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D

David Parry

The University of Edinburgh

101H-index
632Paper Count
3.4WCitation Count
Published Papers 132
Publication Date
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A progeria syndrome links DNA hypermethylation to age-related pathology
errNature Genetics
IF29
err2026-06-12
err0
errOAAI
errDan Sarni; Gráinne Neary; Paula L. Carroll; Chris S. Vink; Caroline V. Billard; Tomoya Isobe; Xiong Weng; Jordan R. Portman; Daniel L. McCartney; Patricia Heyn; Rob J. van ‘t Hof; Linda R. Morrison; Carol-Anne Martin; Colin Stok; Margaret E. Harley; Andrea Leitch; Maarten van den Ancker; Nic Robertson; Laura Kitto; Richard Clark; Michael Rennie; Anna Popravko; Jessica J. McClure; David A. Parry; Giuseppina Camiolo; Tom Leah; Hélène Jakobczyk; Roly Megaw; Lisa McKie; Grant F. Marshall; Nika Balkic; Jeanne Amiel; Tania Barragán Arévalo; Grace Bronken McCarthy; Catherine A. Buchanan; Alexandre Buffet; Alberto Cascón; Benjamin Cogne; Solene Conrad; Anna Maria Cueto-González; Maria Currás-Freixes; Gunnar Douzgos Houge; Chin-To Fong; Jaya K. George-Abraham; Kate Gibson; Lourdes Ibáñez; Nicola Longo; Charlotte Lussey-Lepoutre; Bradley S. Miller; Alejandro Moles-Fernandez; Nishitha R. Pillai; Tatiana Tvrdik; Marie Vincent; Emiy Yokoyama; Catherine M. Abbott; Francisco Jose Sanchez-Luque; Katrin Ottersbach; Cosimo De Bari; Anke J. Roelofs; Rebekah Tillotson; Kamil R. Kranc; Sara J. Brown; Riccardo E. Marioni; Mihaela Crisan; Berthold Göttgens; Neil C. Henderson; Robert K. Semple; Kevin B. Myant; Elaine Dzierzak; Martin A. M. Reijns; Duncan Sproul; Andrew P. Jackson
errShare
errSave
Lymphoid B cells upregulate HIV-1 ex vivo and are linked to its expression in vivo
errPLOS PATHOGENS
IF4.9
err2025-12-01
err0
PREAI
errOllerton, Matthew T.; Folkvord, Joy M.; Bush, Veronica; Parry, David A.; Meditz, Amie L.; Mccarter, Martin D.; Yost, Fred; Shikuma, Cecilia M.; Connick, Elizabeth
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errSave
Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures
erramerican journal of human genetics
IF0
err2025-06-18
err0
PREAI
errSankalita Ray Das; Rosie Sullivan; Mischa S.G. Ruegg; Julia Horsfield; Jordan Doran; Gemma Poke; Nathalie de Vries; Sarah Duerinckx; Damien Lederer; Muzhirah Haniffa; Wee-Teik Keng; Gaik-Siew Ch’ng; David A. Parry; Andrew P. Jackson; Masamune Sakamoto; Naomichi Matsumoto; Noriko Miyake; Shin Nabatame; Hidetoshi Taniguchi; Emma Wakeling; Katrin Õunap; Pilvi Ilves; Ghayda Mirzaa; Andrew Timms; Emily Pao; Kimberly A. Aldinger; William Dobyns; Axel Bohring; Beate Behre; Daniel G. Calame; James R. Lupski; Juan M. Pascual; Marc Abramowicz; Gregory Gimenez; Louise S. Bicknell
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errSave
CDK4 loss-of-function mutations cause microcephaly and short stature
errGENES & DEVELOPMENT
IF7.7
err2025-04-10
err0
errOAAI
errVerdu Schlie, Aitana; Leitch, Andrea; Arismendi, Maria Izabel; Stok, Colin; Castro Leal, Andrea; Parry, David A.; Lerario, Antonio Marcondes; Harley, Margaret E.; Lucheze, Bruna; Carroll, Paula L.; Musialik, Kamila I.; Auer, Julia M. T.; Martin, Carol-Anne; Gerasimavicius, Lukas; Quigley, Alan J.; Correia-Deur, Joya Emilie de Menezes; Marsh, Joseph A.; Reijns, Martin A. M.; Lampe, Anne K.; Jackson, Andrew P.; Jorge, Alexander A. L.; Tamayo-Orrego, Lukas
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errSave
Whole Genome Sequencing of Mutation-Negative Individuals With Cornelia de Lange Syndrome
errHUMAN MUTATION
IF3.7
err2025-01-30
err0
errOAAI
