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1

Introducing clinical ethics consultation service in Malaysia: A SWOT analysis

Khoo, Erwin Jiayuan, Chua, Siew Houy, Thong, Meow-Keong, Zilfalil, Bin Alwi, Lantos, John

Журнал:

Clinical Ethics

Рік:

2019

Мова:

english

Файл:

PDF, 247 KB

english, 2019

2

Molecular Description of Familial DefectiveAPOB-100in Malaysia

Alyaa R. Al-Khateeb, Mohd Sapawi Mohd, Zukarnai Yusof, Bin Alwi Zilfalil

Журнал:

Biochemical Genetics

Рік:

2013

Мова:

english

Файл:

PDF, 374 KB

english, 2013

3

Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate

Iman Salahshourifar, Ahmad Sukari Halim, Wan Azman Wan Sulaiman, Bin Alwi Zilfalil

Журнал:

American Journal of Medical Genetics Part A

Рік:

2010

Мова:

english

Файл:

PDF, 72 KB

english, 2010

4

Contribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population

Iman Salahshourifar, Wan Azman Wan Sulaiman, Bin Alwi Zilfalil, Ahmad Sukari Halim

Журнал:

American Journal of Medical Genetics Part A

Рік:

2011

Мова:

english

Файл:

PDF, 249 KB

english, 2011

5

A simple and rapid genotyping method for beta-2 receptor (β2 AR) gene using allele specific multiplex PCR

S. M. N. Romaino, L. K. Teh, B. A. Zilfalil, C. P. Thong, A. A. Ismail, J. Amir, M. Z. Salleh, A. R. Noor, R. Ismail

Журнал:

Journal of Clinical Pharmacy and Therapeutics

Рік:

2004

Мова:

english

Файл:

PDF, 105 KB

english, 2004

6

Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia

Alyaa Al-Khateeb, Mohd K Zahri, Mohd S Mohamed, Teguh H Sasongko, Suhairi Ibrahim, Zurkurnai Yusof, Bin A Zilfalil

Журнал:

BMC Medical Genetics

Рік:

2011

Мова:

english

Файл:

PDF, 661 KB

english, 2011

7

Clinical manifestations in trisomy 9

T. P. Kannan, S. Hemlatha, R. Ankathil, B. A. Zilfalil

Журнал:

Indian Journal of Pediatrics

Рік:

2009

Мова:

english

Файл:

PDF, 138 KB

english, 2009

8

Genetic polymorphism of CYP2D6 in patients with cardiovascular disease – a cohort study

L. K. Teh, B. A. Zilfalil, I. Marina, B. S. Rosemi, R. Ismail

Журнал:

Journal of Clinical Pharmacy and Therapeutics

Рік:

2004

Мова:

english

Файл:

PDF, 82 KB

english, 2004

9

An improved rapid genotyping method for the study of beta-2 adrenergic receptor gene polymorphisms using single tube allele specific multiplex PCR

B. A. Zilfalil, B. P. Hoh, M. Z. Nizam, A. T. Liza-Sharmini, L. K. Teh, R. Ismail

Журнал:

Journal of Clinical Pharmacy and Therapeutics

Рік:

2006

Мова:

english

Файл:

PDF, 490 KB

english, 2006

10

Prevalence and molecular study of G6PD deficiency in Malaysian Orang Asli

F. Amini, E. Ismail, B-A. Zilfalil

Журнал:

Internal Medicine Journal

Рік:

2011

Мова:

english

Файл:

PDF, 90 KB

english, 2011

11

Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy

Mohd Shamshudin Watihayati, Hayati Fatemeh, Marzuki Marini, Amin Baig Atif, Wan Mohd Zahiruddin, Teguh Haryo Sasongko, Thean Hock Tang, ZAMH Zabidi-Hussin, Hisahide Nishio, Bin Alwi Zilfalil

Журнал:

Brain and Development

Рік:

2009

Мова:

english

Файл:

PDF, 96 KB

english, 2009

12

Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder

Teguh Haryo Sasongko, Gunadi, Surini Yusoff, Amin Baig Atif, Hayati Fatemeh, Abdulqawee Rani, Marzuki Marini, Che Badariah Ab Aziz, ZAMH Zabidi-Hussin, Hisahide Nishio, Bin Alwi Zilfalil

