Khalid Mahmood

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 19 papers. Top paper: “Germline MBD4 deficiency causes a multi-tumor predisposition syndrome”.

Germline MBD4 deficiency causes a multi-tumor predisposition syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.018

N/A

1.9DataRank · unranked

79 citations

Hannah D. West, Edward Chew, Sara Galavotti, Christoffer Flensburg, Judith E. Grolleman +64 more

Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

Genetics in Medicine(2023)10.1016/j.gim.2023.100992

N/A

1.0DataRank · unranked

33 citations

Xiaoyu Yin, Marcy E. Richardson, Marta Pineda, Andreas Laner, Deborah Ritter +27 more

Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival

medRxiv(2023)10.1101/2023.03.10.23287127

N/A

0.960DataRank · unranked

24 citations

Robert S. Steinfelder, Tabitha A. Harrison, Bernard J. Pope, Syed Hassan Ejaz Zaidi, Conghui Qu +57 more

Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

Nature Genetics(2023)10.1038/s41588-023-01305-1

N/A

0.654DataRank · unranked

77 citations

Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica Johnson +95 more

Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures

Nature Communications(2022)10.1038/s41467-022-30916-1

N/A

0.542DataRank · unranked

36 citations

Tabitha A. Harrison, Bernard J. Pope, Syed Hassan Ejaz Zaidi, Conghui Qu, Robert S. Steinfelder +47 more

Intratumoural pks Escherichia coli is associated with risk of metachronous colorectal cancer and adenoma development in people with Lynch syndrome

EBioMedicine(2025)10.1016/j.ebiom.2025.105661

N/A

0.360DataRank · unranked

10 citations

Peter Georgeson, Mark Clendenning, Khalid Mahmood, Romy Walker, Julia Como +17 more

DNA methylation signatures and the contribution of age-associated methylomic drift to carcinogenesis in early-onset colorectal cancer

medRxiv(2021)10.1101/2021.03.24.21254210

N/A

0.330DataRank · unranked

8 citations

Mark Clendenning, Ee Ming Wong, Christophe Rosty, Khalid Mahmood, Peter Georgeson +14 more

Elucidating the Risk of Colorectal Cancer for Variants in Hereditary Colorectal Cancer Genes

(2023)10.1053/j.gastro.2023.06.032

N/A

0.312DataRank · unranked

7 citations

Minta Thomas, Conghui Qu, Xiaoliang Wang, Jeroen R. Huyghe, Jihoon E. Joo +77 more

DNA Mismatch Repair Gene Mosaicism Is Rare in People With Mismatch Repair-Deficient Cancers

Gastroenterology(2025)10.1053/j.gastro.2024.12.027

N/A

0DataRank · unranked

1 citations

Jihoon E. Joo, Khalid Mahmood, Peter Georgeson, Mark Clendenning, Sharelle Joseland +15 more

Age-specific trends in colorectal, appendiceal, and anal tumour incidence by histological subtype in Australia from 1990 to 2020: a population-based time-series analysis

medRxiv(2025)10.1101/2025.04.21.25326138

N/A

0DataRank · unranked

1 citations

James G. Dowty, Khalid Mahmood, Finlay Macrae, Christophe Rosty, Daniel D. Buchanan +2 more

Germline and Tumor Sequencing as a Diagnostic Tool To Resolve Suspected Lynch Syndrome

Journal of Molecular Diagnostics(2020)10.1016/j.jmoldx.2020.12.003

N/A

0DataRank · unranked

24 citations

Mark Clendenning, Christophe Rosty, Khalid Mahmood, Peter Georgeson, Jihoon E. Joo +14 more

Age-specific trends in colorectal, appendiceal, and anal tumour incidence by histological subtype in Australia from 1990 to 2020: a population-based time-series analysis

The Lancet Regional Health - Western Pacific(2025)10.1016/j.lanwpc.2025.101728

N/A

0DataRank · unranked

0 citations

James G. Dowty, Khalid Mahmood, Finlay A. Macrae, Christophe Rosty, Daniel D. Buchanan +2 more

A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

Journal of Translational Medicine(2023)10.1186/s12967-023-04143-1

N/A

0DataRank · unranked

22 citations

Khalid Mahmood, Jihoon E. Joo, Mark Clendenning, Peter Georgeson, Julia Como +45 more

DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands

Cancers(2023)10.3390/cancers15204925

N/A

0DataRank · unranked

1 citations

Khalid Mahmood, Julia Como, Mark Clendenning, Jihoon E. Joo, Peter Georgeson +28 more

DNA mismatch repair gene variant classification: evaluating the utility of somatic mutations and mismatch repair deficient colonic crypts and endometrial glands

medRxiv(2023)10.1101/2023.09.26.23295173

N/A

0DataRank · unranked

1 citations

Khalid Mahmood, Julia Como, Mark Clendenning, Jihoon E. Joo, Peter Georgeson +29 more

Intratumoral presence of the genotoxic gut bacteria pks+ E. coli, Enterotoxigenic Bacteroides fragilis, and Fusobacterium nucleatum and their association with clinicopathological and molecular features of colorectal cancer

British Journal of Cancer(2024)10.1038/s41416-023-02554-x

N/A

0DataRank · unranked

74 citations

Yen Lin Chu, Peter Georgeson, Romy Walker, Khalid Mahmood, Mark Clendenning +20 more

Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.09.002

N/A

0DataRank · unranked

15 citations

Marcy E. Richardson, Andreas Laner, Xuemei Shi, Elisabet Ognedal, Valeria Vasta +27 more

Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylation

Familial Cancer(2025)10.1007/s10689-025-00456-w

N/A

0DataRank · unranked

3 citations

Khalid Mahmood, Mark Clendenning, Romy Walker, Peter Georgeson, Julia Como +5 more

Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications

Translational Oncology(2025)10.1016/j.tranon.2024.102266

N/A

0DataRank · unranked

6 citations

Jihoon E. Joo, Khalid Mahmood, Mark Clendenning, Julia Como, Susan Preston +25 more