errAnsari, Morad; Halachev, Mihail; Parry, David; Campos, Jose L.; D'Souza, Elston N.; Barnett, Christopher; Wilkie, Andrew O. M.; Barnicoat, Angela; Patel, Chirag V.; Sukarova-Angelovska, Elena; Girisha, Katta M.; Firth, Helen V.; Prescott, Katrina; Wilson, Louise C.; Mcentagart, Meriel; Davidson, Rosemarie; Lynch, Sally Ann; Joss, Shelagh; Holden, Simon T.; Lam, Wayne K.; Sisodiya, Sanjay M.; Green, Andrew J.; Poke, Gemma; Whiffin, Nicola; Fitzpatrick, David R.; Meynert, Alison
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errSave
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder ( vol 103 , pg 221 , 2018)
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2024-05-01
err1
errOAAI
errMartin, Carol-Anne; Sarlos, Kata; Logan, Clare, V; Thakur, Roshan Singh; Parry, David A.; Bizard, Anna H.; Leitch, Andrea; Cleal, Louise; Ali, Nadia Shaukat; Al-Owain, Mohammed A.; Allen, William; Altmueller, Janine; Aza-Carmona, Miriam; Barakat, Bushra A. Y.; Barraza-Garcia, Jimena; Begtrup, Amber; Bogliolo, Massimo; Cho, Megan T.; Cruz-Rojo, Jaime; Dhahrabi, Hassan Ali Mundi; Elcioglu, Nursel H.; Gorman, Grainne S.; Jobling, Rebekah; Kesterton, Ian; Kishita, Yoshihito; Kohda, Masakazu; Stabej, Polona Le Quesne; Malallah, Asam Jassim; Nurnberg, Peter; Ohtake, Akira; Okazaki, Yasushi; Pujol, Roser; Ramirez, Maria Jose; Revah-Politi, Anya; Shimura, Masaru; Stevens, Paul; Taylor, Robert W.; Turner, Lesley; Williams, Hywel; Wilson, Carolyn; Yigit, Goekhan; Zahavich, Laura; Alkuraya, Fowzan S.; Surralles, Jordi; Iglesias, Alejandro; Murayama, Kei; Wollnik, Bernd; Dattani, Mehul; Heath, Karen E.; Hickson, Ian D.; Jackson, Andrew P.
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errSave
Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2023-11-30
err3
errOAAI
errHall, Hildegard Nikki; Parry, David; Halachev, Mihail; Williamson, Kathleen A.; Donnelly, Kevin; Campos Parada, Jose; Bhatia, Shipra; Joseph, Jeffrey; Holden, Simon; Prescott, Trine E.; Bitoun, Pierre; Kirk, Edwin P.; Newbury-Ecob, Ruth; Lachlan, Katherine; Bernar, Juan; van Heyningen, Veronica; Fitzpatrick, David R.; Meynert, Alison
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errSave
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2023-10-09
err4
errOAAI
errVandersteen, Anthony M.; Weerakkody, Ruwan A.; Parry, David A.; Kanonidou, Christina; Toddie-Moore, Daniel J.; Vandrovcova, Jana; Darlay, Rebecca; Santoyo-Lopez, Javier; Meynert, Alison; Kazkaz, Hanadi; Grahame, Rodney; Cummings, Carole; Bartlett, Marion; Ghali, Neeti; Brady, Angela F.; Pope, F. Michael; van Dijk, Fleur S.; Cordell, Heather J.; Aitman, Timothy J.
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errSave
Raf-induced proliferation or cell cycle arrest is determined by the level of Raf activity with arrest mediated by p21(Cip1)
errMOLECULAR AND CELLULAR BIOLOGY
IF2.7
err2023-03-29
err639
errOAAI
errWoods, D; Parry, D; Cherwinski, H; Bosch, E; Lees, E; McMahon, M
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errSave
Intra-S-phase checkpoint activation by direct CDK2 inhibition
errMOLECULAR AND CELLULAR BIOLOGY
IF2.7
err2023-03-27
err69
errOAAI
errZhu, YH; Alvarez, C; Doll, R; Kurata, H; Schebye, XM; Parry, D; Lees, E
errShare
errSave
Regulatory de novo mutations underlying intellectual disability
errLIFE SCIENCE ALLIANCE
IF2.9
err2023-02-28
err2
errOAAI
errVas, Matias G. De; Boulet, Fanny; Joshi, Shweta S.; Garstang, Myles G.; Khan, Tahir N.; Atla, Goutham; Parry, David; Moore, David; Cebola, Ines; Zhang, Shuchen; Cui, Wei; Lampe, Anne K.; Lam, Wayne W.; Ferrer, Jorge; Pradeepa, Madapura M.; Atanur, Santosh S.
