Concepedia

Author

Yusnita Yakob

Institute for Medical ResearchORCID

Also Known As

Y Yakob, Y. Yakob, Yusnita Yakob

38

Publications

250

Citations

10

H-Index

17

Concepts

All Affiliations

Institute for Medical ResearchHospital Kuala LumpurMinistry of Health
YY

About

Yusnita Yakob is an author at Institute for Medical Research specializing in medicine, molecular biology, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

53

2

Molecular Biology

2

2

36

3

Natural Sciences

1

1

18

4

Biochemistry

1

1

18

5

Metabolism

1

1

18

Yusnita Yakob

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10

Publications

202

Citations

10

H-Index

YearCitations

Methanolic Extract of<i>Clinacanthus nutans</i>Exerts Antinociceptive Activity via the Opioid/Nitric Oxide‐Mediated, but cGMP‐Independent, Pathways

Mohammad Hafiz Abdul Rahim, Zainul Amiruddin Zakaria, Mohd Hijaz Mohd Sani,

Evidence-based Complementary and Alternative Medicine

2016

41

Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.

Mohd Khairul Nizam Mohd Khalid, Yusnita Yakob, Rohani Md Yasin,

PubMed

2015

25

Fructose-1,6-bisphosphatase deficiency as a cause of recurrent hypoglycemia and metabolic acidosis: Clinical and molecular findings in Malaysian patients

Lip Hen Moey, Nor Azimah Abdul Azize, Yusnita Yakob,

Pediatrics & Neonatology

2017

23

Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study

Huey Yin Leong, Nor Azimah Abdul Azize, Hui Bein Chew,

Orphanet Journal of Rare Diseases

2019

21

Carbamoylphosphate synthetase 1 (CPS1) deficiency: clinical, biochemical, and molecular characterization in Malaysian patients

Ernie Zuraida Ali, Mohd Khairul Nizam Mohd Khalid, Zabedah Md Yunus,

European Journal of Pediatrics

2015

18

Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes

Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel,

Molecular Genetics and Metabolism

2023

18

Adrenal insufficiency in a child with MELAS syndrome

Bushra Afroze, Nida Amjad, Shahnaz Ibrahim,

Brain and Development

2014

17

Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population

M. Mardhiah, Nor Azimah Abdul Azize, Yusnita Yakob,

Molecular Genetics and Metabolism Reports

2019

14

Clinical and Mutational Analysis of the<i>GCDH</i>Gene in Malaysian Patients with Glutaric Aciduria Type 1

Siti Aishah Abdul Wahab, Yusnita Yakob, Nor Azimah Abdul Azize,

BioMed Research International

2016

13

Novel mutations associated with carnitine-acylcarnitine translocase and carnitine palmitoyl transferase 2 deficiencies in Malaysia

Anasufiza Habib, Nor Azimah Abdul Azize, Salina Abd Rahman,

Clinical Biochemistry

2021

12

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