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Items: 1 to 50 of 241

1.

De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.

Mirzaa GM, Chong JX, Piton A, Popp B, Foss K, Guo H, Harripaul R, Xia K, Scheck J, Aldinger KA, Sajan SA, Tang S, Bonneau D, Beck A, White J, Mahida S, Harris J, Smith-Hicks C, Hoyer J, Zweier C, Reis A, Thiel CT, Jamra RA, Zeid N, Yang A, Farach LS, Walsh L, Payne K, Rohena L, Velinov M, Ziegler A, Schaefer E, Gatinois V, Geneviève D, Simon MEH, Kohler J, Rotenberg J, Wheeler P, Larson A, Ernst ME, Akman CI, Westman R, Blanchet P, Schillaci LA, Vincent-Delorme C, Gripp KW, Mattioli F, Guyader GL, Gerard B, Mathieu-Dramard M, Morin G, Sasanfar R, Ayub M, Vasli N, Yang S, Person R, Monaghan KG, Nickerson DA, van Binsbergen E, Enns GM, Dries AM, Rowe LJ, Tsai ACH, Svihovec S, Friedman J, Agha Z, Qamar R, Rodan LH, Martinez-Agosto J, Ockeloen CW, Vincent M, Sunderland WJ, Bernstein JA; Undiagnosed Diseases Network,, Eichler EE, Vincent JB; University of Washington Center for Mendelian Genomics (UW-CMG),, Bamshad MJ.

Genet Med. 2019 Nov 14. doi: 10.1038/s41436-019-0693-9. [Epub ahead of print]

PMID:
31723249
2.

Release of trivalent chromium from serum transferrin is sufficiently rapid to be physiologically relevant.

Edwards KC, Kim H, Vincent JB.

J Inorg Biochem. 2020 Jan;202:110901. doi: 10.1016/j.jinorgbio.2019.110901. Epub 2019 Oct 20.

PMID:
31669693
3.

MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2.

Martínez de Paz A, Khajavi L, Martin H, Claveria-Gimeno R, Tom Dieck S, Cheema MS, Sanchez-Mut JV, Moksa MM, Carles A, Brodie NI, Sheikh TI, Freeman ME, Petrotchenko EV, Borchers CH, Schuman EM, Zytnicki M, Velazquez-Campoy A, Abian O, Hirst M, Esteller M, Vincent JB, Malnou CE, Ausió J.

Epigenetics Chromatin. 2019 Oct 10;12(1):63. doi: 10.1186/s13072-019-0298-1.

4.

Effects of chromium supplementation on body composition, human and animal health, and insulin and glucose metabolism.

Vincent JB.

Curr Opin Clin Nutr Metab Care. 2019 Nov;22(6):483-489. doi: 10.1097/MCO.0000000000000604.

PMID:
31577642
5.

Molecular Structure of Binary Chromium(III)-DNA Adducts.

Brown S, Lockart MM, Thomas CS, Bowman MK, Woski SA, Vincent JB.

Chembiochem. 2019 Aug 31. doi: 10.1002/cbic.201900436. [Epub ahead of print]

PMID:
31472032
6.

GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates.

Ouyang Q, Kavanaugh BC, Joesch-Cohen L, Dubois B, Wu Q, Schmidt M, Baytas O, Pastore SF, Harripaul R, Mishra S, Hussain A, Kim KH, Holler-Managan YF, Ayub M, Mir A, Vincent JB, Liu JS, Morrow EM.

Hum Genet. 2019 Oct;138(10):1183-1200. doi: 10.1007/s00439-019-02057-x. Epub 2019 Aug 30.

PMID:
31471722
7.

Images from the surface of asteroid Ryugu show rocks similar to carbonaceous chondrite meteorites.

Jaumann R, Schmitz N, Ho TM, Schröder SE, Otto KA, Stephan K, Elgner S, Krohn K, Preusker F, Scholten F, Biele J, Ulamec S, Krause C, Sugita S, Matz KD, Roatsch T, Parekh R, Mottola S, Grott M, Michel P, Trauthan F, Koncz A, Michaelis H, Lange C, Grundmann JT, Maibaum M, Sasaki K, Wolff F, Reill J, Moussi-Soffys A, Lorda L, Neumann W, Vincent JB, Wagner R, Bibring JP, Kameda S, Yano H, Watanabe S, Yoshikawa M, Tsuda Y, Okada T, Yoshimitsu T, Mimasu Y, Saiki T, Yabuta H, Rauer H, Honda R, Morota T, Yokota Y, Kouyama T.

Science. 2019 Aug 23;365(6455):817-820. doi: 10.1126/science.aaw8627.

PMID:
31439797
8.

Association of smoked cannabis with treatment resistance in schizophrenia.

Arsalan A, Iqbal Z, Tariq M, Ayonrinde O, Vincent JB, Ayub M.

Psychiatry Res. 2019 Aug;278:242-247. doi: 10.1016/j.psychres.2019.06.023. Epub 2019 Jun 18.

PMID:
31229838
9.

