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Items: 1 to 20 of 217

1.

Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene.

Vodo D, Sarig O, Geller S, Ben-Asher E, Olender T, Bochner R, Goldberg I, Nosgorodsky J, Alkelai A, Tatarskyy P, Peled A, Baum S, Barzilai A, Ibrahim SM, Zillikens D, Lancet D, Sprecher E.

PLoS Genet. 2016 May 5;12(5):e1006008. doi: 10.1371/journal.pgen.1006008. eCollection 2016 May.

2.

Genic insights from integrated human proteomics in GeneCards.

Fishilevich S, Zimmerman S, Kohn A, Iny Stein T, Olender T, Kolker E, Safran M, Lancet D.

Database (Oxford). 2016 Apr 5;2016. pii: baw030. doi: 10.1093/database/baw030. Print 2016.

3.

A role for TENM1 mutations in Congenital General Anosmia.

Alkelai A, Olender T, Haffner-Krausz R, Tsoory MM, Boyko V, Tatarskyy P, Gross-Isseroff R, Milgrom R, Shushan S, Blau I, Cohn E, Beeri R, Ephrat LL, Pras E, Lancet D.

Clin Genet. 2016 Apr 4. doi: 10.1111/cge.12782. [Epub ahead of print]

PMID:
27040985
4.

GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data.

Ben-Ari Fuchs S, Lieder I, Stelzer G, Mazor Y, Buzhor E, Kaplan S, Bogoch Y, Plaschkes I, Shitrit A, Rappaport N, Kohn A, Edgar R, Shenhav L, Safran M, Lancet D, Guan-Golan Y, Warshawsky D, Shtrichman R.

OMICS. 2016 Mar;20(3):139-51. doi: 10.1089/omi.2015.0168.

5.

TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability.

Heimer G, Oz-Levi D, Eyal E, Edvardson S, Nissenkorn A, Ruzzo EK, Szeinberg A, Maayan C, Mai-Zahav M, Efrati O, Pras E, Reznik-Wolf H, Lancet D, Goldstein DB, Anikster Y, Shalev SA, Elpeleg O, Ben Zeev B.

Eur J Paediatr Neurol. 2016 Jan;20(1):69-79. doi: 10.1016/j.ejpn.2015.10.003. Epub 2015 Oct 22.

PMID:
26542466
6.

Molecular disease presentation in diabetic nephropathy.

Heinzel A, Mühlberger I, Stelzer G, Lancet D, Oberbauer R, Martin M, Perco P.

Nephrol Dial Transplant. 2015 Aug;30 Suppl 4:iv17-25. doi: 10.1093/ndt/gfv267. Review.

PMID:
26209734
7.

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.

Heimer G, Marek-Yagel D, Eyal E, Barel O, Oz Levi D, Hoffmann C, Ruzzo EK, Ganelin-Cohen E, Lancet D, Pras E, Rechavi G, Nissenkorn A, Anikster Y, Goldstein DB, Ben Zeev B.

Clin Genet. 2015 Oct;88(4):327-35. doi: 10.1111/cge.12637. Epub 2015 Jul 28.

PMID:
26138499
8.

PathCards: multi-source consolidation of human biological pathways.

Belinky F, Nativ N, Stelzer G, Zimmerman S, Iny Stein T, Safran M, Lancet D.

Database (Oxford). 2015 Feb 27;2015. pii: bav006. doi: 10.1093/database/bav006. Print 2015.

9.

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.

Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, Ben-Zeev B, Nissenkorn A, Anikster Y, Oz-Levi D, Dhindsa RS, Hitomi Y, Schoch K, Spillmann RC, Heimer G, Marek-Yagel D, Tzadok M, Han Y, Worley G, Goldstein J, Jiang YH, Lancet D, Pras E, Shashi V, McHale D, Need AC, Goldstein DB.

Genet Med. 2015 Oct;17(10):774-81. doi: 10.1038/gim.2014.191. Epub 2015 Jan 15.

10.

Quasispecies in population of compositional assemblies.

Gross R, Fouxon I, Lancet D, Markovitch O.

BMC Evol Biol. 2014 Dec 30;14:265. doi: 10.1186/s12862-014-0265-1.

11.

Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome.

Oz-Levi D, Weiss B, Lahad A, Greenberger S, Pode-Shakked B, Somech R, Olender T, Tatarsky P, Marek-Yagel D, Pras E, Anikster Y, Lancet D.