Журнал:

Brain and Development

Рік:

2010

Мова:

english

Файл:

PDF, 153 KB

english, 2010

13

Mutation screening of IRF6 among families with non-syndromic oral clefts and identification of two novel variants: Review of the literature

Iman Salahshourifar, Wan Azman Wan Sulaiman, Ahmad Sukari Halim, Bin Alwi Zilfalil

Журнал:

European Journal of Medical Genetics

Рік:

2012

Мова:

english

Файл:

PDF, 135 KB

english, 2012

14

Two closely spaced nonsense mutations in the DMD gene in a Malaysian family

Abdul Qawee Rani, Rusdy Ghazali Malueka, Teguh Haryo Sasongko, Hiroyuki Awano, Tomoko Lee, Mariko Yagi, Bin Alwi Zilfalil, A.B. Razak Salmi, Yasuhiro Takeshima, Z.A.M.H. Zabidi-Hussin, Masafumi Matsuo

Журнал:

Molecular Genetics and Metabolism

Рік:

2011

Мова:

english

Файл:

PDF, 126 KB

english, 2011

15

Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss

Siti Aishah Zainal, Mohd Khairi Md Daud, Normastura Abd Rahman, Zafarina Zainuddin, Zilfalil Alwi

Журнал:

International Journal of Pediatric Otorhinolaryngology

Рік:

2012

Мова:

english

Файл:

PDF, 191 KB

english, 2012

16

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization

M.N. Natasya Naili, C.H. Hasnita, A.K. Shamim, J. Hasnan, M.I. Fauziah, M.Y. Narazah, A. James, S. Zulkiflee, M.M.T. Nidzam, B.A. Zilfalil

Журнал:

Cancer Genetics and Cytogenetics

Рік:

2010

Мова:

english

Файл:

PDF, 341 KB

english, 2010

17

Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy

Rani, Abdul Qawee, Sasongko, Teguh Haryo, Sulong, Sarina, Bunyan, David, Salmi, Abdul Razak, Zilfalil, Bin Alwi, Matsuo, Masafumi, Zabidi-Hussin, Z. A. M. H.

Журнал:

Journal of Neurogenetics

Рік:

2013

Мова:

english

Файл:

PDF, 132 KB

english, 2013

18

A New Method for FMR1 Gene Methylation Screening by Multiplex Methylation-Specific Real-Time Polymerase Chain Reaction

Elias, Marjanu Hikmah, Ankathil, Ravindran, Salmi, Abdul Razak, Sudhikaran, Wanna, Limprasert, Pornprot, Zilfalil, Bin Alwi

Журнал:

Genetic Testing and Molecular Biomarkers

Рік:

2011

Мова:

english

Файл:

PDF, 363 KB

english, 2011

19

Towards understanding the low prevalence of Helicobacter pylori in Malays: Genetic variants among Helicobacter pylori -negative ethnic Malays in the north-eastern region of Peninsular Malaysia and Han Chinese and South Indians

Maran, Sathiya, Lee, Yeong Yeh, Xu, Shu Hua, Raj, Mahendra Sundramoorthy, Abdul Majid, Noorizan, Choo, Keng Ee, Zilfalil, Bin Alwi, Graham, David Y.

Журнал:

Journal of Digestive Diseases

Рік:

2013

Мова:

english

Файл:

PDF, 165 KB

english, 2013

20

Novel complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia

Mohseni, Jafar, Boon Hock, Chia, Abdul Razak, Che, Othman, Syah Nor Iman, Hayati, Fatemeh, PeiTee, Winnie Ong, Haniffa, Muzhirah, Zilfalil, Bin Alwi, Mohd. Rawi, Rowani, Ngu, Lock-Hock, Sasongko, Tegu

Журнал:

Рік:

2014

Мова:

english

Файл:

PDF, 872 KB

english, 2014

21

RB pocket domain B mutation frequency in Malaysia

Ishak, Siti-Raihan, Hanafi, Hanani, Alagaratnam, Joseph Vijaya, Zilfalil, Bin Alwi, Tajudin, Liza-Sharmini Ahmad

Журнал:

Ophthalmic Genetics

Рік:

2010

Мова:

english

Файл:

