Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 39

1.

A multifaceted approach for analyzing complex phenotypic data in rodent models of autism.

Das I, Estevez MA, Sarkar AA, Banerjee-Basu S.

Mol Autism. 2019 Mar 12;10:11. doi: 10.1186/s13229-019-0263-7. eCollection 2019.

2.

AutDB: a platform to decode the genetic architecture of autism.

Pereanu W, Larsen EC, Das I, Estévez MA, Sarkar AA, Spring-Pearson S, Kollu R, Basu SN, Banerjee-Basu S.

Nucleic Acids Res. 2018 Jan 4;46(D1):D1049-D1054. doi: 10.1093/nar/gkx1093.

3.

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.

Larsen E, Menashe I, Ziats MN, Pereanu W, Packer A, Banerjee-Basu S.

Mol Autism. 2016 Oct 21;7:44. doi: 10.1186/s13229-016-0103-y. eCollection 2016.

4.

Common microRNAs Target Established ASD Genes.

Banerjee-Basu S, Larsen E, Muend S.

Front Neurol. 2014 Oct 28;5:205. doi: 10.3389/fneur.2014.00205. eCollection 2014. Review. No abstract available.

5.

STX1A and Asperger syndrome: a replication study.

Durdiaková J, Warrier V, Banerjee-Basu S, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2014 Feb 18;5(1):14. doi: 10.1186/2040-2392-5-14.

6.

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.

Mol Autism. 2013 Oct 3;4(1):36. doi: 10.1186/2040-2392-4-36.

7.

Co-expression profiling of autism genes in the mouse brain.

Menashe I, Grange P, Larsen EC, Banerjee-Basu S, Mitra PP.

PLoS Comput Biol. 2013;9(7):e1003128. doi: 10.1371/journal.pcbi.1003128. Epub 2013 Jul 25.

8.

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.

Menashe I, Larsen EC, Banerjee-Basu S.

PLoS One. 2013 Jun 18;8(6):e66707. doi: 10.1371/journal.pone.0066707. Print 2013.

9.

A brain region-specific predictive gene map for autism derived by profiling a reference gene set.

Kumar A, Swanwick CC, Johnson N, Menashe I, Basu SN, Bales ME, Banerjee-Basu S.

PLoS One. 2011;6(12):e28431. doi: 10.1371/journal.pone.0028431. Epub 2011 Dec 9.

10.

Animal model integration to AutDB, a genetic database for autism.

Kumar A, Wadhawan R, Swanwick CC, Kollu R, Basu SN, Banerjee-Basu S.

BMC Med Genomics. 2011 Jan 27;4:15. doi: 10.1186/1755-8794-4-15.

11.

SFARI Gene: an evolving database for the autism research community.

Banerjee-Basu S, Packer A.

Dis Model Mech. 2010 Mar-Apr;3(3-4):133-5. doi: 10.1242/dmm.005439. No abstract available.

12.

Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome.

Chakrabarti B, Dudbridge F, Kent L, Wheelwright S, Hill-Cawthorne G, Allison C, Banerjee-Basu S, Baron-Cohen S.

Autism Res. 2009 Jun;2(3):157-77. doi: 10.1002/aur.80.

PMID:
19598235
13.

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.

Roessler E, Pei W, Ouspenskaia MV, Karkera JD, Veléz JI, Banerjee-Basu S, Gibney G, Lupo PJ, Mitchell LE, Towbin JA, Bowers P, Belmont JW, Goldmuntz E, Baxevanis AD, Feldman B, Muenke M.

Mol Genet Metab. 2009 Sep-Oct;98(1-2):225-34. doi: 10.1016/j.ymgme.2009.05.005. Epub 2009 May 27.

14.

AutDB: a gene reference resource for autism research.

Basu SN, Kollu R, Banerjee-Basu S.

Nucleic Acids Res. 2009 Jan;37(Database issue):D832-6. doi: 10.1093/nar/gkn835. Epub 2008 Nov 10.

15.

Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans.

Karkera JD, Lee JS, Roessler E, Banerjee-Basu S, Ouspenskaia MV, Mez J, Goldmuntz E, Bowers P, Towbin J, Belmont JW, Baxevanis AD, Schier AF, Muenke M.

Am J Hum Genet. 2007 Nov;81(5):987-94. Epub 2007 Sep 28.

16.

Gaucher mutation N188S is associated with myoclonic epilepsy.

Kowarz L, Goker-Alpan O, Banerjee-Basu S, LaMarca ME, Kinlaw L, Schiffmann R, Baxevanis AD, Sidransky E.

Hum Mutat. 2005 Sep;26(3):271-3; author reply 274-5.

PMID:
16086325
17.

The zebrafish gene claudinj is essential for normal ear function and important for the formation of the otoliths.

Hardison AL, Lichten L, Banerjee-Basu S, Becker TS, Burgess SM.

