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Page 1
Extreme drought impacts have been underestimated in grasslands and shrublands globally.
Smith MD, Wilkins KD, Holdrege MC, Wilfahrt P, Collins SL, Knapp AK, Sala OE, Dukes JS, Phillips RP, Yahdjian L, Gherardi LA, Ohlert T, Beier C, Fraser LH, Jentsch A, Loik ME, Maestre FT, Power SA, Yu Q, Felton AJ, Munson SM, Luo Y, Abdoli H, Abedi M, Alados CL, Alberti J, Alon M, An H, Anacker B, Anderson M, Auge H, Bachle S, Bahalkeh K, Bahn M, Batbaatar A, Bauerle T, Beard KH, Behn K, Beil I, Biancari L, Blindow I, Bondaruk VF, Borer ET, Bork EW, Bruschetti CM, Byrne KM, Cahill JF Jr, Calvo DA, Carbognani M, Cardoni A, Carlyle CN, Castillo-Garcia M, Chang SX, Chieppa J, Cianciaruso MV, Cohen O, Cordeiro AL, Cusack DF, Dahlke S, Daleo P, D'Antonio CM, Dietterich LH, S Doherty T, Dubbert M, Ebeling A, Eisenhauer N, Fischer FM, Forte TGW, Gebauer T, Gozalo B, Greenville AC, Guidoni-Martins KG, Hannusch HJ, Vatsø Haugum S, Hautier Y, Hefting M, Henry HAL, Hoss D, Ingrisch J, Iribarne O, Isbell F, Johnson Y, Jordan S, Kelly EF, Kimmel K, Kreyling J, Kröel-Dulay G, Kröpfl A, Kübert A, Kulmatiski A, Lamb EG, Larsen KS, Larson J, Lawson J, Leder CV, Linstädter A, Liu J, Liu S, Lodge AG, Longo G, Loydi A, Luan J, Curtis Lubbe F, Macfarlane C, Mackie-Haas K, Malyshev AV, Maturano-Ruiz A,… See abstract for full author list ➔ Smith MD, et al. Among authors: tedder m. Proc Natl Acad Sci U S A. 2024 Jan 23;121(4):e2309881120. doi: 10.1073/pnas.2309881120. Epub 2024 Jan 8. Proc Natl Acad Sci U S A. 2024. PMID: 38190514 Free PMC article.
The detection of a strong episignature for Chung-Jansen syndrome, partially overlapping with Börjeson-Forssman-Lehmann and White-Kernohan syndromes.
Vos N, Haghshenas S, van der Laan L, Russel PKM, Rooney K, Levy MA, Relator R, Kerkhof J, McConkey H, Maas SM, Vissers LELM, de Vries BBA, Pfundt R, Elting MW, van Hagen JM, Verbeek NE, Jongmans MCJ, Lakeman P, Rumping L, Bosch DGM, Vitobello A, Thauvin-Robinet C, Faivre L, Nambot S, Garde A, Willems M, Genevieve D, Nicolas G, Busa T, Toutain A, Gérard M, Bizaoui V, Isidor B, Merla G, Accadia M, Schwartz CE, Ounap K, Hoffer MJV, Nezarati MM, van den Boogaard MH, Tedder ML, Rogers C, Brusco A, Ferrero GB, Spodenkiewicz M, Sidlow R, Mussa A, Trajkova S, McCann E, Mroczkowski HJ, Jansen S, Donker-Kaat L, Duijkers FAM, Stuurman KE, Mannens MMAM, Alders M, Henneman P, White SM, Sadikovic B, van Haelst MM. Vos N, et al. Among authors: tedder ml. Hum Genet. 2024 May 24. doi: 10.1007/s00439-024-02679-w. Online ahead of print. Hum Genet. 2024. PMID: 38787418
Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases.
Kerkhof J, Rastin C, Levy MA, Relator R, McConkey H, Demain L, Dominguez-Garrido E, Kaat LD, Houge SD, DuPont BR, Fee T, Fletcher RS, Gokhale D, Haukanes BI, Henneman P, Hilton S, Hilton BA, Jenkinson S, Lee JA, Louie RJ, Motazacker MM, Rzasa J, Stevenson RE, Plomp A, van der Laan L, van der Smagt J, Walden KK, Banka S, Mannens M, Skinner SA, Friez MJ, Campbell C, Tedder ML, Alders M, Sadikovic B. Kerkhof J, et al. Among authors: tedder ml. Genet Med. 2024 May;26(5):101075. doi: 10.1016/j.gim.2024.101075. Epub 2024 Jan 18. Genet Med. 2024. PMID: 38251460
Identification of DNA methylation episignature for the intellectual developmental disorder, autosomal dominant 21 syndrome, caused by variants in the CTCF gene.
Karimi K, Mol MO, Haghshenas S, Relator R, Levy MA, Kerkhof J, McConkey H, Brooks A, Zonneveld-Huijssoon E, Gerkes EH, Tedder ML, Vissers L, Salzano E, Piccione M, Asaftei SD, Carli D, Mussa A, Shukarova-Angelovska E, Trajkova S, Brusco A, Merla G, Alders MM, Bouman A, Sadikovic B. Karimi K, et al. Among authors: tedder ml. Genet Med. 2024 Mar;26(3):101041. doi: 10.1016/j.gim.2023.101041. Epub 2023 Dec 3. Genet Med. 2024. PMID: 38054406
Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.
Wang J, Foroutan A, Richardson E, Skinner SA, Reilly J, Kerkhof J, Curry CJ, Tarpey PS, Robertson SP, Maystadt I, Keren B, Dixon JW, Skinner C, Stapleton R, Ruaud L, Gumus E, Lakeman P, Alders M, Tedder ML, Schwartz CE, Friez MJ, Sadikovic B, Stevenson RE. Wang J, et al. Among authors: tedder ml. Eur J Hum Genet. 2023 Dec 1. doi: 10.1038/s41431-023-01499-2. Online ahead of print. Eur J Hum Genet. 2023. PMID: 38040915 No abstract available.
Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature.
LaFlamme CW, Rastin C, Sengupta S, Pennington HE, Russ-Hall SJ, Schneider AL, Bonkowski ES, Almanza Fuerte EP, Galey M, Goffena J, Gibson SB, Allan TJ, Nyaga DM, Lieffering N, Hebbar M, Walker EV, Darnell D, Olsen SR, Kolekar P, Djekidel N, Rosikiewicz W, McConkey H, Kerkhof J, Levy MA, Relator R, Lev D, Lerman-Sagie T, Park KL, Alders M, Cappuccio G, Chatron N, Demain L, Genevieve D, Lesca G, Roscioli T, Sanlaville D, Tedder ML, Hubshman MW, Ketkar S, Dai H, Worley KC, Rosenfeld JA, Chao HT; Undiagnosed Diseases Network; Neale G, Carvill GL; University of Washington Center for Rare Disease Research; Wang Z, Berkovic SF, Sadleir LG, Miller DE, Scheffer IE, Sadikovic B, Mefford HC. LaFlamme CW, et al. Among authors: tedder ml. medRxiv [Preprint]. 2023 Oct 12:2023.10.11.23296741. doi: 10.1101/2023.10.11.23296741. medRxiv. 2023. PMID: 37873138 Free PMC article. Preprint.
55 results