PDF, 594 KB

english, 2010

22

Deletion Analysis of SMN1 Exon 7 Alone May Be Necessary and Sufficient for the Diagnosis of Spinal Muscular Atrophy

Sasongko, Teguh Haryo, Gunadi,, Zilfalil, Bin Alwi, Zabidi-Hussin, ZAMH

Журнал:

Journal of Neurogenetics

Рік:

2011

Мова:

english

Файл:

PDF, 95 KB

english, 2011

23

Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population

Salahshourifar, Iman, Halim, Ahmad Sukari, Wan Sulaiman, Wan Azman, Zilfalil, Bin Alwi

Журнал:

Journal of Human Genetics

Рік:

2011

Мова:

english

Файл:

PDF, 243 KB

english, 2011

24

A genome wide pattern of population structure and admixture in peninsular Malaysia Malays

Hatin, Wan, Nur-Shafawati, Ab, Etemad, Ali, Jin, Wenfei, Qin, Pengfei, Xu, Shuhua, Jin, Li, Tan, Soon-Guan, Limprasert, Pornprot, Feisal, Merican, Rizman-Idid, Mohammed, Zilfalil, Bin

Журнал:

The HUGO Journal

Рік:

2014

Мова:

english

Файл:

PDF, 2.11 MB

english, 2014

25

De Novo Interstitial Deletion of 1q32.2–q32.3 Including the Entire IRF6 Gene in a Patient with Oral Cleft and Other Dysmorphic Features

Salahshourifar, I., Halim, A.S., Sulaiman, W.A.W., Ariffin, R., Naili Muhamad Nor, N., Zilfalil, B.A.

Журнал:

Cytogenetic and Genome Research

Рік:

2011

Мова:

english

Файл:

PDF, 320 KB

english, 2011

26

A Polymorphic Mutation, c.-3279T>G, in the UGT1A1 Promoter Is a Risk Factor for Neonatal Jaundice in the Malay Population

Yusoff, Surini, Takeuchi, Atsuko, Ashi, Chitose, Tsukada, Masako, Ma'Amor, Nur H, Zilfalil, Bin A, Yusoff, Narazah M, Nakamura, Tsutomu, Hirai, Midori, Harahap, Indra S K, Lee, Myeong J, Nishimura, No

Журнал:

Pediatric Research

Рік:

2010

Мова:

english

Файл:

PDF, 563 KB

english, 2010

27

Contribution of 6p24 to Non-syndromic Cleft Lip and Palate in a Malay Population: Association of Variants in OFC1

Salahshourifar, I., Halim, A. S., Sulaiman, W. A. W., Zilfalil, B. A.

Журнал:

Journal of Dental Research

Рік:

2011

Мова:

english

Файл:

PDF, 179 KB

english, 2011

28

Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography

Aishah, Z Siti, Khairi, M D Mohd, Normastura, A R, Zafarina, Z, Zilfalil, B A

Журнал:

Journal of Laryngology & Otology

Рік:

2008

Мова:

english

Файл:

PDF, 141 KB

english, 2008

29

Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies

Hoh, Boon-Peng, Deng, Lian, Julia-Ashazila, Mat Jusoh, Zuraihan, Zakaria, Nur-Hasnah, Ma’amor, Nur‐Shafawati, Ab Rajab, Hatin, Wan Isa, Endom, Ismail, Zilfalil, Bin Alwi, Khalid, Yusoff, Xu, Shuhua

Журнал:

Рік:

2015

Мова:

english

Файл:

PDF, 1.16 MB

english, 2015

30

Harmonizing the interpretation of genetic variants across the world: the Malaysian experience

Nik Hassan, Nik Norliza, Plazzer, John-Paul, Smith, Timothy D., Halim-Fikri, Hashim, Macrae, Finlay, Zubaidi AL, A., Zilfalil, Bin Alwi

Журнал:

BMC Research Notes

Рік:

2016

Мова:

english

Файл:

PDF, 830 KB

english, 2016

31

Transforming Growth Factor- α and Nonsyndromic Cleft Lip With or Without Palate or Cleft Palate Only in Kelantan, Malaysia

