Author

Adam Nelson

Sydney Children's HospitalPrimary ORCID profile (0000-0002-3074-2713 · 3 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Adam NelsoniD3 papers · Brigham and Women's Hospital

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Adayapalam Nandini· 2 shared Andrew J. DeansiD· 2 shared Caitlin Harris· 2 shared Elissah GrangeriD· 2 shared Eunike VelleueriD· 2 shared Jordi SurrallésiD· 2 shared Lisa C. WorganiD· 2 shared Michael F. SharpiD· 2 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adayapalam Nandini

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3 papers

Recent·Most cited

Multi-lineage natural gene therapy mediated by embryonic triploid mosaicism in the context of Fanconi anaemia

Michael F. Sharp, Caitlin Harris, Chirantani Mukherjee, Stevan Novakovic, Elissah Granger, Roser M. Pujol, Gerard Muñoz‐Pujol, Elva Z. Shi, Karen A. Dun, Cesar Salinas‐La Rosa, Zhisheng Xu, Mark Domenic Pertile, Krystle Standen, Rebecca Walsh, Andrew J. Deans, , Wayne Crismani

A patient with Fanconi anemia developed triploid hematopoietic stem cells that lacked the disease phenotype, enabling sustained hematopoiesis through restored DNA repair.

medRxiv · Oct 29, 2025 · PreprintGenetic & Genomic Medicine

Analysis of BRCA1, BRCA2 and PALB2 related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes

Sharon E. Johnatty, Emma Tudini, Michael T. Parsons, Kyriaki Michailidou, Maria Zanti, Daffodil M. Canson, Aimee L. Davidson, Tamar R. Berger, Rasim Özgür Rosti, Christian Peter Kratz, Reinhard Kalb, Lisa J. McReynolds, Neelam Giri, Marcy E. Richardson, Tina F. Pesaran, , Amanda B. Spurdle

medRxiv · May 25, 2025 · PreprintGenetic & Genomic Medicine

Clinical and Genetic Spectrum of Fanconi Anaemia in Australia and New Zealand.

Hannah Fluhler, Elissah Granger, Michael F. Sharp, Caitlin Harris, Mark J. McKinley, Sarbjit Riyat, Christine Krieg, Andrew J. Deans, Chris Fraser, Siobhan F. Cross, Tina L. Carter, Lisa C. Worgan, Adam Nelson, Lucy C. Fox, Jillian K. Nicholl, , Wayne Crismani

This study investigates the clinical and genetic spectrum of Fanconi anaemia in Australia and New Zealand, finding a correlation between testing rates and case detection, and highlighting increased susceptibility to HNSCC.

medRxiv · Oct 21, 2024 · PreprintGenetic & Genomic Medicine