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Items: 1 to 20 of 34

1.

Drug-resistant epilepsy classified by a phenotyping algorithm associates with NTRK2.

Almoguera B, McGinnis E, Abrams D, Vazquez L, Cederquist A, Sleiman PM, Dlugos D, Hakonarson H; eMERGE Epilepsy Research Group.

Acta Neurol Scand. 2019 May 9. doi: 10.1111/ane.13115. [Epub ahead of print]

PMID:
31070779
2.

Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa.

Chang X, Qu H, Liu Y, Glessner J, Hou C, Wang F, Li J, Sleiman P, Hakonarson H.

J Psychiatr Res. 2019 Jun;113:34-38. doi: 10.1016/j.jpsychires.2019.01.021. Epub 2019 Jan 29.

PMID:
30878790
3.

A sensitive and selective electroanalysis strategy for histidine using the wettable well electrodes modified with graphene quantum dot-scaffolded melamine and copper nanocomposites.

Hua Y, Li S, Cai Y, Liu H, Wan Y, Yin M, Wang F, Wang H.

Nanoscale. 2019 Jan 31;11(5):2126-2130. doi: 10.1039/c8nr08294d.

PMID:
30656322
4.

One-Step Synthesis of FA-Directing FAPbBr3 Perovskite Nanocrystals toward High-Performance Display.

Tong YL, Zhang YW, Ma K, Cheng R, Wang F, Chen S.

ACS Appl Mater Interfaces. 2018 Sep 19;10(37):31603-31609. doi: 10.1021/acsami.8b10366. Epub 2018 Sep 10.

PMID:
30152231
5.

Environmental attitudes in China: The roles of the Dark Triad, future orientation and place attachment.

Huang N, Zuo S, Wang F, Cai P, Wang F.

Int J Psychol. 2018 Jul 24. doi: 10.1002/ijop.12518. [Epub ahead of print]

PMID:
30043481
6.

Reconstructible Nonlinear Dimensionality Reduction via Joint Dictionary Learning.

Wei X, Shen H, Li Y, Tang X, Wang F, Kleinsteuber M, Murphey YL.

IEEE Trans Neural Netw Learn Syst. 2019 Jan;30(1):175-189. doi: 10.1109/TNNLS.2018.2836802. Epub 2018 Jun 5.

PMID:
29994337
7.

Retinoic acid-loaded alginate microspheres as a slow release drug delivery carrier for intravitreal treatment.

Wang F, He S, Chen B.

Biomed Pharmacother. 2018 Jan;97:722-728. doi: 10.1016/j.biopha.2017.10.109. Epub 2017 Nov 6.

PMID:
29102915
8.

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

Li D, Chang X, Connolly JJ, Tian L, Liu Y, Bhoj EJ, Robinson N, Abrams D, Li YR, Bradfield JP, Kim CE, Li J, Wang F, Snyder J, Lemma M, Hou C, Wei Z, Guo Y, Qiu H, Mentch FD, Thomas KA, Chiavacci RM, Cone R, Li B, Sleiman PA; Eating Disorders Working Group of the Psychiatric Genomics Consortium; Price Foundation Collaborative Group, Hakonarson H.

Sci Rep. 2017 Aug 21;7(1):8379. doi: 10.1038/s41598-017-06409-3.

9.

The Dark Side of Malleability: Incremental Theory Promotes Immoral Behaviors.

Huang N, Zuo S, Wang F, Cai P, Wang F.

Front Psychol. 2017 Aug 7;8:1341. doi: 10.3389/fpsyg.2017.01341. eCollection 2017.

10.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

Li D, Chang X, Connolly JJ, Tian L, Liu Y, Bhoj EJ, Robinson N, Abrams D, Li YR, Bradfield JP, Kim CE, Li J, Wang F, Snyder J, Lemma M, Hou C, Wei Z, Guo Y, Qiu H, Mentch FD, Thomas KA, Chiavacci RM, Cone R, Li B, Sleiman PA; Eating Disorders Working Group of the Psychiatric Genomics Consortium; Price Foundation Collaborative Group, Hakonarson H.

Sci Rep. 2017 Jun 19;7(1):3847. doi: 10.1038/s41598-017-01674-8. Erratum in: Sci Rep. 2017 Aug 21;7(1):8379.

11.

A retrospective study of eyeball rupture in patients with or without orbital fracture.

Chen X, Yao Y, Wang F, Liu T, Zhao X.

Medicine (Baltimore). 2017 Jun;96(24):e7109. doi: 10.1097/MD.0000000000007109.

12.

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study.

Cardinale CJ, Li D, Tian L, Connolly JJ, March ME, Hou C, Wang F, Snyder J, Kim CE, Chiavacci RM, Sleiman PM, Burnham JM, Hakonarson H.

BMC Musculoskelet Disord. 2016 Nov 9;17(1):462.

13.

Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain Function.

Li D, Bhoj E, McCormick E, Wang F, Snyder J, Wang T, Zhao Y, Kim C, Chiavacci R, Tian L, Falk MJ, Hakonarson H.

