| 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 … J Burn, H Sheth, F Elliott, L Reed, F Macrae, JP Mecklin, G Möslein, ... The Lancet 395 (10240), 1855-1863, 2020 | 310 | 2020 |
| Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study FJ Sheth, T Liehr, P Kumari, R Akinde, HJ Sheth, JJ Sheth Indian journal of human genetics 19 (4), 415, 2013 | 82 | 2013 |
| A de novo paradigm for male infertility MS Oud, RM Smits, HE Smith, FK Mastrorosa, GS Holt, BJ Houston, ... Nature communications 13 (1), 154, 2022 | 53 | 2022 |
| Identification of a neuronal transcription factor network involved in medulloblastoma development M Łastowska, H Al-Afghani, HH Al-Balool, H Sheth, E Mercer, ... Acta neuropathologica communications 1, 1-16, 2013 | 51 | 2013 |
| A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes R Gallon, B Mühlegger, SS Wenzel, H Sheth, C Hayes, S Aretz, K Dahan, ... Human mutation 40 (5), 649-655, 2019 | 43 | 2019 |
| Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders MS Oud, BJ Houston, L Volozonoka, FK Mastrorosa, GS Holt, ... Human Reproduction 36 (9), 2597-2611, 2021 | 40 | 2021 |
| The role of aspirin in preventing colorectal cancer J Burn, H Sheth British Medical Bulletin 119 (1), 17-24, 2016 | 37 | 2016 |
| Cancer prevention with resistant starch in Lynch syndrome patients in the CAPP2-randomized placebo controlled trial: planned 10-year follow-up JC Mathers, F Elliott, F Macrae, JP Mecklin, G Möslein, FE McRonald, ... Cancer prevention research 15 (9), 623-634, 2022 | 35 | 2022 |
| Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium P Møller, T Seppälä, JG Dowty, S Haupt, M Dominguez-Valentin, L Sunde, ... Hereditary cancer in clinical practice 20 (1), 36, 2022 | 30 | 2022 |
| Characterization of sSMC by FISH and molecular techniques F Sheth, J Andrieux, E Ewers, N Kosyakova, A Weise, H Sheth, ... European Journal of Medical Genetics 54 (3), 247-255, 2011 | 30 | 2011 |
| 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 … M Dominguez-Valentin, S Haupt, TT Seppälä, JR Sampson, L Sunde, ... EClinicalMedicine 58, 2023 | 27 | 2023 |
| A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and … L Redford, G Alhilal, S Needham, O O’Brien, J Coaker, J Tyson, ... PLoS One 13 (8), e0203052, 2018 | 24 | 2018 |
| Sequencing‐based microsatellite instability testing using as few as six markers for high‐throughput clinical diagnostics R Gallon, H Sheth, C Hayes, L Redford, G Alhilal, O O'Brien, H Spiewak, ... Human Mutation 41 (1), 332-341, 2020 | 22 | 2020 |
| Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) Jeddah, Kingdom of Saudi Arabia. 30 November-3 December 2015 JW Shay, N Homma, R Zhou, MI Naseer, AG Chaudhary, M Al-Qahtani, ... BMC genomics 17, 1-78, 2016 | 13 | 2016 |
| Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations H Sheth, E Northwood, CM Ulrich, D Scherer, F Elliott, JH Barrett, ... PLoS One 13 (2), e0192223, 2018 | 12 | 2018 |
| Association of stroke and bleed events in non-valvular atrial fibrillation patients with direct oral anticoagulant prescriptions in NHS England between 2013 and 2016 H Sheth, D McNally, M Santibanez-Koref, J Burn Plos one 14 (6), e0218878, 2019 | 8 | 2019 |
| Triple-X syndrome in a trisomic Down syndrome child: both aneuploidies originated from the mother HJ Sheth, A Munoz, C Sergi, J Pani, JL Blouin, JJ Sheth, FJ Sheth International Journal of Human Genetics 11 (1), 51-53, 2011 | 6 | 2011 |
| Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test F Sheth, J Shah, D Jain, S Shah, H Patel, K Patel, DI Solanki, AS Iyer, ... BMC neurology 23 (1), 292, 2023 | 5 | 2023 |
| Narrative review on genetic counseling for hereditary cancers: General considerations E Ulhaq, F Huda, C Suhail, H Sheth, RI Anu Cancer Research, Statistics, and Treatment 6 (2), 239-247, 2023 | 5 | 2023 |
| An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene … S Bajaj, P Satoskar, A Nair, F Sheth, J Sheth, H Sheth BMC pediatrics 22 (1), 78, 2022 | 5 | 2022 |
