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Year Number of Results
1998 1
2014 2
2015 1
2017 4
2018 1
2019 1
2021 2
2022 4
2023 2
2024 0

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17 results

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Page 1
"Defensive Medicine" in the AI Era.
Banja J, Hollstein RD, Bruno MA. Banja J, et al. Among authors: hollstein rd. Eur J Radiol. 2023 Nov;168:111096. doi: 10.1016/j.ejrad.2023.111096. Epub 2023 Sep 16. Eur J Radiol. 2023. PMID: 37748324 No abstract available.
A Novel Frameshift CACNA1A Mutation Causing Episodic Ataxia Type 2.
Balck A, Tunc S, Schmitz J, Hollstein R, Kaiser FJ, Brüggemann N. Balck A, et al. Among authors: hollstein r. Cerebellum. 2018 Aug;17(4):504-506. doi: 10.1007/s12311-018-0931-8. Cerebellum. 2018. PMID: 29497979 No abstract available.
LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding.
Ludwig KU, Schmithausen RM, Li D, Jacobs ML, Hollstein R, Blumenstock K, Liebing J, Słabicki M, Ben-Shmuel A, Israeli O, Weiss S, Ebert TS, Paran N, Rüdiger W, Wilbring G, Feldman D, Lippke B, Ishorst N, Hochfeld LM, Beins EC, Kaltheuner IH, Schmitz M, Wöhler A, Döhla M, Sib E, Jentzsch M, Moench EC, Borrajo JD, Strecker J, Reinhardt J, Cleary B, Geyer M, Hölzel M, Macrae R, Nöthen MM, Hoffmann P, Exner M, Regev A, Zhang F, Schmid-Burgk JL. Ludwig KU, et al. Among authors: hollstein r. Nat Biotechnol. 2021 Dec;39(12):1556-1562. doi: 10.1038/s41587-021-00966-9. Epub 2021 Jun 29. Nat Biotechnol. 2021. PMID: 34188222 Free PMC article.
MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration.
Stüssel LG, Hollstein R, Laugsch M, Hochfeld LM, Welzenbach J, Schröder J, Thieme F, Ishorst N, Romero RO, Weinhold L, Hess T, Gehlen J, Mostowska A, Heilmann-Heimbach S, Mangold E, Rada-Iglesias A, Knapp M, Schaaf CP, Ludwig KU. Stüssel LG, et al. Among authors: hollstein r. J Dent Res. 2022 Mar;101(3):323-330. doi: 10.1177/00220345211038203. Epub 2021 Sep 16. J Dent Res. 2022. PMID: 34528480
Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding.
Ludwig KU, Schmithausen RM, Li D, Jacobs ML, Hollstein R, Blumenstock K, Liebing J, Słabicki M, Ben-Shmuel A, Israeli O, Weiss S, Ebert TS, Paran N, Rüdiger W, Wilbring G, Feldman D, Lippke B, Ishorst N, Hochfeld LM, Beins EC, Kaltheuner IH, Schmitz M, Wöhler A, Döhla M, Sib E, Jentzsch M, Moench EC, Borrajo JD, Strecker J, Reinhardt J, Cleary B, Geyer M, Hölzel M, Macrae R, Nöthen MM, Hoffmann P, Exner M, Regev A, Zhang F, Schmid-Burgk JL. Ludwig KU, et al. Among authors: hollstein r. Nat Biotechnol. 2022 Aug;40(8):1295. doi: 10.1038/s41587-022-01428-6. Nat Biotechnol. 2022. PMID: 35851378 Free PMC article. No abstract available.
HACE1 deficiency leads to structural and functional neurodevelopmental defects.
Nagy V, Hollstein R, Pai TP, Herde MK, Buphamalai P, Moeseneder P, Lenartowicz E, Kavirayani A, Korenke GC, Kozieradzki I, Nitsch R, Cicvaric A, Monje Quiroga FJ, Deardorff MA, Bedoukian EC, Li Y, Yigit G, Menche J, Perçin EF, Wollnik B, Henneberger C, Kaiser FJ, Penninger JM. Nagy V, et al. Among authors: hollstein r. Neurol Genet. 2019 Apr 29;5(3):e330. doi: 10.1212/NXG.0000000000000330. eCollection 2019 Jun. Neurol Genet. 2019. PMID: 31321300 Free PMC article.
HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome.
Hollstein R, Parry DA, Nalbach L, Logan CV, Strom TM, Hartill VL, Carr IM, Korenke GC, Uppal S, Ahmed M, Wieland T, Markham AF, Bennett CP, Gillessen-Kaesbach G, Sheridan EG, Kaiser FJ, Bonthron DT. Hollstein R, et al. J Med Genet. 2015 Dec;52(12):797-803. doi: 10.1136/jmedgenet-2015-103344. Epub 2015 Sep 30. J Med Genet. 2015. PMID: 26424145 Free PMC article.
17 results