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

Year Number of Results
1950 1
1971 1
1972 1
1986 1
1987 1
1990 1
1994 1
2004 2
2005 3
2006 2
2008 2
2009 3
2010 3
2011 4
2012 6
2013 7
2014 7
2015 5
2016 5
2017 6
2018 6
2019 5
2021 2
2022 7
2023 3
2024 0

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70 results

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Page 1
What's the hype about CDK5RAP2?
Kraemer N, Issa L, Hauck SC, Mani S, Ninnemann O, Kaindl AM. Kraemer N, et al. Cell Mol Life Sci. 2011 May;68(10):1719-36. doi: 10.1007/s00018-011-0635-4. Epub 2011 Feb 17. Cell Mol Life Sci. 2011. PMID: 21327915 Review.
Proteome changes in autosomal recessive primary microcephaly.
Zaqout S, Mannaa A, Klein O, Krajewski A, Klose J, Luise-Becker L, Elsabagh A, Ferih K, Kraemer N, Ravindran E, Makridis K, Kaindl AM. Zaqout S, et al. Among authors: kraemer n. Ann Hum Genet. 2023 Mar;87(1-2):50-62. doi: 10.1111/ahg.12489. Epub 2022 Nov 29. Ann Hum Genet. 2023. PMID: 36448252
Many roads lead to primary autosomal recessive microcephaly.
Kaindl AM, Passemard S, Kumar P, Kraemer N, Issa L, Zwirner A, Gerard B, Verloes A, Mani S, Gressens P. Kaindl AM, et al. Among authors: kraemer n. Prog Neurobiol. 2010 Mar;90(3):363-83. doi: 10.1016/j.pneurobio.2009.11.002. Epub 2009 Dec 2. Prog Neurobiol. 2010. PMID: 19931588 Review.
Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.
Picker-Minh S, Hartenstein S, Proquitté H, Fröhler S, Raile V, Kraemer N, Apeshiotis S, Leipoldt M, Kalache KD, Morris-Rosendahl D, Boltshauser E, Chen W, Kaindl AM. Picker-Minh S, et al. Among authors: kraemer n. J Child Neurol. 2017 Mar;32(3):334-340. doi: 10.1177/0883073816680748. Epub 2016 Dec 20. J Child Neurol. 2017. PMID: 28193110 Review.
Novel Alternative Splice Variants of Mouse Cdk5rap2.
Kraemer N, Issa-Jahns L, Neubert G, Ravindran E, Mani S, Ninnemann O, Kaindl AM. Kraemer N, et al. PLoS One. 2015 Aug 31;10(8):e0136684. doi: 10.1371/journal.pone.0136684. eCollection 2015. PLoS One. 2015. PMID: 26322982 Free PMC article.
Genetic causes of MCPH in consanguineous Pakistani families.
Kraemer N, Picker-Minh S, Abbasi AA, Fröhler S, Ninnemann O, Khan MN, Ali G, Chen W, Kaindl AM. Kraemer N, et al. Clin Genet. 2016 Jun;89(6):744-5. doi: 10.1111/cge.12685. Epub 2015 Nov 8. Clin Genet. 2016. PMID: 26548919 No abstract available.
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation.
Ravindran E, Hu H, Yuzwa SA, Hernandez-Miranda LR, Kraemer N, Ninnemann O, Musante L, Boltshauser E, Schindler D, Hübner A, Reinecker HC, Ropers HH, Birchmeier C, Miller FD, Wienker TF, Hübner C, Kaindl AM. Ravindran E, et al. Among authors: kraemer n. PLoS Genet. 2017 Apr 28;13(4):e1006746. doi: 10.1371/journal.pgen.1006746. eCollection 2017 Apr. PLoS Genet. 2017. PMID: 28453519 Free PMC article.
70 results