Mech Dev. 2005 Jul;122(7-8):949-58.

18.

Essential structural and functional determinants within the forkhead domain of FOXC1.

Saleem RA, Banerjee-Basu S, Murphy TC, Baxevanis A, Walter MA.

Nucleic Acids Res. 2004 Aug 6;32(14):4182-93. Print 2004.

19.

Structural analysis of disease-causing mutations in the P-subfamily of forkhead transcription factors.

Banerjee-Basu S, Baxevanis AD.

Proteins. 2004 Mar 1;54(4):639-47.

PMID:
14997560
20.

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.

Saleem RA, Banerjee-Basu S, Berry FB, Baxevanis AD, Walter MA.

Hum Mol Genet. 2003 Nov 15;12(22):2993-3005. Epub 2003 Sep 23.

PMID:
14506133
21.

The Homeodomain Resource: 2003 update.

Banerjee-Basu S, Moreland T, Hsu BJ, Trout KL, Baxevanis AD.

Nucleic Acids Res. 2003 Jan 1;31(1):304-6.

22.

Molecular modeling of mutations in the DNA-binding domain of the oncoprotein Qin.

Banerjee-Basu S, Baxevanis AD.

Mol Cancer Ther. 2002 Nov;1(13):1237-41.

23.

The DNA-binding region of RAG 1 is not a homeodomain.

Banerjee-Basu S, Baxevanis AD.

Genome Biol. 2002 Jul 25;3(8):INTERACTIONS1004. Epub 2002 Jul 25. Review.

24.

Threading analysis of prospero-type homeodomains.

Banerjee-Basu S, Landsman D, Baxevanis AD.

In Silico Biol. 1999;1(3):163-73.

PMID:
11471237
25.

Molecular evolution of the homeodomain family of transcription factors.

Banerjee-Basu S, Baxevanis AD.

Nucleic Acids Res. 2001 Aug 1;29(15):3258-69.

26.

Predictive methods using protein sequences.

Banerjee-Basu S, Baxevanis AD.

Methods Biochem Anal. 2001;43:253-82. No abstract available.

PMID:
11449728
27.

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1.

Saleem RA, Banerjee-Basu S, Berry FB, Baxevanis AD, Walter MA.

Am J Hum Genet. 2001 Mar;68(3):627-41.

28.

Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome.

Stone DL, Slavotinek A, Bouffard GG, Banerjee-Basu S, Baxevanis AD, Barr M, Biesecker LG.

Nat Genet. 2000 May;25(1):79-82.

PMID:
10802661
29.

The Homeodomain Resource: sequences, structures, DNA binding sites and genomic information.

Banerjee-Basu S, Sink DW, Baxevanis AD.

Nucleic Acids Res. 2001 Jan 1;29(1):291-3.

30.

MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability.

Lipkin SM, Wang V, Jacoby R, Banerjee-Basu S, Baxevanis AD, Lynch HT, Elliott RM, Collins FS.

Nat Genet. 2000 Jan;24(1):27-35.

PMID:
10615123
31.

The homeodomain resource: a prototype database for a large protein family.

Banerjee-Basu S, Ryan JF, Baxevanis AD.

Nucleic Acids Res. 2000 Jan 1;28(1):329-30.

33.

The Homeodomain Resource: sequences, structures and genomic information.

Banerjee-Basu S, Ferlanti ES, Ryan JF, Baxevanis AD.

Nucleic Acids Res. 1999 Jan 1;27(1):336-7.

34.

Chicken homeobox gene Prox 1 related to Drosophila prospero is expressed in the developing lens and retina.

Tomarev SI, Sundin O, Banerjee-Basu S, Duncan MK, Yang JM, Piatigorsky J.

Dev Dyn. 1996 Aug;206(4):354-67. Erratum in: Dev Dyn 1996 Sep;207(1):120.

35.

Sequence and expression of chicken betaA2- and betaB3 crystallins.

Duncan MK, Banerjee-Basu S, McDermott JB, Piatugorsky J.

Exp Eye Res. 1996 Jun;62(6):721-2. No abstract available.

PMID:
8983953
36.

Common core sequences are found in skeletal muscle slow- and fast-fiber-type-specific regulatory elements.

Nakayama M, Stauffer J, Cheng J, Banerjee-Basu S, Wawrousek E, Buonanno A.

Mol Cell Biol. 1996 May;16(5):2408-17.

37.

Sequence and expression of chicken beta A2- and beta B3-crystallins.

Duncan MK, Banerjee-Basu S, McDermott JB, Piatigorsky J.

Exp Eye Res. 1996 Jan;62(1):111-9.

PMID:
8674507
38.

Isolation and structure of the rat gene encoding troponin I(slow).

Banerjee-Basu S, Buonanno A.

Gene. 1994 Aug 5;145(2):241-4.

PMID:
8056338

Supplemental Content

Loading ...
Support Center