All papers authored by John Joseph Reynolds
Refreshing results…
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Arash Algouneh,
Rehna Krishnan,
John J. Reynolds ,
Kevin C. J. Nixon,
Jun Hao,
Jihoon Lee,
Yue Feng,
Chehronai Fozil,
Mia Stanic,
Talya Yerlici,
Peiran Su,
Fraser Soares ,
Elisabeth Liedtke,
Gil Prive
and 7 other authors
Excessive transcription-replication conflicts are a vulnerability of BRCA1-mutant cancers
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John J. Reynolds ,
Farid Ullah,
Bertrand Isidor,
Robert F. Shearer ,
Xenia Latypova,
Ryan M. Baxley ,
Antony W. Oliver ,
Anil Ganesh,
Sophie L. Cooke ,
Satpal S. Jhujh ,
Gavin S. McNee,
Robert Hollingworth,
Martin R. Higgs ,
Toyoaki Natsume
and 33 other authors
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy
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Srijita Dhar,
Joshua A. Sommers ,
Arindam Datta,
Gabriel M. C. Longo ,
Laura J. Grange ,
John J. Reynolds ,
Sophie L. Cooke ,
Gavin S. McNee ,
Robert Hollingworth,
Beth L. Woodward ,
Anil N. Ganesh ,
Stephen J. Smerdon,
Claudia M. Nicolae
and 9 other authors
RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1
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Ryan C. James,
Durga Pokharel,
Yongqing Zhang,
John J. Reynolds ,
Gavin S. McNee,
Andrew P. Jackson ,
Grant S. Stewart ,
Michael M. Seidman
Download from www.nature.com
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John J. Reynolds ,
Grant S. Stewart,
Bernd Wollnik,
Gökhan Yigit,
Keith W. Caldecott
Novel PNKP mutations causing defective DNA strand break repair and PARP1 hyperactivity in MCSZ
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Nissan Vida Baratang,
Jennifer B. Phillips,
Jeremy Wegner,
Ashley McFarquhar,
Martin R. Higgs,
Audrey E. Christiansen,
Denise G. Lanza,
John R. Seavitt,
Mahim Jain,
Xiaohui Li,
David A. Parry,
Vandana Raman,
David Chitayat
and 237 other authors
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Marianne van Koegelenberg,
Matthew E. Hurles,
Angela F. Brady,
Andrew P. Jackson,
Grant S. Stewart ,
Noel F. Lowndes
Analysis of novel missense ATR mutations reveals new splicing defects underlying Seckel Syndrome
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A. Bacon,
U. Mallick,
A. Hackshaw,
J. C. Watkinson,
K. Boelaert,
A. S. Turnell,
V. E. Smith
and 1 other authors
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Joaquin Herrero-Ruiz,
Tiago M. Bandeiras,
Pedro M. Matias ,
Sarah L. Maslen,
J. Mark Skehel,
Grant S. Stewart ,
Clare C. Davies
Download from www.ncbi.nlm.nih.gov
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Louise S. Bicknell,
Paula Carroll,
Martin R. Higgs,
Ranad Shaheen,
Jennie E. Murray,
Dimitrios K. Papadopoulos,
Andrea Leitch,
Olga Murina,
Žygimantė Tarnauskaitė,
Sarah R. Wessel,
Anastasia Zlatanou,
Audrey Vernet,
Alex von Kriegsheim,
Rachel M. A. Mottram
and 47 other authors
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism
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Per Svenningsson,
Rayomand Press,
Ann Nordgren
Expanding the ataxia with oculomotor apraxia type 4 phenotype
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Alicja Winczura,
Andrew N. Blackford,
Valérie Borel,
Edward S. Miller,
Anastasia Zlatanou,
Jadwiga Nieminuszczy,
Ellis L. Ryan,
Nicholas J. Davies,
Tatjana Stankovic,
Simon J. Boulton,
Wojciech Niedzwiedz,
Grant S. Stewart
BOD1L Is Required to Suppress Deleterious Resection of Stressed Replication Forks
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Grant S. Stewart
Reply: A single strand that links multiple neuropathologies in human disease
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Wafaa Eyaid,
Adria Bodell,
Brenda Barry,
Danielle Gleason,
Kathryn Allen,
Vijay S. Ganesh,
Bernard S. Chang,
Arthur Grix,
R. Sean Hill,
R. Sean Hill
and 5 other authors
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
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Sherif F. El Khamisy,
Keith W. Caldecott
Short-patch single-strand break repair in ataxia oculomotor apraxia-1
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