLOGY RESEARCH JOURNAL

Rowida Fayez Abdalla Al-Momani, Mohammad Abdullah Saleem Al Shboul

27/03/2026
"Gene expression alterations in testicular biopsies from males with spermatogenesis arrest identified by transcriptome analysis", Plos one

Osamah Yousef Mahmoud Batiha, Esra'A Omar Mohammad Al-Zoubi, Rowida Fayez Abdalla Al-Momani

12/09/2025
"he Association Between the rs2200733 SNP and Atrial Fibrillation Among Arabs: A Study from Jordan", Biologics: Targets and Therapy

Abdullah Hamad Mustafa Al-Kasasbeh, Omar Falah Saeed Khabour, Rowida Fayez Abdalla Al-Momani, Muhannad Jowdat Hamad Ababneh, Rashid Khaled Muhsen Ibdah, Mohamad Ismail Salim Jarrah, Sukaina Ismael Faisal Rawashdeh, Abdelsamea Mohammed Abdulsamea Seif

17/12/2024
"Whole exome sequencing revealed ultra-rare genetic variations in juvenile myoclonic epilepsy", Neurological Sciences

Ansam Mansour Mohammad Yacoub, Amjad Abduallah Mousa Mahasneh, Ahmed Moh'D Abdel Latif Yassin, Rowida Fayez Abdalla Al-Momani, Suha Awwad Hasan Aqaileh, Abdel?Hameed Al?Mistarehi

30/11/2024
"Genetic Profiling of Sodium Channels in Diabetic Painful and Painless and Idiopathic Painful and Painless Neuropathies", International Journal of Molecular Sciences

Rowida Fayez Abdalla Al-Momani

05/05/2023
"Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy", International Journal of Molecular Sciences

Rowida Fayez Abdalla Al-Momani

15/11/2022
"Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy", International Journal of Molecular Sciences

Rowida Fayez Abdalla Al-Momani

23/06/2022
"Elevated Interleukin 31 serum levels in hemodialysis patients are associated with uremic pruritus", Cytokine

Ashraf Omar Khalil Oweis, Firas Ahmed Abdelgader Al-Qarqaz, Khaldon Ghazi Khaled Bodoor, Leen Hussein Ali Heis, Mahmoud A. M. Alfaqih, Rowida Fayez Abdalla Al-Momani, Motaz Abdullah Mitib Obeidat

07/11/2020
"Evaluation of molecular inversion probe versus TruSeq? custom methods for targeted next-generation sequencing", PLOS One

Rowida Fayez Abdalla Al-Momani

16/08/2020
"IL-33/13 Axis and IL-4/31 Axis Play Distinct Roles in In ? ammatory Process and Itch in Psoriasis and Atopic Dermatitis", Clinical, Cosmetic and Investigational Dermatology

Khaldon Ghazi Khaled Bodoor, Firas Ahmed Abdelgader Al-Qarqaz, Mahmoud A. M. Alfaqih, Leen Hussein Ali Heis, Ashraf Omar Khalil Oweis, Rowida Fayez Abdalla Al-Momani, Motaz Abdullah Mitib Obeidat

15/06/2020
"Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy", Journal of Medical Genetics

Rowida Fayez Abdalla Al-Momani

29/07/2019
"A gain-of-function sodium channel ?2-subunit mutation in painful diabetic neuropathy.", Molecular Pain

Rowida Fayez Abdalla Al-Momani

08/04/2019
"Basal cell carcinoma pathology requests and reports are lacking important information", Journal of Skin Cancer

Firas Ahmed Abdelgader Al-Qarqaz, Khaldon Ghazi Khaled Bodoor, Haytham Mahmoud Rashid Eloqayli, Wisam Ahmed Abdul Qadir Al-Gargaz, Diala Mahmoud Saleh Alshiyab, Jihan Mohammed Sulaiman Muhaidat, Mohammad Abdulhamid Abdalla Al-Qudah, Rowida Fayez Abdalla Al-Momani

25/12/2018
"Yield of peripheral sodium channels gene screening in pure small fibre neuropathy", Journal of Neurology, Neurosurgery, and Psychiatry

Rowida Fayez Abdalla Al-Momani

15/12/2018
"Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome", Circulation research

Rowida Fayez Abdalla Al-Momani

12/01/2018

Assistant Dean, Dean assistant, Sep 2021 - Sep 2022
Assistant Dean, Dean assistant, Sep 2020 - Sep 2021
Assistant Dean, Dean assistant, Sep 2019 - Sep 2020
Faculty Member, Department of Medical Laboratory Sciences, Mar 2017 - Present

ADVANCED CYTOGENETIC DIAGNOSTIC PRACTICAL TRAINING
ADVANCED DIAGNOSTIC IMMUNOHEMATOLOGY AND BLOOD BANKING PRACTICAL TRAINING
ADVANCED HUMAN CYTOGENETIC
ADVANCED HUMAN GENETICS
ADVANCED MOLECULAR BIOLOGY
ADVANCED MOLECULAR GENETICS PRACTICAL TRAINING
DIAGNOSTIC MOLECULAR BIOLOGY AND CYTOGENETIC
DIAGNOSTIC MOLECULAR BIOLOGY AND CYTOGENETIC PRACTICAL
MOLECULAR BIOLOGY
MOLECULAR DIAGNOSTIC AND CYTOGENETIC
MOLECULAR DIAGNOSTIC AND CYTOGENETIC( LAB)
MOLECULAR GENETICS
MOLECULAR TOXICOLOGY
SCIENTIFIC RESEARCH METHODS
SEMINAR
SPECIAL TOPICS IN HUMAN GENETICS

جامعة العلوم والتكنولوجيا الأردنية

ص.ب. 3030, إربد 22110, الأردن

+ 962 2-7201000 :هاتف أرضي
+ 962 2-7095123 :فاكس

البريد الإلكتروني: public@just.edu.jo