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Items: 1 to 50 of 312

1.

Neural correlates of theory-of-mind are associated with variation in children's everyday social cognition.

Mukerji CE, Lincoln SH, Dodell-Feder D, Nelson CA, Hooker CI.

Soc Cogn Affect Neurosci. 2019 Jun 13. pii: nsz040. doi: 10.1093/scan/nsz040. [Epub ahead of print]

PMID:
31194250
2.

Comprehensive Analysis of Aspergillus nidulans PKA Phosphorylome Identifies a Novel Mode of CreA Regulation.

Ribeiro LFC, Chelius C, Boppidi KR, Naik NS, Hossain S, Ramsey JJJ, Kumar J, Ribeiro LF, Ostermeier M, Tran B, Ah Goo Y, de Assis LJ, Ulas M, Bayram O, Goldman GH, Lincoln S, Srivastava R, Harris SD, Marten MR.

MBio. 2019 Apr 30;10(2). pii: e02825-18. doi: 10.1128/mBio.02825-18.

3.

Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.

Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, Datar C, Verma IC, Puri RD, Zollino M, Bachmann-Gagescu R, Niedrist D, Papik M, Figueiro-Silva J, Masood R, Zweier M, Kraemer D, Lincoln S, Rodan L; Undiagnosed Diseases Network (UDN), Passemard S, Drunat S, Verloes A, Horn AHC, Sticht H, Steinfeld R, Plecko B, Latal B, Jenni O, Asadollahi R, Rauch A.

Genet Med. 2019 Mar 7. doi: 10.1038/s41436-019-0464-7. [Epub ahead of print]

PMID:
30842647
4.

Phosphoproteomic and transcriptomic analyses reveal multiple functions for Aspergillus nidulans MpkA independent of cell wall stress.

Chelius CL, Ribeiro LFC, Huso W, Kumar J, Lincoln S, Tran B, Goo YA, Srivastava R, Harris SD, Marten MR.

Fungal Genet Biol. 2019 Apr;125:1-12. doi: 10.1016/j.fgb.2019.01.003. Epub 2019 Jan 9.

PMID:
30639305
5.

A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing.

Lincoln SE, Truty R, Lin CF, Zook JM, Paul J, Ramey VH, Salit M, Rehm HL, Nussbaum RL, Lebo MS.

J Mol Diagn. 2019 Mar;21(2):318-329. doi: 10.1016/j.jmoldx.2018.10.009. Epub 2019 Jan 3.

6.

Altered reward processing following an acute social stressor in adolescents.

Lincoln SH, Pisoni A, Bondy E, Kumar P, Singleton P, Hajcak G, Pizzagalli DA, Auerbach RP.

PLoS One. 2019 Jan 4;14(1):e0209361. doi: 10.1371/journal.pone.0209361. eCollection 2019.

7.

Non-Suicidal self-injury and suicide in depressed Adolescents: Impact of peer victimization and bullying.

Vergara GA, Stewart JG, Cosby EA, Lincoln SH, Auerbach RP.

J Affect Disord. 2019 Feb 15;245:744-749. doi: 10.1016/j.jad.2018.11.084. Epub 2018 Nov 13.

PMID:
30448758
8.

ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans.

Conway OJ, Carrasquillo MM, Wang X, Bredenberg JM, Reddy JS, Strickland SL, Younkin CS, Burgess JD, Allen M, Lincoln SJ, Nguyen T, Malphrus KG, Soto AI, Walton RL, Boeve BF, Petersen RC, Lucas JA, Ferman TJ, Cheshire WP, van Gerpen JA, Uitti RJ, Wszolek ZK, Ross OA, Dickson DW, Graff-Radford NR, Ertekin-Taner N.

Mol Neurodegener. 2018 Oct 11;13(1):53. doi: 10.1186/s13024-018-0289-x.

9.

Viable cyanobacteria in the deep continental subsurface.

Puente-Sánchez F, Arce-Rodríguez A, Oggerin M, García-Villadangos M, Moreno-Paz M, Blanco Y, Rodríguez N, Bird L, Lincoln SA, Tornos F, Prieto-Ballesteros O, Freeman KH, Pieper DH, Timmis KN, Amils R, Parro V.

Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):10702-10707. doi: 10.1073/pnas.1808176115. Epub 2018 Oct 1.

10.

Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy.

Allen M, Wang X, Serie DJ, Strickland SL, Burgess JD, Koga S, Younkin CS, Nguyen TT, Malphrus KG, Lincoln SJ, Alamprese M, Zhu K, Chang R, Carrasquillo MM, Kouri N, Murray ME, Reddy JS, Funk C, Price ND, Golde TE, Younkin SG, Asmann YW, Crook JE, Dickson DW, Ertekin-Taner N.

Acta Neuropathol. 2018 Nov;136(5):709-727. doi: 10.1007/s00401-018-1900-5. Epub 2018 Aug 22.

11.

An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery.

Haghighi A, Krier JB, Toth-Petroczy A, Cassa CA, Frank NY, Carmichael N, Fieg E, Bjonnes A, Mohanty A, Briere LC, Lincoln S, Lucia S, Gupta VA, Söylemez O, Sutti S, Kooshesh K, Qiu H, Fay CJ, Perroni V, Valerius J, Hanna M, Frank A, Ouahed J, Snapper SB, Pantazi A, Chopra SS, Leshchiner I, Stitziel NO, Feldweg A, Mannstadt M, Loscalzo J, Sweetser DA, Liao E, Stoler JM, Nowak CB, Sanchez-Lara PA, Klein OD, Perry H, Patsopoulos NA, Raychaudhuri S, Goessling W, Green RC, Seidman CE, MacRae CA, Sunyaev SR, Maas RL, Vuzman D; Undiagnosed Diseases Network, Brigham and Women’s Hospital FaceBase Project, Brigham Genomic Medicine (BGM).

NPJ Genom Med. 2018 Aug 13;3:21. doi: 10.1038/s41525-018-0060-9. eCollection 2018. Review.

12.

Molecular tweezers with a rotationally restricted linker and freely rotating porphyrin moieties.

Murphy RB, Pham DT, White JM, Lincoln SF, Johnston MR.

Org Biomol Chem. 2018 Aug 29;16(34):6206-6223. doi: 10.1039/c8ob00944a.

PMID:
30106402
13.

Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomes.

Whitley BN, Lam C, Cui H, Haude K, Bai R, Escobar L, Hamilton A, Brady L, Tarnopolsky MA, Dengle L, Picker J, Lincoln S, Lackner LL, Glass IA, Hoppins S.

Hum Mol Genet. 2018 Nov 1;27(21):3710-3719. doi: 10.1093/hmg/ddy287.

PMID:
30085106
14.

An alternative transcript of the Alzheimer's disease risk gene SORL1 encodes a truncated receptor.

Blechingberg J, Poulsen ASA, Kjølby M, Monti G, Allen M, Ivarsen AK, Lincoln SJ, Thotakura G, Vægter CB, Ertekin-Taner N, Nykjær A, Andersen OM.

Neurobiol Aging. 2018 Nov;71:266.e11-266.e24. doi: 10.1016/j.neurobiolaging.2018.06.021. Epub 2018 Jun 28.

PMID:
30078640
15.

Social impairment and social language deficits in children and adolescents with and at risk for psychosis.

D'Angelo EJ, Morelli N, Lincoln SH, Graber K, Tembulkar S, Gaudet A, Gonzalez-Heydrich J.

Schizophr Res. 2019 Feb;204:304-310. doi: 10.1016/j.schres.2018.07.028. Epub 2018 Aug 1.

PMID:
30077431
16.

Altered secretion patterns and cell wall organization caused by loss of PodB function in the filamentous fungus Aspergillus nidulans.

Boppidi KR, Ribeiro LFC, Iambamrung S, Nelson SM, Wang Y, Momany M, Richardson EA, Lincoln S, Srivastava R, Harris SD, Marten MR.

Sci Rep. 2018 Jul 30;8(1):11433. doi: 10.1038/s41598-018-29615-z.

17.

Underdiagnosis of Hereditary Breast and Ovarian Cancer in Medicare Patients: Genetic Testing Criteria Miss the Mark.

