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11
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )
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Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )

ALSMADI, Osama ; MEYER, Brian F ; ALKURAYA, Fowzan ; WAKIL, Salma ; ALKAYAL, Fadi ; AL-SAUD, Haya ; RAMZAN, Khushnooda ; AL-SAYED, Moeenaldeen

European journal of human genetics : EJHG, 2009-01, Vol.17 (1), p.14-21 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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12
A study of PON1 as a susceptibility gene for hyperlipidaemia and onset of coronary artery disease
A study of PON1 as a susceptibility gene for hyperlipidaemia and onset of coronary artery disease
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A study of PON1 as a susceptibility gene for hyperlipidaemia and onset of coronary artery disease

Muiya, Paul ; Wakil, Salma ; Al‐Najai, Mohammed ; Vigilla, Mary Grace ; Andres, Editha ; Alshahid, Maie ; Dzimiri, Nduna

The FASEB journal, 2010-04, Vol.24 (S1), p.lb121-lb121 [Periódico revisado por pares]

Federation of American Societies for Experimental Biology

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13
The rs2228671C>T of the LDLR gene confers risk for low HDL and early onset of coronary artery disease
The rs2228671C>T of the LDLR gene confers risk for low HDL and early onset of coronary artery disease
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The rs2228671C>T of the LDLR gene confers risk for low HDL and early onset of coronary artery disease

Alrasheed, Maha M ; Muiya, Paul ; Wakil, Salma ; Al‐Najai, Mohammed ; Andres, Editha ; Mazher, Nejat ; Dzimiri, Nduna

The FASEB journal, 2010-04, Vol.24 (S1), p.lb134-lb134 [Periódico revisado por pares]

Federation of American Societies for Experimental Biology

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14
Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients
Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients
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Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients

Alsum, Zobaida ; Hawwari, Abbas ; Alsmadi, Osama ; Al-Hissi, Safa ; Borrero, Esteban ; Abu-staiteh, Asma’ ; Khalak, Hanif G. ; Wakil, Salma ; Eldali, Abdelmoneim M. ; Arnaout, Rand ; Al-ghonaium, Abdulaziz ; Al-Muhsen, Saleh ; Al-Dhekri, Hasan ; Al-Saud, Bandar ; Al-Mousa, Hamoud

Journal of clinical immunology, 2013, Vol.33 (1), p.55-67 [Periódico revisado por pares]

Boston: Springer US

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15
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family
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A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Wakil, Salma M ; Bohlega, Saeed ; Hagos, Samya ; Baz, Batoul ; Al Dossari, Haya ; Ramzan, Khushnooda ; Al-Hassnan, Zuhair N

European journal of medical genetics, 2013-01, Vol.56 (1), p.43-45 [Periódico revisado por pares]

Netherlands: Elsevier Masson SAS

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16
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
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New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3

Alshahid, Maie ; Wakil, Salma M ; Al-Najai, Mohammed ; Muiya, Nzioka P ; Elhawari, Samar ; Gueco, Daisy ; Andres, Editha ; Hagos, Samia ; Mazhar, Nejat ; Meyer, Brian F ; Dzimiri, Nduna

Human genomics, 2013-06, Vol.7 (1), p.15-15, Article 15 [Periódico revisado por pares]

England: BioMed Central

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17
Involvement of ATP-binding cassette, subfamily A polymorphism with susceptibility to coronary artery disease
Involvement of ATP-binding cassette, subfamily A polymorphism with susceptibility to coronary artery disease
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Involvement of ATP-binding cassette, subfamily A polymorphism with susceptibility to coronary artery disease

ZARGAR, SEEMA ; WAKIL, SALMA ; MOBEIREK, ABDUELAH F ; AL-JAFARI, ABDULAZIZ A

Biomedical reports, 2013-11, Vol.1 (6), p.883-888 [Periódico revisado por pares]

England: D.A. Spandidos

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18
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
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A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders

Muiya, Nzioka P ; Wakil, Salma M ; Tahir, Asma I ; Hagos, Samya ; Najai, Mohammed ; Gueco, Daisy ; Al-Tassan, Nada ; Andres, Editha ; Mazher, Nejat ; Meyer, Brian F ; Dzimiri, Nduna

Human genomics, 2013-12, Vol.7 (1), p.25-25, Article 25 [Periódico revisado por pares]

England: BioMed Central

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19
A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24
A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24
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A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24

Wakil, Salma M. ; Muiya, Nzioka P. ; Tahir, Asma I. ; Al-Najai, Mohammed ; Baz, Batoul ; Andres, Editha ; Mazhar, Nejat ; Al Tassan, Nada ; Alshahid, Maie ; Meyer, Brian F. ; Dzimiri, Nduna Letizia, Claudio

Disease markers, 2014-01, Vol.2014, p.291419-10 [Periódico revisado por pares]

United States: Hindawi Publishing Corporation

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20
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
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Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T

Wakil, Salma M. ; Ramzan, Khushnooda ; Abuthuraya, Rula ; Hagos, Samya ; Al-Dossari, Haya ; Al-Omar, Rana ; Murad, Hatem ; Chedrawi, Aziza ; Al-Hassnan, Zuhair N. ; Finsterer, Josef ; Bohlega, Saeed

Gene, 2014-02, Vol.536 (1), p.217-220 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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