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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1997 2
1998 4
1999 3
2000 1
2001 1
2002 5
2003 1
2004 4
2007 3
2008 1
2010 5
2011 3
2012 3
2013 8
2014 4
2015 7
2016 4
2017 3
2018 2
2019 3
2020 7
2021 5
2022 8
2023 6
2024 0

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86 results

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Page 1
Genome sequencing reveals underdiagnosis of primary ciliary dyskinesia in bronchiectasis.
Shoemark A, Griffin H, Wheway G, Hogg C, Lucas JS; Genomics England Research Consortium; Camps C, Taylor J, Carroll M, Loebinger MR, Chalmers JD, Morris-Rosendahl D, Mitchison HM, De Soyza A; Genomics England Research Consortium:; Brown D, Ambrose JC, Arumugam P, Bevers R, Bleda M, Boardman-Pretty F, Boustred CR, Brittain H, Caulfield MJ, Chan GC, Fowler T, Giess A, Hamblin A, Henderson S, Hubbard TJP, Jackson R, Jones LJ, Kasperaviciute D, Kayikci M, Kousathanas A, Lahnstein L, Leigh SEA, Leong IUS, Lopez FJ, Maleady-Crowe F, McEntagart M, Minneci F, Moutsianas L, Mueller M, Murugaesu N, Need AC, O'Donovan P, Odhams CA, Patch C, Perez-Gil D, Pereira MB, Pullinger J, Rahim T, Rendon A, Rogers T, Savage K, Sawant K, Scott RH, Siddiq A, Sieghart A, Smith SC, Sosinsky A, Stuckey A, Tanguy M, Taylor Tavares AL, Thomas ERA, Thompson SR, Tucci A, Welland MJ, Williams E, Witkowska K, Wood SM. Shoemark A, et al. Among authors: morris rosendahl d. Eur Respir J. 2022 Nov 17;60(5):2200176. doi: 10.1183/13993003.00176-2022. Print 2022 Nov. Eur Respir J. 2022. PMID: 35728977
COPD in the chromosomes.
Cockbain B, Morris-Rosendahl D, Corrigan A, Hind MD. Cockbain B, et al. Among authors: morris rosendahl d. Thorax. 2022 May 12:thoraxjnl-2022-218782. doi: 10.1136/thoraxjnl-2022-218782. Online ahead of print. Thorax. 2022. PMID: 35552249 No abstract available.
Autosomal Recessive Primary Microcephaly (MCPH): An Update.
Zaqout S, Morris-Rosendahl D, Kaindl AM. Zaqout S, et al. Among authors: morris rosendahl d. Neuropediatrics. 2017 Jun;48(3):135-142. doi: 10.1055/s-0037-1601448. Epub 2017 Apr 11. Neuropediatrics. 2017. PMID: 28399591 Review.
The role of genetics and genomics in clinical psychiatry.
Hoehe MR, Morris-Rosendahl DJ. Hoehe MR, et al. Among authors: morris rosendahl dj. Dialogues Clin Neurosci. 2018 Sep;20(3):169-177. doi: 10.31887/DCNS.2018.20.3/mhoehe. Dialogues Clin Neurosci. 2018. PMID: 30581286 Free PMC article. Review.
The genetic basis of thoracic aortic disease: The future of aneurysm classification?
Salmasi MY, Alwis S, Cyclewala S, Jarral OA, Mohamed H, Mozalbat D, Nienaber CA, Athanasiou T, Morris-Rosendahl D; Members of the London Aortic Mechanobiology Working Group. Salmasi MY, et al. Among authors: morris rosendahl d. Hellenic J Cardiol. 2023 Jan-Feb;69:41-50. doi: 10.1016/j.hjc.2022.09.009. Epub 2022 Oct 3. Hellenic J Cardiol. 2023. PMID: 36202327 Free article. Review.
BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients.
Engel C, Valence S, Delplancq G, Maroofian R, Accogli A, Agolini E, Alkuraya FS, Baglioni V, Bagnasco I, Becmeur-Lefebvre M, Bertini E, Borggraefe I, Brischoux-Boucher E, Bruel AL, Brusco A, Bubshait DK, Cabrol C, Cilio MR, Cornet MC, Coubes C, Danhaive O, Delague V, Denommé-Pichon AS, Di Giacomo MC, Doco-Fenzy M, Engels H, Cremer K, Gérard M, Gleeson JG, Heron D, Goffeney J, Guimier A, Harms FL, Houlden H, Iacomino M, Kaiyrzhanov R, Kamien B, Karimiani EG, Kraus D, Kuentz P, Kutsche K, Lederer D, Massingham L, Mignot C, Morris-Rosendahl D, Nagarajan L, Odent S, Ormières C, Partlow JN, Pasquier L, Penney L, Philippe C, Piccolo G, Poulton C, Putoux A, Rio M, Rougeot C, Salpietro V, Scheffer I, Schneider A, Srivastava S, Straussberg R, Striano P, Valente EM, Venot P, Villard L, Vitobello A, Wagner J, Wagner M, Zaki MS, Zara F, Lesca G, Yassaee VR, Miryounesi M, Hashemi-Gorji F, Beiraghi M, Ashrafzadeh F, Galehdari H, Walsh C, Novelli A, Tacke M, Sadykova D, Maidyrov Y, Koneev K, Shashkin C, Capra V, Zamani M, Van Maldergem L, Burglen L, Piard J. Engel C, et al. Among authors: morris rosendahl d. Eur J Hum Genet. 2023 Sep;31(9):1023-1031. doi: 10.1038/s41431-023-01410-z. Epub 2023 Jun 21. Eur J Hum Genet. 2023. PMID: 37344571
EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias.
Hayesmoore JB, Bhuiyan ZA, Coviello DA, du Sart D, Edwards M, Iascone M, Morris-Rosendahl DJ, Sheils K, van Slegtenhorst M, Thomson KL. Hayesmoore JB, et al. Among authors: morris rosendahl dj. Eur J Hum Genet. 2023 Sep;31(9):1003-1009. doi: 10.1038/s41431-023-01421-w. Epub 2023 Jul 13. Eur J Hum Genet. 2023. PMID: 37443332 Free PMC article. Review.
Warburg Micro syndrome.
Dursun F, Güven A, Morris-Rosendahl D. Dursun F, et al. Among authors: morris rosendahl d. J Pediatr Endocrinol Metab. 2012;25(3-4):379-82. doi: 10.1515/jpem-2011-0459. J Pediatr Endocrinol Metab. 2012. PMID: 22768674
86 results