Yang S, Axilbund JE, O'Leary E, Michalski ST, Evans R, Lincoln SE, Esplin ED, Nussbaum RL.

Ann Surg Oncol. 2018 Oct;25(10):2925-2931. doi: 10.1245/s10434-018-6621-4. Epub 2018 Jul 11.

PMID:
29998407
18.

The influence of pressure on crude oil biodegradation in shallow and deep Gulf of Mexico sediments.

Nguyen UT, Lincoln SA, Valladares Juárez AG, Schedler M, Macalady JL, Müller R, Freeman KH.

PLoS One. 2018 Jul 3;13(7):e0199784. doi: 10.1371/journal.pone.0199784. eCollection 2018.

19.

De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome.

Torres A, Brownstein CA, Tembulkar SK, Graber K, Genetti C, Kleiman RJ, Sweadner KJ, Mavros C, Liu KX, Smedemark-Margulies N, Maski K, Yang E, Agrawal PB, Shi J, Beggs AH, D'Angelo E, Lincoln SH, Carroll D, Dedeoglu F, Gahl WA, Biggs CM, Swoboda KJ, Berry GT, Gonzalez-Heydrich J.

Mol Genet Metab Rep. 2018 Jun 15;16:23-29. doi: 10.1016/j.ymgmr.2018.06.001. eCollection 2018 Sep.

20.

Prevalence and properties of intragenic copy-number variation in Mendelian disease genes.

Truty R, Paul J, Kennemer M, Lincoln SE, Olivares E, Nussbaum RL, Aradhya S.

Genet Med. 2019 Jan;21(1):114-123. doi: 10.1038/s41436-018-0033-5. Epub 2018 Jun 12.

PMID:
29895855
21.

Low-abundant bacteria drive compositional changes in the gut microbiota after dietary alteration.

Benjamino J, Lincoln S, Srivastava R, Graf J.

Microbiome. 2018 May 10;6(1):86. doi: 10.1186/s40168-018-0469-5.

22.

Potentially traumatic events in youth with and at clinical high risk for psychosis.

Morelli N, Fogler J, Tembulkar S, Graber K, Lincoln SH, Bosquet Enlow M, Gonzalez-Heydrich J, D'Angelo EJ.

Early Interv Psychiatry. 2019 Aug;13(4):805-809. doi: 10.1111/eip.12565. Epub 2018 Mar 25.

PMID:
29575640
23.

Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network.

Palmer CGS, McConkie-Rosell A, Holm IA, LeBlanc K, Sinsheimer JS, Briere LC, Dorrani N, Herzog MR, Lincoln S, Schoch K, Spillmann RC, Brokamp E; Undiagnosed Diseases Network.

J Genet Couns. 2018 Sep;27(5):1087-1101. doi: 10.1007/s10897-018-0228-6. Epub 2018 Mar 1.

24.

Germline mutation prevalence in individuals with pancreatic cancer and a history of previous malignancy.

Dudley B, Karloski E, Monzon FA, Singhi AD, Lincoln SE, Bahary N, Brand RE.

Cancer. 2018 Apr 15;124(8):1691-1700. doi: 10.1002/cncr.31242. Epub 2018 Jan 23.

25.

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.

Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, Churchhouse C, Fontanillas P, King R, Lee S, Lincoln SE, Trubetskoy V, DePristo M, Fingerlin T, Grossman R, Grundstad J, Heath A, Kim J, Kim YJ, Laramie J, Lee J, Li H, Liu X, Livne O, Locke AE, Maller J, Mazur A, Morris AP, Pollin TI, Ragona D, Reich D, Rivas MA, Scott LJ, Sim X, Tearle RG, Teo YY, Williams AL, Zöllner S, Curran JE, Peralta J, Akolkar B, Bell GI, Burtt NP, Cox NJ, Florez JC, Hanis CL, McKeon C, Mohlke KL, Seielstad M, Wilson JG, Atzmon G, Below JE, Dupuis J, Nicolae DL, Lehman D, Park T, Won S, Sladek R, Altshuler D, McCarthy MI, Duggirala R, Boehnke M, Frayling TM, Abecasis GR, Blangero J.