Case Rep Genet. 2016;2016:4140780. doi: 10.1155/2016/4140780. Epub 2016 Mar 16.

14.

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Liu Y, Li Y, March ME, Nguyen K, Xu K, Wang F, Guo Y, Keating B, Glessner J, Li J, Ganley TJ, Zhang J, Deardorff MA, Xu X, Hakonarson H.

Hum Genomics. 2016 Jan 18;10:5. doi: 10.1186/s40246-016-0060-8. No abstract available.

15.

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Liu Y, Li Y, March ME, Nguyen K, Xu K, Wang F, Guo Y, Keating B, Glessner J, Li J, Ganley TJ, Zhang J, Deardorff MA, Xu X, Hakonarson H.

Hum Genomics. 2015 Nov 11;9:31. doi: 10.1186/s40246-015-0053-z. Erratum in: Hum Genomics. 2016;10:5. Kenny, Nguyen [corrected to Nguyen, Kenny].

16.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

Li YR, Zhao SD, Li J, Bradfield JP, Mohebnasab M, Steel L, Kobie J, Abrams DJ, Mentch FD, Glessner JT, Guo Y, Wei Z, Connolly JJ, Cardinale CJ, Bakay M, Li D, Maggadottir SM, Thomas KA, Qui H, Chiavacci RM, Kim CE, Wang F, Snyder J, Flatø B, Førre Ø, Denson LA, Thompson SD, Becker ML, Guthery SL, Latiano A, Perez E, Resnick E, Strisciuglio C, Staiano A, Miele E, Silverberg MS, Lie BA, Punaro M, Russell RK, Wilson DC, Dubinsky MC, Monos DS, Annese V, Munro JE, Wise C, Chapel H, Cunningham-Rundles C, Orange JS, Behrens EM, Sullivan KE, Kugathasan S, Griffiths AM, Satsangi J, Grant SFA, Sleiman PMA, Finkel TH, Polychronakos C, Baldassano RN, Luning Prak ET, Ellis JA, Li H, Keating BJ, Hakonarson H.

Nat Commun. 2015 Oct 9;6:8442. doi: 10.1038/ncomms9442.

17.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.

Li YR, Li J, Zhao SD, Bradfield JP, Mentch FD, Maggadottir SM, Hou C, Abrams DJ, Chang D, Gao F, Guo Y, Wei Z, Connolly JJ, Cardinale CJ, Bakay M, Glessner JT, Li D, Kao C, Thomas KA, Qiu H, Chiavacci RM, Kim CE, Wang F, Snyder J, Richie MD, Flatø B, Førre Ø, Denson LA, Thompson SD, Becker ML, Guthery SL, Latiano A, Perez E, Resnick E, Russell RK, Wilson DC, Silverberg MS, Annese V, Lie BA, Punaro M, Dubinsky MC, Monos DS, Strisciuglio C, Staiano A, Miele E, Kugathasan S, Ellis JA, Munro JE, Sullivan KE, Wise CA, Chapel H, Cunningham-Rundles C, Grant SF, Orange JS, Sleiman PM, Behrens EM, Griffiths AM, Satsangi J, Finkel TH, Keinan A, Prak ET, Polychronakos C, Baldassano RN, Li H, Keating BJ, Hakonarson H.

Nat Med. 2015 Sep;21(9):1018-27. doi: 10.1038/nm.3933. Epub 2015 Aug 24.

18.

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.

Li J, Fung I, Glessner JT, Pandey R, Wei Z, Bakay M, Mentch FD, Pellegrino R, Wang T, Kim C, Hou C, Wang F, Chiavacci RM, Thomas KA, Spergel JM, Hakonarson H, Sleiman PM.

J Immunol. 2015 Aug 15;195(4):1599-607. doi: 10.4049/jimmunol.1402310. Epub 2015 Jul 17.

19.

An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2.

Mancini C, Orsi L, Guo Y, Li J, Chen Y, Wang F, Tian L, Liu X, Zhang J, Jiang H, Nmezi BS, Tatsuta T, Giorgio E, Di Gregorio E, Cavalieri S, Pozzi E, Mortara P, Caglio MM, Balducci A, Pinessi L, Langer T, Padiath QS, Hakonarson H, Zhang X, Brusco A.

BMC Med Genet. 2015 Mar 19;16:16. doi: 10.1186/s12881-015-0159-0.

20.

Rare variants at 16p11.2 are associated with common variable immunodeficiency.

Maggadottir SM, Li J, Glessner JT, Li YR, Wei Z, Chang X, Mentch FD, Thomas KA, Kim CE, Zhao Y, Hou C, Wang F, Jørgensen SF, Perez EE, Sullivan KE, Orange JS, Karlsen TH, Chapel H, Cunningham-Rundles C, Hakonarson H.

J Allergy Clin Immunol. 2015 Jun;135(6):1569-77. doi: 10.1016/j.jaci.2014.12.1939. Epub 2015 Feb 10.

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