Rahman, Roselinda Abdul, Ahmad, Azlina, Rahman, Zainal Ariff Abdul, Mokhtar, Khairani Idah, Lah, Nik Ahmad Shah Nik, Zilfalil, Bin Alwi, Samsudin, Ab Rani

Журнал:

The Cleft Palate-Craniofacial Journal

Рік:

2008

Мова:

english

Файл:

PDF, 222 KB

english, 2008

32

Dissecting the genetic structure and admixture of four geographical Malay populations

Deng, Lian, Hoh, Boon-Peng, Lu, Dongsheng, Saw, Woei-Yuh, Twee-Hee Ong, Rick, Kasturiratne, Anuradhani, Janaka de Silva, H., Zilfalil, Bin Alwi, Kato, Norihiro, Wickremasinghe, Ananda R., Teo, Yik-Yin

Журнал:

Scientific Reports

Рік:

2015

Мова:

english

Файл:

PDF, 926 KB

english, 2015

33

The influence of angiotensin-converting enzyme gene ID polymorphism on human physical fitness performance in European and other populations

Li, Xiao, Ooi, Foong Kiew, Zilfalil, Bin Alwi, Yusoff, Surini

Журнал:

Sport Sciences for Health

Рік:

2016

Мова:

english

Файл:

PDF, 443 KB

english, 2016

34

Analysis of the genetic structure of the Malay population: Ancestry-informative marker SNPs in the Malay of Peninsular Malaysia

Yahya, Padillah, Sulong, Sarina, Harun, Azian, Wan Isa, Hatin, Ab Rajab, Nur-Shafawati, Wangkumhang, Pongsakorn, Wilantho, Alisa, Ngamphiw, Chumpol, Tongsima, Sissades, Alwi, Zilfalil

Журнал:

Forensic Science International: Genetics

Рік:

2017

Мова:

english

Файл:

PDF, 1021 KB

english, 2017

35

Population Genetic Structure of Peninsular Malaysia Malay Sub-Ethnic Groups

Hatin, Wan Isa, Nur-Shafawati, Ab Rajab, Zahri, Mohd-Khairi, Xu, Shuhua, Jin, Li, Tan, Soon-Guan, Rizman-Idid, Mohammed, Zilfalil, Bin Alwi, Harpending, Henry

Журнал:

Рік:

2011

Мова:

english

Файл:

PDF, 145 KB

english, 2011

36

Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy

Mohd Hussin, ZabidiAzhar, Sasongko, TeguhH, Salmi, AbdRazak, Zilfalil, BinAlwi, Albar, MohammedAli

Журнал:

Annals of Saudi Medicine

Рік:

2010

Мова:

english

Файл:

PDF, 594 KB

english, 2010

37

Introducing clinical ethics consultation service in Malaysia: A SWOT analysis

Khoo, Erwin Jiayuan, Chua, Siew Houy, Thong, Meow-Keong, Zilfalil, Bin Alwi, Lantos, John

Журнал:

Clinical Ethics

Рік:

2019

Файл:

PDF, 247 KB

2019

38

Relative proteome quantification of alpha, beta, gamma and delta globin chains in early eluting peaks of Bio-Rad variant II® CE-HPLC of hemoglobin from healthy and beta-thalassemia subjects in Malaysia

Abdullah, Uday Younis Hussein, Ibrahim, Hishamshah M., Jassim, Haitham Muhammed, Salleh, Mohamad Zaki, Kek, Teh Lay, Fakhruzzaman bin Noorizhab, Mohd Nur, Zilfalil, Bin Alwi, Wilairat, Prapin, Fucharo

Журнал:

Biochemistry and Biophysics Reports

Рік:

2019

Файл:

PDF, 3.31 MB

2019

39

Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β-Thalassemias

Abdullah, Uday Y.H., Ibrahim, Hishamshah M., Mahmud, Noraesah B., Salleh, Mohamad Z., Kek, Teh L., Noorizhab, Mohd N.F.B., Jassim, Haitham M., Othman, Iekhsan, Zainal Abidin, Syafiq A., Zilfalil, Bin

Журнал:

Рік:

2019

Мова:

english

Файл:

PDF, 1003 KB

english, 2019

40

Molecular analysis of promoter region of the SMN2 gene in the patients of spinal musculatr atrophy.

