Laksshman Sundaram

Illumina (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index1.8kcitations33works19.22yr avg
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Research Topics

Single-cell and spatial transcriptomics(14), Congenital heart defects research(10), Cancer Genomics and Diagnostics(9), Genomics and Rare Diseases(7), Genomics and Chromatin Dynamics(5)

Publications31 total

Correction: De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies
Human Genomics·2025Open Access
Predicting expression-altering promoter mutations with deep learning
Science·2025· 20 cited
Three-dimensional genome landscape of primary human cancers
Nature Genetics·2025· 7 citedOpen Access
Abstract 5046: Three-dimensional genome landscape of primary human cancers
Cancer Research·2025
Single-cell chromatin accessibility reveals malignant regulatory programs in primary human cancers
Science·2024· 34 citedOpen Access
Identification of constrained sequence elements across 239 primate genomes
Nature·2023· 96 citedOpen Access
Deep learning the cis-regulatory code of chromatin dynamics during cellular reprogramming
2023· 39 citedOpen Access
Single-cell analysis of open chromatin landscapes across diverse cancer types - Supplemental Files
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Single-cell analysis of open chromatin landscapes across diverse cancer types - Supplemental Files
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Single-cell analysis of open chromatin landscapes across diverse cancer types
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Single-cell analysis of open chromatin landscapes across diverse cancer types
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Single-cell analysis of open chromatin landscapes across diverse cancer types
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
The landscape of tolerated genetic variation in humans and primates
Science·2023· 158 citedOpen Access
The landscape of tolerated genetic variation in humans and primates
2023· 22 citedOpen Access
Stepwise Generation of Human Induced Pluripotent Stem Cell–Derived Cardiac Pericytes to Model Coronary Microvascular Dysfunction
Circulation·2023· 14 citedOpen Access
Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease (Invitro ArchR Object)
2023Open Access
Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease (Invivo ArchR Object)
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease (Invivo ArchR Object)
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease (Invitro ArchR Object)
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease
Cell·2022· 95 citedOpen Access
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Frequent Co-authors

Kyle Kai‐How Farh(11), Anshul Kundaje(7), William J. Greenleaf(7), Ioannis Karakikes(7), Hong Gao(5), Jeremy F. McRae(5), Howard Y. Chang(5), Ke Wang(5), Jinbo Xu(4), Serafim Batzoglou(4), Anna Shcherbina(4), François Aguet(4), Mohamed Ameen(4), Nirmal Vadgama(4), Xiaolin Li(3), Joshua G. Schraiber(3), Petko Fiziev(3), Lukas F. K. Kuderna(3), Mareike C. Janiak(3), Martin Kuhlwilm(3)