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Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource (www.nature.com)

Christopher Koch, Shareef Khalid, Maleeha Zaman Khan et al.

78 Authors
2026-06-17 Published
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CK
Christopher Koch
SK
Shareef Khalid
MZ
Maleeha Zaman Khan
SB
Shruthi Bandyadka
BD
Brian Doyon
DP
Daniel P. Denning
MJ
Muhammad Jahanzaib
MR
Muhammad Rehan Mian
WG
Wafa Gul
MB
Muhammad Bilal Liaqat
AB
Aneeqa Bano
MD
Marium Dahar
NS
Namra Saqib
LK
Lubna Kamani
NB
Nazish Butt
AJ
Anjum Jalal
RS
Riffat Sultana
SA
Shahid Abbas
MS
Musfireh Siddiqeh
MH
Muhammad Haroon
AK
Asadullah Khan
KP
Khalid Parvez Babar
AR
Aflak Rasheed
JI
Javed Iqbal
FA
Faizan Aslam
UU
Umar Usman
MA
Muhammad Akram Bajwa
AH
Ali Hyder
MS
Muhammad Sadik Memon
NH
Nauman Hashmani
MI
Mohsin Iqbal Haroon
AM
Ambreen Muddassir
SA
Syed Asif Raza Zaidi
MA
Mateen Akram
MH
Muhammad Hussain
SN
Saima Naz Mohsin
SB
Samreen Bugti
TM
Tariq Mehmood
AL
Abdul Lateef Rodeni
SM
Shahid Mukhtar
TR
Tahir Rasool
AM
Adil Mahmood
MN
Muhammad Noor Wazir
SJ
Sheraz Jamal Khan
MA
Muhammad Asghar Khan
RG
Rahmat Ghaffar
SJ
Sanaullah Jan
NU
Noor Ul Hadi
RA
Roshina Anjum
RA
Rehan Abdullah
MU
Muhammad Usman Musharraf
MT
Muhammad Tahir Bashir
MA
Muhammad Ali
IM
Irfan Majeed
MH
Muhammad Haroon Bilal
SA
Shahzad Ali Khan
CH
Chihiro Hata
IK
Ikuyo Kou
MA
Makoto Asaumi
WM
Wataru Morii
KR
Katherine R. Smith
KK
Kousik Kundu
KL
Kieren Lythgow
SM
Stewart MacArthur
SW
Sebastian Wasilewski
SP
Slavé Petrovski
RG
Regeneron Genetics Center
JL
Juan L. Rodriguez-Flores
MR
Moeen Riaz
MK
Manav Kapoor
JD
Joshua D. Backman
AR
Alan R. Shuldiner
JE
James E. Bradner
IS
Igor Splawski
AR
Asif Rasheed
JE
John E. Dominy
AM
Allan M. Gurtan
DS
Danish Saleheen
Chapter II

Abstract

Summary of the research findings

Naturally occurring loss-of-function variants in human genes enable drug target discovery because they mimic pharmacological inhibition of proteins. However, the study of these genetic variants is constrained by their rarity. Sequencing of diverse populations, particularly those enriched in familial relatedness, has been postulated to promote discovery of rare genetic variants. Here we present the Pakistan Genome Resource, a South Asian biobank with high familial relatedness comprising 173,303 participants, who collectively carry naturally occurring homozygous loss-of-function variants in 6,476 genes. We describe the genetic architecture of this population, associations between genes and biomarkers, the distribution of loss-of-function variants across molecular pathways, and recall-by-genotype studies of therapeutically relevant genes. The Pakistan Genome Resource expands the catalogue of human genetic variants, provides a comprehensive genetic reference resource for the Pakistani population, and demonstrates the value of studying diverse cohorts to advance human health.

Chapter III

AI-Generated Summary

AI-generated by DNAGENICS

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Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

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