Proc Natl Acad Sci U S A. 2018 Jan 9;115(2):379-384. doi: 10.1073/pnas.1705859115. Epub 2017 Dec 26.

26.

Corrigendum: Sources of discordance among germ-line variant classifications in ClinVar.

Yang S, Lincoln SE, Kobayashi Y, Nykamp K, Nussbaum RL, Topper S.

Genet Med. 2018 Feb;20(2):282. doi: 10.1038/gim.2017.198. Epub 2017 Dec 7.

PMID:
29215652
27.

Neural simulation mechanisms and social-emotional function in schizophrenia.

Mukerji CE, Lincoln SH, Tully LM, Dodell-Feder D, Hooker CI.

Psychiatry Res Neuroimaging. 2018 Jan 30;271:34-42. doi: 10.1016/j.pscychresns.2017.10.006. Epub 2017 Oct 24.

PMID:
29174437
28.

Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists.

Roy S, Coldren C, Karunamurthy A, Kip NS, Klee EW, Lincoln SE, Leon A, Pullambhatla M, Temple-Smolkin RL, Voelkerding KV, Wang C, Carter AB.

J Mol Diagn. 2018 Jan;20(1):4-27. doi: 10.1016/j.jmoldx.2017.11.003. Epub 2017 Nov 21. Review.

PMID:
29154853
29.

Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases.

Allen M, Wang X, Burgess JD, Watzlawik J, Serie DJ, Younkin CS, Nguyen T, Malphrus KG, Lincoln S, Carrasquillo MM, Ho C, Chakrabarty P, Strickland S, Murray ME, Swarup V, Geschwind DH, Seyfried NT, Dammer EB, Lah JJ, Levey AI, Golde TE, Funk C, Li H, Price ND, Petersen RC, Graff-Radford NR, Younkin SG, Dickson DW, Crook JR, Asmann YW, Ertekin-Taner N.

Alzheimers Dement. 2018 Mar;14(3):352-366. doi: 10.1016/j.jalz.2017.09.012. Epub 2017 Oct 31.

30.

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, Denommé-Pichon AS, Lesca G, Sellars EA, Berg J, Carré W, Busk ØL, van Bon BWM, Waugh JL, Deardorff M, Hoganson GE, Bosanko KB, Johnson DS, Dabir T, Holla ØL, Sarkar A, Tveten K, de Bellescize J, Braathen GJ, Terhal PA, Grange DK, van Haeringen A, Lam C, Mirzaa G, Burton J, Bhoj EJ, Douglas J, Santani AB, Nesbitt AI, Helbig KL, Andrews MV, Begtrup A, Tang S, van Gassen KLI, Juusola J, Foss K, Enns GM, Moog U, Hinderhofer K, Paramasivam N, Lincoln S, Kusako BH, Lindenbaum P, Charpentier E, Nowak CB, Cherot E, Simonet T, Ruivenkamp CAL, Hahn S, Brownstein CA, Xia F, Schmitt S, Deb W, Bonneau D, Nizon M, Quinquis D, Chelly J, Rudolf G, Sanlaville D, Parent P, Gilbert-Dussardier B, Toutain A, Sutton VR, Thies J, Peart-Vissers LELM, Boisseau P, Vincent M, Grabrucker AM, Dubourg C; Undiagnosed Diseases Network, Tan WH, Verbeek NE, Granzow M, Santen GWE, Shendure J, Isidor B, Pasquier L, Redon R, Yang Y, State MW, Kleefstra T, Cogné B; GEM HUGO; Deciphering Developmental Disorders Study, Petrovski S, Retterer K, Eichler EE, Rosenfeld JA, Agrawal PB, Bézieau S, Odent S, Elgersma Y, Mercier S.

Am J Hum Genet. 2017 Nov 2;101(5):768-788. doi: 10.1016/j.ajhg.2017.10.003.

31.

β-Cyclodextrin- and adamantyl-substituted poly(acrylate) self-assembling aqueous networks designed for controlled complexation and release of small molecules.

Yan L, Pham DT, Clements P, Lincoln SF, Wang J, Guo X, Easton CJ.

