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Author/Creator Rahbari, Raheleh

2. Inherent Mosaicism and Extensive Mutation of Human Placentas. Issue 6 (June 2021)

Authors:
Coorens, Tim H. H.; Oliver, Thomas R. W.; Sanghvi, Rashesh; Sovio, Ulla; Cook, Emma; Vento-Tormo, Roser; Haniffa, Muzlifah; Young, Matthew D.; Rahbari, Raheleh; Sebire, Neil; Campbell, Peter J.; Charnock-Jones, D. Stephen; Smith, Gordon C. S.; Behjati, Sam
Journal:
Obstetrical & gynecological survey
Issue:
Volume 76:Issue 6(2021)
Page Start:
Record Type:
Journal Article
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3. Meiosis and beyond – understanding the mechanistic and evolutionary processes shaping the germline genome. (1st January 2021)

Authors:
Bergero, Roberta; Ellis, Peter; Haerty, Wilfried; Larcombe, Lee; Macaulay, Iain; Mehta, Tarang; Mogensen, Mette; Murray, David; Nash, Will; Neale, Matthew J.; O'Connor, Rebecca; Ottolini, Christian; Peel, Ned; Ramsey, Luke; Skinner, Ben; Suh, Alexander; Summers, Michael; Sun, Yu; Tidy, Alison; Ra...
Journal:
Biological reviews
Issue:
Volume 96:Number 3(2021)
Page Start:
822
Record Type:
Journal Article
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4. Small non‐coding RNA sequencing reveals global dysregulation of piwi‐interacting RNA (piRNA) expression in gonadal malignant germ cell tumours. (26th October 2022)

Authors:
Laidlaw, Sean; Alonso‐Crisostomo, Luz; Bailey, Shivani; Saini, Harpreet K.; Molnár, Attila; Nicholson, James C.; Enright, Anton J.; Scarpini, Cinzia G.; Rahbari, Raheleh; Coleman, Nicholas; Murray, Matthew J.
Journal:
Andrology
Issue:
Volume 11:Number 4(2023)
Page Start:
738
Record Type:
Journal Article
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6. Understanding the Genomic Structure of Copy‐Number Variation of the Low‐Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid Arthritis. Issue 4 (15th February 2017)

Authors:
Rahbari, Raheleh; Zuccherato, Luciana W; Tischler, German; Chihota, Belinda; Ozturk, Hasret; Saleem, Sara; Tarazona‐Santos, Eduardo; Machado, Lee R; Hollox, Edward J
Journal:
Human mutation
Issue:
Volume 38:Issue 4(2017)
Page Start:
390
Record Type:
Journal Article
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