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Results by year

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

Year Number of Results
1954 1
1955 1
1958 1
1961 3
1964 1
1965 3
1966 1
1967 1
1970 2
1971 3
1973 2
1974 1
1975 1
1977 3
1978 1
1981 3
1982 1
1983 3
1985 7
1987 4
1989 3
1990 2
1991 2
1992 3
1993 6
1994 2
1995 11
1996 3
1997 6
1998 1
1999 11
2000 6
2001 7
2002 17
2003 7
2004 14
2005 8
2006 12
2007 13
2008 13
2009 7
2010 9
2011 6
2012 5
2013 11
2014 12
2015 7
2016 10
2017 12
2018 4
2019 7
2020 3
2021 8
2022 8
2023 4
2024 2

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Search Results

281 results

Results by year

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Page 1
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A; CAUSES Study; Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K; SPARK Consortium; Earl RK, Nowakowski T, Bernier RA, Eichler EE. Gillentine MA, et al. Among authors: hansen lk. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. Genome Med. 2021. PMID: 33874999 Free PMC article.
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.
Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez-Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärtner J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, Smith-Hicks CL, Hino-Fukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM. Zagaglia S, et al. Among authors: hansen lk. Neurology. 2018 Nov 27;91(22):e2078-e2088. doi: 10.1212/WNL.0000000000006567. Epub 2018 Nov 9. Neurology. 2018. PMID: 30413629 Free PMC article.
[Sarcoidosis].
Kammerlander H, Hansen LK. Kammerlander H, et al. Among authors: hansen lk. Ugeskr Laeger. 2014 Mar 3;176(5):V63813. Ugeskr Laeger. 2014. PMID: 25096014 Free article. Danish. No abstract available.
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.
Oppermann H, Marcos-Grañeda E, Weiss LA, Gurnett CA, Jelsig AM, Vineke SH, Isidor B, Mercier S, Magnussen K, Zacher P, Hashim M, Pagnamenta AT, Race S, Srivastava S, Frazier Z, Maiwald R, Pergande M, Milani D, Rinelli M, Levy J, Krey I, Fontana P, Lonardo F, Riley S, Kretzer J, Rankin J, Reis LM, Semina EV, Reuter MS, Scherer SW, Iascone M, Weis D, Fagerberg CR, Brasch-Andersen C, Hansen LK, Kuechler A, Noble N, Gardham A, Tenney J, Rathore G, Beck-Woedl S, Haack TB, Pavlidou DC, Atallah I, Vodopiutz J, Janecke AR, Hsieh TC, Lesmann H, Klinkhammer H, Krawitz PM, Lemke JR, Jamra RA, Nieto M, Tümer Z, Platzer K. Oppermann H, et al. Among authors: hansen lk. Eur J Hum Genet. 2023 Nov;31(11):1251-1260. doi: 10.1038/s41431-023-01445-2. Epub 2023 Aug 30. Eur J Hum Genet. 2023. PMID: 37644171 Free PMC article.
Modulation transfer functions for audiovisual speech.
Pedersen NF, Dau T, Hansen LK, Hjortkjær J. Pedersen NF, et al. Among authors: hansen lk. PLoS Comput Biol. 2022 Jul 19;18(7):e1010273. doi: 10.1371/journal.pcbi.1010273. eCollection 2022 Jul. PLoS Comput Biol. 2022. PMID: 35852989 Free PMC article.
Process mapping strategies to prevent subcutaneous implantable cardioverter-defibrillator infections.
Weiss R, Mark GE, El-Chami MF, Biffi M, Probst V, Lambiase PD, Miller MA, McClernon T, Hansen LK, Knight BP, Baddour LM; other members of the S-ICD Process Mapping Consortium. Weiss R, et al. Among authors: hansen lk. J Cardiovasc Electrophysiol. 2022 Jul;33(7):1628-1635. doi: 10.1111/jce.15566. Epub 2022 Jun 9. J Cardiovasc Electrophysiol. 2022. PMID: 35662315 Free PMC article. Review.
Biclique communities.
Lehmann S, Schwartz M, Hansen LK. Lehmann S, et al. Among authors: hansen lk. Phys Rev E Stat Nonlin Soft Matter Phys. 2008 Jul;78(1 Pt 2):016108. doi: 10.1103/PhysRevE.78.016108. Epub 2008 Jul 21. Phys Rev E Stat Nonlin Soft Matter Phys. 2008. PMID: 18764021 Free article.
fMRI neuroinformatics.
Nielsen FA, Christensen MS, Madsen KH, Lund TE, Hansen LK. Nielsen FA, et al. Among authors: hansen lk. IEEE Eng Med Biol Mag. 2006 Mar-Apr;25(2):112-9. doi: 10.1109/memb.2006.1607675. IEEE Eng Med Biol Mag. 2006. PMID: 16568943 Free article. Review. No abstract available.
Corroles cannot ruffle.
Thomas KE, Conradie J, Hansen LK, Ghosh A. Thomas KE, et al. Among authors: hansen lk. Inorg Chem. 2011 Apr 18;50(8):3247-51. doi: 10.1021/ic1017032. Epub 2011 Mar 2. Inorg Chem. 2011. PMID: 21366225
281 results