Beilstein J Org Chem. 2017 Sep 7;13:1879-1892. doi: 10.3762/bjoc.13.183. eCollection 2017.

32.

Solvent Effects on the Intramolecular Charge Transfer Character of N,N-Diaryl Dihydrophenazine Catalysts for Organocatalyzed Atom Transfer Radical Polymerization.

Ryan MD, Theriot JC, Lim CH, Yang H, Lockwood A, Garrison NG, Lincoln SR, Musgrave CB, Miyake GM.

J Polym Sci A Polym Chem. 2017 Sep 15;55(18):3017-3027. doi: 10.1002/pola.28574. Epub 2017 Mar 16.

33.

FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome.

Sherman SL, Kidd SA, Riley C, Berry-Kravis E, Andrews HF, Miller RM, Lincoln S, Swanson M, Kaufmann WE, Brown WT.

Pediatrics. 2017 Jun;139(Suppl 3):S183-S193. doi: 10.1542/peds.2016-1159E.

34.

Suicidal behaviors and their relationship with psychotic-like symptoms in children and adolescents at clinical high risk for psychosis.

D'Angelo EJ, Lincoln SH, Morelli N, Graber K, Tembulkar S, Gonzalez-Heydrich J.

Compr Psychiatry. 2017 Oct;78:31-37. doi: 10.1016/j.comppsych.2017.07.008. Epub 2017 Jul 20.

PMID:
28803039
35.

Consistency of BRCA1 and BRCA2 Variant Classifications Among Clinical Diagnostic Laboratories.

Lincoln SE, Yang S, Cline MS, Kobayashi Y, Zhang C, Topper S, Haussler D, Paten B, Nussbaum RL.

JCO Precis Oncol. 2017 Jul;1. doi: 10.1200/PO.16.00020. Epub 2017 Apr 11.

36.

Outcome of Expedited Rotator Cuff Surgery in Injured Workers: Determinants of Successful Recovery.

Razmjou H, Boljanovic D, Lincoln S, Holtby R, Gallay S, Henry P, Macritchie I; WCP Consortium, Borthwick C, Mayer L, Roknic C, Shore D, Kamino A, Grossman J, Hill J, Singh G, Travers N, Yanofsky L, Wilson M, Sumar S, Savona A, De Medeiros F, Mann H, Champsi A, Chau S, Medeiros D, Richards RR.

Orthop J Sports Med. 2017 May 22;5(5):2325967117705319. doi: 10.1177/2325967117705319. eCollection 2017 May.

37.

Sources of discordance among germ-line variant classifications in ClinVar.

Yang S, Lincoln SE, Kobayashi Y, Nykamp K, Nussbaum RL, Topper S.

Genet Med. 2017 Oct;19(10):1118-1126. doi: 10.1038/gim.2017.60. Epub 2017 Jun 1. Erratum in: Genet Med. 2017 Dec 07;:.

38.

Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype.

Zou F, McWalter K, Schmidt L, Decker A, Picker JD, Lincoln S, Sweetser DA, Briere LC, Harini C; Members of the Undiagnosed Diseases Network, Marsh E, Medne L, Wang RY, Leydiker K, Mower A, Visser G, Cuppen I, van Gassen KL, van der Smagt J, Yousaf A, Tennison M, Shanmugham A, Butler E, Richard G, McKnight D.

J Neurogenet. 2017 Mar - Jun;31(1-2):30-36. doi: 10.1080/01677063.2017.1315417. Epub 2017 May 2.

39.

Social cognitive impairment in 22q11 deletion syndrome: A review.

Norkett EM, Lincoln SH, Gonzalez-Heydrich J, D'Angelo EJ.

Psychiatry Res. 2017 Jul;253:99-106. doi: 10.1016/j.psychres.2017.01.103. Epub 2017 Feb 23. Review.

PMID:
28364592
40.

Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation.

Kobayashi Y, Yang S, Nykamp K, Garcia J, Lincoln SE, Topper SE.

Genome Med. 2017 Feb 6;9(1):13. doi: 10.1186/s13073-017-0403-7.

41.

Clinical Genetics Testing Laboratories Have a Remarkably Low Rate of Clinically Significant Discordance When Interpreting Variants in Hereditary Cancer Syndrome Genes.

