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

Year Number of Results
1948 1
1981 4
1982 9
1983 5
1984 3
1986 4
1987 3
1988 5
1989 4
1990 7
1991 3
1992 7
1993 4
1994 7
1995 12
1996 7
1997 13
1998 8
1999 9
2000 6
2001 4
2002 10
2003 1
2004 7
2005 2
2006 3
2007 6
2008 6
2009 5
2010 4
2011 1
2012 5
2013 8
2014 8
2015 6
2016 8
2017 6
2018 10
2019 14
2020 14
2021 13
2022 8
2023 12
2024 7

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272 results

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Page 1
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
Dougherty GW, Mizuno K, Nöthe-Menchen T, Ikawa Y, Boldt K, Ta-Shma A, Aprea I, Minegishi K, Pang YP, Pennekamp P, Loges NT, Raidt J, Hjeij R, Wallmeier J, Mussaffi H, Perles Z, Elpeleg O, Rabert F, Shiratori H, Letteboer SJ, Horn N, Young S, Strünker T, Stumme F, Werner C, Olbrich H, Takaoka K, Ide T, Twan WK, Biebach L, Große-Onnebrink J, Klinkenbusch JA, Praveen K, Bracht DC, Höben IM, Junger K, Gützlaff J, Cindrić S, Aviram M, Kaiser T, Memari Y, Dzeja PP, Dworniczak B, Ueffing M, Roepman R, Bartscherer K, Katsanis N, Davis EE, Amirav I, Hamada H, Omran H. Dougherty GW, et al. Nat Commun. 2020 Nov 2;11(1):5520. doi: 10.1038/s41467-020-19113-0. Nat Commun. 2020. PMID: 33139725 Free PMC article.
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.
Dougherty GW, Ostrowski LE, Nöthe-Menchen T, Raidt J, Schramm A, Olbrich H, Yin W, Sears PR, Dang H, Smith AJ, Beule AG, Hjeij R, Rutjes N, Haarman EG, Maas SM, Ferkol TW, Noone PG, Olivier KN, Bracht DC, Barbry P, Zaragosi LE, Fierville M, Kliesch S, Wohlgemuth K, König J, George S, Loges NT, Ceppe A, Markovetz MR, Luo H, Guo T, Rizk H, Eldesoky T, Dahlke K, Boldt K, Ueffing M, Hill DB, Pang YP, Knowles MR, Zariwala MA, Omran H. Dougherty GW, et al. Am J Respir Crit Care Med. 2024 Jul 1;210(1):63-76. doi: 10.1164/rccm.202308-1370OC. Am J Respir Crit Care Med. 2024. PMID: 38626355 Free PMC article.
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly.
Wallmeier J, Bracht D, Alsaif HS, Dougherty GW, Olbrich H, Cindric S, Dzietko M, Heyer C, Teig N, Thiels C, Faqeih E, Al-Hashim A, Khan S, Mogarri I, Almannai M, Al Otaibi W, Alkuraya FS, Koerner-Rettberg C, Omran H. Wallmeier J, et al. Among authors: dougherty gw. Am J Hum Genet. 2021 Jul 1;108(7):1318-1329. doi: 10.1016/j.ajhg.2021.05.002. Epub 2021 Jun 1. Am J Hum Genet. 2021. PMID: 34077761 Free PMC article.
A sense of danger from radiation.
McBride WH, Chiang CS, Olson JL, Wang CC, Hong JH, Pajonk F, Dougherty GJ, Iwamoto KS, Pervan M, Liao YP. McBride WH, et al. Among authors: dougherty gj. Radiat Res. 2004 Jul;162(1):1-19. doi: 10.1667/rr3196. Radiat Res. 2004. PMID: 15222781 Review.
Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility.
Aprea I, Wilken A, Krallmann C, Nöthe-Menchen T, Olbrich H, Loges NT, Dougherty GW, Bracht D, Brenker C, Kliesch S, Strünker T, Tüttelmann F, Raidt J, Omran H. Aprea I, et al. Among authors: dougherty gw. Front Genet. 2023 Feb 17;14:1117821. doi: 10.3389/fgene.2023.1117821. eCollection 2023. Front Genet. 2023. PMID: 36873931 Free PMC article.
Radiotherapy for genes that cause cancer.
McBride WH, Dougherty GJ. McBride WH, et al. Among authors: dougherty gj. Nat Med. 1995 Nov;1(11):1215-7. doi: 10.1038/nm1195-1215. Nat Med. 1995. PMID: 7584999 Review.
Modernizing Journal Club to Teach Evidence-Based Practice.
Qulisy E, Dougherty G, Hothan K, Dandavino M. Qulisy E, et al. Among authors: dougherty g. Med Educ. 2023 Aug;57(8):772-773. doi: 10.1111/medu.15113. Epub 2023 May 14. Med Educ. 2023. PMID: 37183290 No abstract available.
CD44 isoforms in normal and leukemic hematopoiesis.
Ghaffari S, Smadja-Joffe F, Oostendorp R, Lévesque JP, Dougherty G, Eaves A, Eaves C. Ghaffari S, et al. Among authors: dougherty g. Exp Hematol. 1999 Jun;27(6):978-93. doi: 10.1016/s0301-472x(99)00023-5. Exp Hematol. 1999. PMID: 10378887 Free article. Review. No abstract available.
Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia.
Hjeij R, Aprea I, Poeta M, Nöthe-Menchen T, Bracht D, Raidt J, Honecker BI, Dougherty GW, Olbrich H, Schwartz O, Keller U, Nüsse H, Diderich KEM, Vogelberg C, Santamaria F, Omran H. Hjeij R, et al. Among authors: dougherty gw. Genet Med. 2023 May;25(5):100798. doi: 10.1016/j.gim.2023.100798. Epub 2023 Jan 31. Genet Med. 2023. PMID: 36727596 Free article.
272 results