Clin Genet. 2015 Jun;87(6):602-3. doi: 10.1111/cge.12494. Epub 2014 Oct 21. No abstract available.

PMID:
25335910
12.

MalaCards: A Comprehensive Automatically-Mined Database of Human Diseases.

Rappaport N, Twik M, Nativ N, Stelzer G, Bahir I, Stein TI, Safran M, Lancet D.

Curr Protoc Bioinformatics. 2014 Sep 8;47:1.24.1-19. doi: 10.1002/0471250953.bi0124s47.

PMID:
25199789
13.

Multispecies population dynamics of prebiotic compositional assemblies.

Markovitch O, Lancet D.

J Theor Biol. 2014 Sep 21;357:26-34. doi: 10.1016/j.jtbi.2014.05.005. Epub 2014 May 14.

PMID:
24831416
14.

The MATCHIT automaton: exploiting compartmentalization for the synthesis of branched polymers.

Weyland MS, Fellermann H, Hadorn M, Sorek D, Lancet D, Rasmussen S, Füchslin RM.

Comput Math Methods Med. 2013;2013:467428. doi: 10.1155/2013/467428. Epub 2013 Dec 31.

15.

Toward more transparent and reproducible omics studies through a common metadata checklist and data publications.

Kolker E, Özdemir V, Martens L, Hancock W, Anderson G, Anderson N, Aynacioglu S, Baranova A, Campagna SR, Chen R, Choiniere J, Dearth SP, Feng WC, Ferguson L, Fox G, Frishman D, Grossman R, Heath A, Higdon R, Hutz MH, Janko I, Jiang L, Joshi S, Kel A, Kemnitz JW, Kohane IS, Kolker N, Lancet D, Lee E, Li W, Lisitsa A, Llerena A, Macnealy-Koch C, Marshall JC, Masuzzo P, May A, Mias G, Monroe M, Montague E, Mooney S, Nesvizhskii A, Noronha S, Omenn G, Rajasimha H, Ramamoorthy P, Sheehan J, Smarr L, Smith CV, Smith T, Snyder M, Rapole S, Srivastava S, Stanberry L, Stewart E, Toppo S, Uetz P, Verheggen K, Voy BH, Warnich L, Wilhelm SW, Yandl G.

OMICS. 2014 Jan;18(1):10-4. doi: 10.1089/omi.2013.0149.

16.

MOPED enables discoveries through consistently processed proteomics data.

Higdon R, Stewart E, Stanberry L, Haynes W, Choiniere J, Montague E, Anderson N, Yandl G, Janko I, Broomall W, Fishilevich S, Lancet D, Kolker N, Kolker E.

J Proteome Res. 2014 Jan 3;13(1):107-13. doi: 10.1021/pr400884c. Epub 2013 Dec 18.

17.

Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy.

Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, Colleaux L, Décarie JC, Blaser S, Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ME, Aryal DK, Rodriguiz RM, Jiang YH, Wetsel WC, McNamara JO, Rouleau GA, Silver DL, Lancet D, Pras E, Mitchell GA, Michaud JL, Goldstein DB.

Neuron. 2013 Oct 16;80(2):429-41. doi: 10.1016/j.neuron.2013.08.013.

18.

Reproducibility: In praise of open research measures.

Kolker E, Altintas I, Bourne P, Faris J, Fox G, Frishman D, Geraci C, Hancock W, Lin B, Lancet D, Lisitsa A, Knight R, Martens L, Mesirov J, Özdemir V, Schultes E, Smith T, Snyder M, Srivastava S, Toppo S, Wilmes P.

Nature. 2013 Jun 13;498(7453):170. doi: 10.1038/498170b. No abstract available.

PMID:
23765483
19.

HORDE: comprehensive resource for olfactory receptor genomics.

Olender T, Nativ N, Lancet D.

Methods Mol Biol. 2013;1003:23-38. doi: 10.1007/978-1-62703-377-0_2.

PMID:
23585031
20.

MalaCards: an integrated compendium for diseases and their annotation.

Rappaport N, Nativ N, Stelzer G, Twik M, Guan-Golan Y, Stein TI, Bahir I, Belinky F, Morrey CP, Safran M, Lancet D.

Database (Oxford). 2013 Apr 12;2013:bat018. doi: 10.1093/database/bat018. Print 2013.

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