Nussbaum RL, Yang S, Lincoln SE.

J Clin Oncol. 2017 Apr 10;35(11):1259-1261. doi: 10.1200/JCO.2016.70.9451. Epub 2017 Jan 30. No abstract available.

PMID:
28135136
42.

The effect of expedited rotator cuff surgery in injured workers: a case-control study.

Razmjou H, Lincoln S, Boljanovic D, Gallay S, Henry P, Richards RR, Holtby R.

J Shoulder Elbow Surg. 2017 Jul;26(7):1196-1202. doi: 10.1016/j.jse.2016.11.049. Epub 2017 Jan 25.

PMID:
28131686
43.

ABCA7 loss-of-function variants, expression, and neurologic disease risk.

Allen M, Lincoln SJ, Corda M, Watzlawik JO, Carrasquillo MM, Reddy JS, Burgess JD, Nguyen T, Malphrus K, Petersen RC, Graff-Radford NR, Dickson DW, Ertekin-Taner N.

Neurol Genet. 2017 Jan 5;3(1):e126. doi: 10.1212/NXG.0000000000000126. eCollection 2017 Feb.

44.

A Developmental Perspective on Social-Cognition Difficulties in Youth at Clinical High Risk for Psychosis.

Lincoln SH, Norkett EM, Frost KH, Gonzalez-Heydrich J, D'Angelo EJ.

Harv Rev Psychiatry. 2017 Jan/Feb;25(1):4-14. doi: 10.1097/HRP.0000000000000125. Review.

PMID:
28059932
45.

A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression.

Carrasquillo MM, Allen M, Burgess JD, Wang X, Strickland SL, Aryal S, Siuda J, Kachadoorian ML, Medway C, Younkin CS, Nair A, Wang C, Chanana P, Serie D, Nguyen T, Lincoln S, Malphrus KG, Morgan K, Golde TE, Price ND, White CC, De Jager PL, Bennett DA, Asmann YW, Crook JE, Petersen RC, Graff-Radford NR, Dickson DW, Younkin SG, Ertekin-Taner N.

Alzheimers Dement. 2017 Jun;13(6):663-673. doi: 10.1016/j.jalz.2016.10.005. Epub 2016 Dec 8.

46.

Management of Acute Work-Related Shoulder Injuries by an Early Shoulder Assessment Program: Efficiency of Imaging Investigations.

Razmjou H, Lincoln S, Geddes C, Boljanovic D, Macritchie I, Virdo-Cristello C, Medeiros D, Richards RR.

Physiother Can. 2016;68(4):357-366.

47.

DATA SHARING AND REPRODUCIBLE CLINICAL GENETIC TESTING: SUCCESSES AND CHALLENGES.

Yang S, Cline M, Zhang C, Paten B, Lincoln SE.

Pac Symp Biocomput. 2017;22:166-176. doi: 10.1142/9789813207813_0017.

48.

Prognostic dilemmas and genetic counseling for prenatally detected fragile X gene expansions.

Finucane B, Lincoln S, Bailey L, Martin CL.

Prenat Diagn. 2017 Jan;37(1):37-42. doi: 10.1002/pd.4963. Epub 2016 Nov 29.

PMID:
27862088
49.

Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases.

Allen M, Carrasquillo MM, Funk C, Heavner BD, Zou F, Younkin CS, Burgess JD, Chai HS, Crook J, Eddy JA, Li H, Logsdon B, Peters MA, Dang KK, Wang X, Serie D, Wang C, Nguyen T, Lincoln S, Malphrus K, Bisceglio G, Li M, Golde TE, Mangravite LM, Asmann Y, Price ND, Petersen RC, Graff-Radford NR, Dickson DW, Younkin SG, Ertekin-Taner N.

Sci Data. 2016 Oct 11;3:160089. doi: 10.1038/sdata.2016.89.

50.

Excited-state dynamics of the medicinal pigment curcumin in a hydrogel.

Harada T, Lincoln SF, Kee TW.

Phys Chem Chem Phys. 2016 Oct 12;18(40):28125-28133.

PMID:
27711741

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