errShare
errSave
Follicular regulatory T cells eliminate HIV-1-infected follicular helper T cells in an IL-2 concentration dependent manner
errFRONTIERS IN IMMUNOLOGY
IF5.9
err2022-11-07
err0
errOAAI
errOllerton, Matthew T. T.; Folkvord, Joy M. M.; La Mantia, Andriana; Parry, David A. A.; Meditz, Amie L. L.; McCarter, Martin D. D.; D'Aquila, Richard T.; Connick, Elizabeth
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errSave
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy
errNATURE COMMUNICATIONS
IF15.7
err2022-11-04
err20
errOAAI
errGrange, Laura J.; Reynolds, John J.; Ullah, Farid; Isidor, Bertrand; Shearer, Robert F.; Latypova, Xenia; Baxley, Ryan M.; Oliver, Antony W.; Ganesh, Anil; Cooke, Sophie L.; Jhujh, Satpal S.; McNee, Gavin S.; Hollingworth, Robert; Higgs, Martin R.; Natsume, Toyoaki; Khan, Tahir; Martos-Moreno, Gabriel A.; Chupp, Sharon; Mathew, Christopher G.; Parry, David; Simpson, Michael A.; Nahavandi, Nahid; Yuksel, Zafer; Drasdo, Mojgan; Kron, Anja; Vogt, Petra; Jonasson, Annemarie; Seth, Saad Ahmed; Gonzaga-Jauregui, Claudia; Brigatti, Karlla W.; Stegmann, Alexander P. A.; Kanemaki, Masato; Josifova, Dragana; Uchiyama, Yuri; Oh, Yukiko; Morimoto, Akira; Osaka, Hitoshi; Ammous, Zineb; Argente, Jesus; Matsumoto, Naomichi; Stumpel, Constance T. R. M.; Taylor, Alexander M. R.; Jackson, Andrew P.; Bielinsky, Anja-Katrin; Mailand, Niels; Le Caignec, Cedric; Davis, Erica E.; Stewart, Grant S.
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errSave
240 Flexor Digitorum Profundus Tendon Segment Length Estimation via Measurement of Adjacent Landmarks in the Secondary Repair of Jersey Finger
errBRITISH JOURNAL OF SURGERY
IF8.7
err2022-08-19
err0
errOAAI
errSehmbi, A.; Syed, M.; Shah, S.; Parry, D.
errShare
errSave
Loss of Integrin-Linked Kinase Sensitizes Breast Cancer to SRC Inhibitors
errCANCER RESEARCH
IF16.6
err2021-12-17
err7
errOAAI
errBeetham, Henry; Griffith, Billie G. C.; Murina, Olga; Loftus, Alexander E. P.; Parry, David A.; Temps, Carolin; Culley, Jayne; Muir, Morwenna; Unciti-Broceta, Asier; Sims, Andrew H.; Byron, Adam; Brunton, Valerie G.
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errSave
Keratin intermediate filament chains in the European common wall lizard (Podarcis muralis) and a potential keratin filament crosslinker
errJOURNAL OF STRUCTURAL BIOLOGY
IF5.1
err2021-12-01
err4
PREAI
errParry, David A. D.; Winter, David J.
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errSave
Intragenic copy number variation in mouse epiplakin 1 (Eppk1) and the conservation of the repeat structures in the lower vertebrates
errJOURNAL OF DERMATOLOGICAL SCIENCE
IF4
err2021-09-01
err4
PREAI
errUeo, Daisuke; Furuhashi, Mie; Sasaki, Takashi; Kudoh, Jun; Parry, David A. D.; Winter, David J.; Sasaki, Takako; Hashimoto, Takashi; Tsuruta, Daisuke; Fujiwara, Sakuhei
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errSave
Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2021-05-20
err12
errOAAI
errDuker, Angela L.; Kinderman, Dagmar; Jordan, Christy; Niiler, Tim; Baker-Smith, Carissa M.; Thompson, Louise; Parry, David A.; Carroll, Ricki S.; Bober, Michael B.
errShare
errSave
Keratin intermediate filament chains in tuatara (Sphenodon punctatus): A comparison of tuatara and human sequences
errJOURNAL OF STRUCTURAL BIOLOGY
IF5.1
err2021-03-01
err6
PREAI
errParry, David A. D.; Winter, David J.
errShare
errSave
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy
errGENETICS IN MEDICINE
IF6.2
err2021-02-01
err38
errOAAI
errParry, David A.; Martin, Carol-Anne; Greene, Philip; Marsh, Joseph A.; Blyth, Moira; Cox, Helen; Donnelly, Deirdre; Greenhalgh, Lynn; Greville-Heygate, Stephanie; Harrison, Victoria; Lachlan, Katherine; McKenna, Caoimhe; Quigley, Alan J.; Rea, Gillian; Robertson, Lisa; Suri, Mohnish; Jackson, Andrew P.
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Research Directions

No research directions
Co-authors
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