1. Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015). (July 2016) Authors: Shay, Jerry; Homma, Noriko; Zhou, Ruyun; Naseer, Muhammad; Chaudhary, Adeel; Al-Qahtani, Mohammed; Hirokawa, Nobutaka; Goudarzi, Maryam; Fornace, Albert; Baeesa, Saleh; Hussain, Deema; Bangash, Mohammed; Alghamdi, Fahad; Schulten, Hans-Juergen; Carracedo, Angel; Khan, Ishaq; Qashqari, Hanadi; Mad... Journal: BMC genomics Issue: Volume 17:Number 6(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes. Issue 5 (6th March 2019) Authors: Gallon, Richard; Mühlegger, Barbara; Wenzel, Sören‐Sebastian; Sheth, Harsh; Hayes, Christine; Aretz, Stefan; Dahan, Karin; Foulkes, William; Kratz, Christian P.; Ripperger, Tim; Azizi, Amedeo A.; Baris Feldman, Hagit; Chong, Anne‐Laure; Demirsoy, Ugur; Florkin, Benoît; Imschweiler, Thomas; Janusz... Journal: Human mutation Issue: Volume 40:Issue 5(2019) Page Start: 649 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial. Issue 10240 (13th June 2020) Authors: Burn, John; Sheth, Harsh; Elliott, Faye; Reed, Lynn; Macrae, Finlay; Mecklin, Jukka-Pekka; Möslein, Gabriela; McRonald, Fiona E; Bertario, Lucio; Evans, D Gareth; Gerdes, Anne-Marie; Ho, Judy W C; Lindblom, Annika; Morrison, Patrick J; Rashbass, Jem; Ramesar, Raj; Seppälä, Toni; Thomas, Huw J W; ... Journal: Lancet Issue: Volume 395:Issue 10240(2020) Page Start: 1855 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. PTU-050 The successful implementation of fast-track routine testing for microsatellite instability in a colorectal cancer pathway. (8th June 2018) Authors: Ngu, Wee Sing; Mills, Sarah; Sheth, Harsh; Burn, John; Lee, Thomas Journal: Gut Issue: Volume 67(2018)Supplement 1 Page Start: A196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Infarcted accessory spleen masquerading as a mesenteric cyst. (16th August 2018) Authors: Sheth, Harsh; Chaudhari, Sadashiv; Sinha, Yash; Prajapati, Ramlal Journal: BMJ case reports Issue: Volume 2018 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. O35 Screening for lynch syndrome in cases of colorectal cancer: identifying barriers in a fast-track pathway. (19th June 2022) Authors: Lee, Tom; Glover, Eleanor; Ngu, Lena; Gibson, Philip; Sheth, Harsh; Gallon, Richard; Martin, Richard; Jackson, Michael; Mills, Sarah; Burn, John Journal: Gut Issue: Volume 71(2022)Supplement 1 Page Start: A21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Sequencing‐based microsatellite instability testing using as few as six markers for high‐throughput clinical diagnostics. Issue 1 (15th September 2019) Authors: Gallon, Richard; Sheth, Harsh; Hayes, Christine; Redford, Lisa; Alhilal, Ghanim; O'Brien, Ottilia; Spiewak, Helena; Waltham, Amanda; McAnulty, Ciaron; Izuogu, Osagie G.; Arends, Mark J.; Oniscu, Anca; Alonso, Angel M.; Laguna, Sira M.; Borthwick, Gillian M.; Santibanez‐Koref, Mauro; Jackson, Mich... Journal: Human mutation Issue: Volume 41:Issue 1(2020) Page Start: 332 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Screening by single-molecule molecular inversion probes targeted sequencing panel of candidate genes of infertility in azoospermic infertile Jordanian males. (20th October 2022) Authors: Batiha, Osamah; Burghel, George J.; Alkofahi, Ayesha; Alsharu, Emad; Smith, Hannah; Alobaidi, Bilal; Al-Smadi, Mohammad; Awamlah, Nour; Hussein, Lama; Abdelnour, Amid; Sheth, Harsh; Veltman, Joris Journal: Human fertility Issue: Volume 25:Number 5(2022) Page Start: 939 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database. (April 2023) Authors: Dominguez-Valentin, Mev; Haupt, Saskia; Seppälä, Toni T.; Sampson, Julian R.; Sunde, Lone; Bernstein, Inge; Jenkins, Mark A.; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capella, Gabriel; Balaguer, Francesc; Evans, Dafydd Gareth; Burn, John; Holinski-Feder, Elke; Bertario, Lucio; Bonanni, ... Journal: EClinicalMedicine Issue: Volume 58(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