Baig, Atif, Shamsudin, Watihayati, Marzuki, Marini, Hayati, Fatemeh, Suriano, Teguh, Yean, Chan, Manicam, Ravichandran, Alwi, Zilfalil

Журнал:

Bioentrepreneur

Рік:

2010

Мова:

english

Файл:

PDF, 5.05 MB

english, 2010

41

Molecular analysis of promoter region of the SMN2 gene in the patients of spinal musculatr atrophy.

Baig, Atif, Shamsudin, Watihayati, Marzuki, Marini, Hayati, Fatemeh, Suriano, Teguh, Yean, Chan, Manicam, Ravichandran, Alwi, Zilfalil

Журнал:

Bioentrepreneur

Рік:

2010

Файл:

PDF, 5.05 MB

2010

42

Ancestry-informative marker (AIM) SNP panel for the Malay population

Yahya, Padillah, Sulong, Sarina, Harun, Azian, Wangkumhang, Pongsakorn, Wilantho, Alisa, Ngamphiw, Chumpol, Tongsima, Sissades, Zilfalil, Bin Alwi

Журнал:

International Journal of Legal Medicine

Рік:

2019

Мова:

english

Файл:

PDF, 2.94 MB

english, 2019

43

Ancestry-informative marker (AIM) SNP panel for the Malay population

Yahya, Padillah, Sulong, Sarina, Harun, Azian, Wangkumhang, Pongsakorn, Wilantho, Alisa, Ngamphiw, Chumpol, Tongsima, Sissades, Zilfalil, Bin Alwi

Журнал:

International Journal of Legal Medicine

Рік:

2019

Файл:

PDF, 2.94 MB

2019

44

Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience

Abdullah, Uday Younis Hussein, Simbak, Nordin, Azzubaidi, Marwan Saad, Osman, Raudhawati, Ibrahim, Hishamshah M., Jassim, Haitham Muhammed, Yunus, Noraini Mat, Johan, Muhammad Farid, Alwi, Zilfalil Bi

Журнал:

Journal of Hematopathology

Рік:

2020

Файл:

PDF, 604 KB

2020

45

Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity

Azman, Nurul Fatihah, Abdullah, Wan Zaidah, Hanafi, Sarifah, Diana, R., Bahar, Rosnah, Johan, Muhammad Farid, Zilfalil, Bin Alwi, Hassan, Rosline

Журнал:

Annals of Hematology

Рік:

2020

Мова:

english

Файл:

PDF, 344 KB

english, 2020

46

Global Globin 2020 Challenge: The Past, Present and Future

Zilfalil, Bin Alwi

Журнал:

Рік:

2019

Мова:

english

Файл:

PDF, 483 KB

english, 2019

47

Factors affecting health-related quality of life and its association with the Xmn1-GÎ³ polymorphism among adolescents with transfusion-dependent beta thalassemia and HbE/Beta thalassemia in East Coast Malaysia

Yusof, Wardah, Zulkifli, Maryam Mohd, Azman, Nurul Fatihah, Ab Hamid, Siti Azrin, Othman, Azizah, Draman, Nani, Zilfalil, Bin Alwi, Hassan, Rosline, Abdullah, Wan Zaidah

Журнал:

Pediatric Hematology Oncology Journal

Рік:

2020

Файл:

PDF, 3.45 MB

2020

48

Genotype-Phenotype Correlation of Î²-Thalassemia in Malaysian Population: Toward Effective Genetic Counseling

Abdullah, Uday Y. H., Ibrahim, Hishamshah M., Mahmud, Noraesah Binti, Salleh, Mohamad Zaki, Teh, Lay Kek, Noorizhab, Mohd Nur Fakhruzzaman bin, Zilfalil, Bin Alwi, Jassim, Haitham Muhammed, Wilairat,

Журнал:

Рік:

2020

Файл:

PDF, 1.17 MB

2020

49

The ITHANET-Human Variome Project: Moving Functional Annotation Forward

Kountouris, Petros, Stephanou, Coralea, Lederer, Carsten W., Tamana, Stella, Minaidou, Anna, Xenophontos, Maria, Angastiniotis, Michael, Eleftheriou, Androulla, Zilfalil, Bin Alwi, Ramesar, Raj S., El

Журнал:

Рік:

2019

Файл:

PDF, 598 KB

2019