Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1986 1
1990 2
1995 2
1996 3
1997 1
1998 3
2000 2
2001 4
2002 3
2003 3
2004 3
2005 8
2006 10
2007 15
2008 17
2009 10
2010 9
2011 11
2012 10
2013 5
2014 6
2015 3
2016 5
2017 4
2018 3
2019 4
2020 7
2021 14
2022 18
2023 16
2024 16
2025 17

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

209 results

Results by year

Filters applied: . Clear all
Page 1
Epidemiology and causes of preterm birth.
Goldenberg RL, Culhane JF, Iams JD, Romero R. Goldenberg RL, et al. Among authors: culhane jf. Lancet. 2008 Jan 5;371(9606):75-84. doi: 10.1016/S0140-6736(08)60074-4. Lancet. 2008. PMID: 18177778 Free PMC article. Review.
GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia.
Shade LMP, Katsumata Y, Abner EL, Aung KZ, Claas SA, Qiao Q, Heberle BA, Brandon JA, Page ML, Hohman TJ, Mukherjee S, Mayeux RP, Farrer LA, Schellenberg GD, Haines JL, Kukull WA, Nho K, Saykin AJ, Bennett DA, Schneider JA; National Alzheimer’s Coordinating Center; Alzheimer’s Disease Genetics Consortium; Ebbert MTW, Nelson PT, Fardo DW. Shade LMP, et al. Nat Genet. 2024 Nov;56(11):2407-2421. doi: 10.1038/s41588-024-01939-9. Epub 2024 Oct 8. Nat Genet. 2024. PMID: 39379761 Free PMC article.
Stillbirth: a review.
Goldenberg RL, Kirby R, Culhane JF. Goldenberg RL, et al. Among authors: culhane jf. J Matern Fetal Neonatal Med. 2004 Aug;16(2):79-94. doi: 10.1080/14767050400003801. J Matern Fetal Neonatal Med. 2004. PMID: 15512717 Review.
Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults.
Walters S, Contreras AG, Eissman JM, Mukherjee S, Lee ML, Choi SE, Scollard P, Trittschuh EH, Mez JB, Bush WS, Kunkle BW, Naj AC, Peterson A, Gifford KA, Cuccaro ML, Cruchaga C, Pericak-Vance MA, Farrer LA, Wang LS, Haines JL, Jefferson AL, Kukull WA, Keene CD, Saykin AJ, Thompson PM, Martin ER, Bennett DA, Barnes LL, Schneider JA, Crane PK, Hohman TJ, Dumitrescu L; Alzheimer’s Disease Neuroimaging Initiative, Alzheimer’s Disease Genetics Consortium, and Alzheimer’s Disease Sequencing Project. Walters S, et al. JAMA Neurol. 2023 Sep 1;80(9):929-939. doi: 10.1001/jamaneurol.2023.2169. JAMA Neurol. 2023. PMID: 37459083 Free PMC article.
18F-MK-6240 tau PET in patients at-risk for chronic traumatic encephalopathy.
Alosco ML, Mejía Pérez J, Culhane JE, Shankar R, Nowinski CJ, Bureau S, Mundada N, Smith K, Amuiri A, Asken B, Groh JR, Miner A, Pettway E, Mosaheb S, Tripodis Y, Windon C, Mercier G, Stern RA, Grinberg LT, Soleimani-Meigooni DN, Christian BT, Betthauser TJ, Stein TD, McKee AC, Mathis CA, Abrahamson EE, Ikonomovic MD, Johnson SC, Mez J, La Joie R, Schonhaut D, Rabinovici GD. Alosco ML, et al. Among authors: culhane je. Mol Neurodegener. 2025 Feb 25;20(1):23. doi: 10.1186/s13024-025-00808-1. Mol Neurodegener. 2025. PMID: 39994806 Free PMC article.
Racial disparities in preterm birth.
Culhane JF, Goldenberg RL. Culhane JF, et al. Semin Perinatol. 2011 Aug;35(4):234-9. doi: 10.1053/j.semperi.2011.02.020. Semin Perinatol. 2011. PMID: 21798403 Review.
Prevention of preterm birth.
Denney JM, Culhane JF, Goldenberg RL. Denney JM, et al. Among authors: culhane jf. Womens Health (Lond). 2008 Nov;4(6):625-38. doi: 10.2217/17455057.4.6.625. Womens Health (Lond). 2008. PMID: 19072464 Free article. Review.
Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease.
Xicota L, Cosentino S, Vardarajan B, Mayeux R, Perls TT, Andersen SL, Zmuda JM, Thyagarajan B, Yashin A, Wojczynski MK, Krinsky-McHale S, Handen BL, Christian BT, Head E, Mapstone ME, Schupf N, Lee JH, Barral S; Long‐Life Family Study (LLFS); Alzheimer's Disease Genetic Consortium (ADGC); Alzheimer's Biomarkers Consortium‐Down Syndrome (ABC‐DS). Xicota L, et al. Alzheimers Dement. 2024 Apr;20(4):2670-2679. doi: 10.1002/alz.13718. Epub 2024 Feb 21. Alzheimers Dement. 2024. PMID: 38380866 Free PMC article.
Publisher Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia.
Shade LMP, Katsumata Y, Abner EL, Aung KZ, Claas SA, Qiao Q, Heberle BA, Brandon JA, Page ML, Hohman TJ, Mukherjee S, Mayeux RP, Farrer LA, Schellenberg GD, Haines JL, Kukull WA, Nho K, Saykin AJ, Bennett DA, Schneider JA; National Alzheimer’s Coordinating Center; Alzheimer’s Disease Genetics Consortium; Ebbert MTW, Nelson PT, Fardo DW. Shade LMP, et al. Nat Genet. 2025 Jul;57(7):1791. doi: 10.1038/s41588-024-02046-5. Nat Genet. 2025. PMID: 40527985 Free PMC article. No abstract available.
209 results