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

Year Number of Results
1968 3
1969 1
1970 3
1971 3
1972 1
1973 2
1974 3
1975 4
1976 5
1977 1
1978 4
1979 4
1980 3
1981 3
1982 6
1983 7
1984 4
1985 4
1986 5
1988 2
1989 4
1990 1
1991 2
1992 5
1993 3
1994 2
1995 6
1996 1
1997 5
1998 6
1999 2
2000 5
2001 1
2004 1
2006 1
2007 2
2008 1
2009 1
2010 5
2011 5
2012 4
2013 3
2014 3
2015 3
2016 1
2017 2
2018 1
2019 1
2020 2
2021 10
2022 6
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Search Results

157 results
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Page 1
The Boundaries of Critiquing a Colleague.
Rosenbaum KB, Rosmarin D. Rosenbaum KB, et al. J Am Acad Psychiatry Law. 2021 Dec;49(4):470-472. doi: 10.29158/JAAPL.210098-21. J Am Acad Psychiatry Law. 2021. PMID: 34903577 No abstract available.
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.
Koczkowska M, Chen Y, Callens T, Gomes A, Sharp A, Johnson S, Hsiao MC, Chen Z, Balasubramanian M, Barnett CP, Becker TA, Ben-Shachar S, Bertola DR, Blakeley JO, Burkitt-Wright EMM, Callaway A, Crenshaw M, Cunha KS, Cunningham M, D'Agostino MD, Dahan K, De Luca A, Destrée A, Dhamija R, Eoli M, Evans DGR, Galvin-Parton P, George-Abraham JK, Gripp KW, Guevara-Campos J, Hanchard NA, Hernández-Chico C, Immken L, Janssens S, Jones KJ, Keena BA, Kochhar A, Liebelt J, Martir-Negron A, Mahoney MJ, Maystadt I, McDougall C, McEntagart M, Mendelsohn N, Miller DT, Mortier G, Morton J, Pappas J, Plotkin SR, Pond D, Rosenbaum K, Rubin K, Russell L, Rutledge LS, Saletti V, Schonberg R, Schreiber A, Seidel M, Siqveland E, Stockton DW, Trevisson E, Ullrich NJ, Upadhyaya M, van Minkelen R, Verhelst H, Wallace MR, Yap YS, Zackai E, Zonana J, Zurcher V, Claes K, Martin Y, Korf BR, Legius E, Messiaen LM. Koczkowska M, et al. Among authors: rosenbaum k. Am J Hum Genet. 2018 Jan 4;102(1):69-87. doi: 10.1016/j.ajhg.2017.12.001. Epub 2017 Dec 28. Am J Hum Genet. 2018. PMID: 29290338 Free PMC article.
Anaphylactoid Syndrome of Pregnancy.
Barnhart ML, Rosenbaum K. Barnhart ML, et al. Among authors: rosenbaum k. Nurs Womens Health. 2019 Feb;23(1):38-48. doi: 10.1016/j.nwh.2018.11.006. Nurs Womens Health. 2019. PMID: 30738557
Missense variant contribution to USP9X-female syndrome.
Jolly LA, Parnell E, Gardner AE, Corbett MA, Pérez-Jurado LA, Shaw M, Lesca G, Keegan C, Schneider MC, Griffin E, Maier F, Kiss C, Guerin A, Crosby K, Rosenbaum K, Tanpaiboon P, Whalen S, Keren B, McCarrier J, Basel D, Sadedin S, White SM, Delatycki MB, Kleefstra T, Küry S, Brusco A, Sukarova-Angelovska E, Trajkova S, Yoon S, Wood SA, Piper M, Penzes P, Gecz J. Jolly LA, et al. Among authors: rosenbaum k. NPJ Genom Med. 2020 Dec 9;5(1):53. doi: 10.1038/s41525-020-00162-9. NPJ Genom Med. 2020. PMID: 33298948 Free PMC article.
Malignancy in Noonan syndrome and related disorders.
Smpokou P, Zand DJ, Rosenbaum KN, Summar ML. Smpokou P, et al. Among authors: rosenbaum kn. Clin Genet. 2015 Dec;88(6):516-22. doi: 10.1111/cge.12568. Epub 2015 Mar 4. Clin Genet. 2015. PMID: 25683281 Review.
Holoprosencephaly due to numeric chromosome abnormalities.
Solomon BD, Rosenbaum KN, Meck JM, Muenke M. Solomon BD, et al. Among authors: rosenbaum kn. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):146-8. doi: 10.1002/ajmg.c.30232. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104610 Free PMC article. Review.
Further delineation of the branchio-oculo-facial syndrome.
Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, et al. Lin AE, et al. Among authors: rosenbaum k. Am J Med Genet. 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. Am J Med Genet. 1995. PMID: 7747785 Free article. Review.
157 results