Asian Biomedicine

Editorial

Mini review

Uneingeschränkter Zugang | 01. Aug. 2023

Central resources of variant discovery and annotation and its role in precision medicine

Hashim Halim-Fikri

Hashim Halim-Fikri

Malaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains MalaysiaMalaysia

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Halim-Fikri, Hashim

, 

Sharifah-Nany Rahayu-Karmilla Syed-Hassan

Sharifah-Nany Rahayu-Karmilla Syed-Hassan

Malaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains MalaysiaMalaysia

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Syed-Hassan, Sharifah-Nany Rahayu-Karmilla

, 

Wan-Khairunnisa Wan-Juhari

Wan-Khairunnisa Wan-Juhari

• Malaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains MalaysiaMalaysia
• Human Genome Centre, School of Medical Sciences, Universiti Sains MalaysiaMalaysia

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Wan-Juhari, Wan-Khairunnisa

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Mat Ghani Siti Nor Assyuhada

Mat Ghani Siti Nor Assyuhada

Malaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains MalaysiaMalaysia

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Assyuhada, Mat Ghani Siti Nor

, 

Yetti Hernaningsih

Yetti Hernaningsih

Department of Clinical Pathology, Faculty of Medicine Universitas Airlangga, Dr. Soetomo Academic General HospitalSurabaya, Indonesia

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Hernaningsih, Yetti

, 

Narazah Mohd Yusoff

Narazah Mohd Yusoff

• Department of Clinical Pathology, Faculty of Medicine Universitas Airlangga, Dr. Soetomo Academic General HospitalSurabaya, Indonesia
• Clinical Diagnostic Laboratory, Advanced Medical and Dental Institute, Universiti Sains MalaysiaMalaysia

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Yusoff, Narazah Mohd

, 

Amir Feisal Merican

Amir Feisal Merican

• Institute of Biological Sciences, Faculty of Science, University of MalayaKuala Lumpur, Malaysia
• Center of Research for Computational Sciences and Informatics in Biology, Bio Industry, Environment, Agriculture and Healthcare (CRYSTAL), University of MalayaKuala Lumpur, Malaysia

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Merican, Amir Feisal

 und 

Bin Alwi Zilfalil

Bin Alwi Zilfalil

• Malaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains MalaysiaMalaysia
• Human Genome Centre, School of Medical Sciences, Universiti Sains MalaysiaMalaysia

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Zilfalil, Bin Alwi

  

Original article

Uneingeschränkter Zugang | 01. Aug. 2023

Burden of congenital and hereditary anomalies in the war-affected territory at Pakistan–Afghanistan border

Muhammad Naeem

Muhammad Naeem

Human Genetics Program, Department of Zoology, Faculty of Biological Sciences, Quaid-i-Azam UniversityIslamabad, Pakistan

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Naeem, Muhammad

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Bashir Ahmad

Bashir Ahmad

Human Genetics Program, Department of Zoology, Faculty of Biological Sciences, Quaid-i-Azam UniversityIslamabad, Pakistan

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Ahmad, Bashir

 und 

Sajid Malik

Sajid Malik

Human Genetics Program, Department of Zoology, Faculty of Biological Sciences, Quaid-i-Azam UniversityIslamabad, Pakistan

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Malik, Sajid

  

Brief communication (original)

Uneingeschränkter Zugang | 01. Aug. 2023

Risk factors of transient tachypnea of the newborn developing into pulmonary hypertension of the newborn: a case-control study

Gunlawadee Maneenil

Gunlawadee Maneenil

Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Prince of Songkla UniversitySongkhla, Thailand

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Maneenil, Gunlawadee

, 

Waricha Janjindamai

Waricha Janjindamai

Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Prince of Songkla UniversitySongkhla, Thailand

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Janjindamai, Waricha

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Supaporn Dissaneevate

Supaporn Dissaneevate

Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Prince of Songkla UniversitySongkhla, Thailand

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Dissaneevate, Supaporn

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Anucha Thatrimontrichai

Anucha Thatrimontrichai

Division of Neonatology, Department of Pediatrics, Faculty of Medicine, Prince of Songkla UniversitySongkhla, Thailand

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Thatrimontrichai, Anucha

  

Clinical vignettes

Uneingeschränkter Zugang | 01. Aug. 2023

Use of expanded carrier screening for retrospective diagnosis of two deceased siblings with Van Maldergem syndrome 2: case report

Nasim Rahmani

Nasim Rahmani

Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical SciencesTehran, Iran

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Rahmani, Nasim

, 

Mohammad Ahmadvand

Mohammad Ahmadvand

Department of Oncology and Stem Cell Transplantation, Shariati Hospital, School of Medicine, Tehran University of Medical SciencesTehran, Iran

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Ahmadvand, Mohammad

 und 

Golnaz Khakpour

Golnaz Khakpour

• Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical SciencesTehran, Iran
• Department of Eye Research Center, The Five Senses Institute, Rassoul Akram Hospital, School of Medicine, Iran University of Medical SciencesTehran, Iran

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Khakpour, Golnaz