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

Mullins N, Bigdeli TB, Børglum AD, Coleman JRI, Demontis D, Mehta D, Power RA, Ripke S, Stahl EA, Starnawska A, Anjorin A; M.R.C.Psych, Corvin A, Sanders AR, Forstner AJ, Reif A, Koller AC, Świątkowska B, Baune BT, Müller-Myhsok B, Penninx BWJH, Pato C, Zai C, Rujescu D, Hougaard DM, Quested D, Levinson DF, Binder EB, Byrne EM, Agerbo E; Dr.Med.Sc, Streit F, Mayoral F, Bellivier F, Degenhardt F, Breen G, Morken G, Turecki G, Rouleau GA, Grabe HJ, Völzke H, Jones I, Giegling I, Agartz I, Melle I, Lawrence J; M.R.C.Psych, Walters JTR, Strohmaier J, Shi J, Hauser J, Biernacka JM, Vincent JB, Kelsoe J, Strauss JS, Lissowska J, Pimm J; M.R.C.Psych, Smoller JW, Guzman-Parra J, Berger K, Scott LJ, Jones LA, Azevedo MH, Trzaskowski M, Kogevinas M, Rietschel M, Boks M, Ising M, Grigoroiu-Serbanescu M, Hamshere ML, Leboyer M, Frye M, Nöthen MM, Alda M, Preisig M, Nordentoft M, Boehnke M, O'Donovan MC, Owen MJ, Pato MT, Renteria ME, Budde M; Dipl.-Psych, Weissman MM, Wray NR, Bass N; M.R.C.Psych, Craddock N, Smeland OB, Andreassen OA, Mors O, Gejman PV, Sklar P, McGrath P, Hoffmann P, McGuffin P, Lee PH, Mortensen PB, Kahn RS, Ophoff RA, Adolfsson R, Van der Auwera S, Djurovic S, Kloiber S, Heilmann-Heimbach S, Jamain S, Hamilton SP, McElroy SL, Lucae S, Cichon S, Schulze TG, Hansen T, Werge T, Air TM, Nimgaonkar V, Appadurai V, Cahn W, Milaneschi Y; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Fanous AH, Kendler KS, McQuillin A, Lewis CM.

Am J Psychiatry. 2019 Aug 1;176(8):651-660. doi: 10.1176/appi.ajp.2019.18080957. Epub 2019 Jun 5.

PMID:
31164008
10.

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, Pers TH, Holmans PA, Richards AL, Abbott L, Agerbo E, Akil H, Albani D, Alliey-Rodriguez N, Als TD, Anjorin A, Antilla V, Awasthi S, Badner JA, Bækvad-Hansen M, Barchas JD, Bass N, Bauer M, Belliveau R, Bergen SE, Pedersen CB, Bøen E, Boks MP, Boocock J, Budde M, Bunney W, Burmeister M, Bybjerg-Grauholm J, Byerley W, Casas M, Cerrato F, Cervantes P, Chambert K, Charney AW, Chen D, Churchhouse C, Clarke TK, Coryell W, Craig DW, Cruceanu C, Curtis D, Czerski PM, Dale AM, de Jong S, Degenhardt F, Del-Favero J, DePaulo JR, Djurovic S, Dobbyn AL, Dumont A, Elvsåshagen T, Escott-Price V, Fan CC, Fischer SB, Flickinger M, Foroud TM, Forty L, Frank J, Fraser C, Freimer NB, Frisén L, Gade K, Gage D, Garnham J, Giambartolomei C, Pedersen MG, Goldstein J, Gordon SD, Gordon-Smith K, Green EK, Green MJ, Greenwood TA, Grove J, Guan W, Guzman-Parra J, Hamshere ML, Hautzinger M, Heilbronner U, Herms S, Hipolito M, Hoffmann P, Holland D, Huckins L, Jamain S, Johnson JS, Juréus A, Kandaswamy R, Karlsson R, Kennedy JL, Kittel-Schneider S, Knowles JA, Kogevinas M, Koller AC, Kupka R, Lavebratt C, Lawrence J, Lawson WB, Leber M, Lee PH, Levy SE, Li JZ, Liu C, Lucae S, Maaser A, MacIntyre DJ, Mahon PB, Maier W, Martinsson L, McCarroll S, McGuffin P, McInnis MG, McKay JD, Medeiros H, Medland SE, Meng F, Milani L, Montgomery GW, Morris DW, Mühleisen TW, Mullins N, Nguyen H, Nievergelt CM, Adolfsson AN, Nwulia EA, O'Donovan C, Loohuis LMO, Ori APS, Oruc L, Ösby U, Perlis RH, Perry A, Pfennig A, Potash JB, Purcell SM, Regeer EJ, Reif A, Reinbold CS, Rice JP, Rivas F, Rivera M, Roussos P, Ruderfer DM, Ryu E, Sánchez-Mora C, Schatzberg AF, Scheftner WA, Schork NJ, Shannon Weickert C, Shehktman T, Shilling PD, Sigurdsson E, Slaney C, Smeland OB, Sobell JL, Søholm Hansen C, Spijker AT, St Clair D, Steffens M, Strauss JS, Streit F, Strohmaier J, Szelinger S, Thompson RC, Thorgeirsson TE, Treutlein J, Vedder H, Wang W, Watson SJ, Weickert TW, Witt SH, Xi S, Xu W, Young AH, Zandi P, Zhang P, Zöllner S; eQTLGen Consortium; BIOS Consortium, Adolfsson R, Agartz I, Alda M, Backlund L, Baune BT, Bellivier F, Berrettini WH, Biernacka JM, Blackwood DHR, Boehnke M, Børglum AD, Corvin A, Craddock N, Daly MJ, Dannlowski U, Esko T, Etain B, Frye M, Fullerton JM, Gershon ES, Gill M, Goes F, Grigoroiu-Serbanescu M, Hauser J, Hougaard DM, Hultman CM, Jones I, Jones LA, Kahn RS, Kirov G, Landén M, Leboyer M, Lewis CM, Li QS, Lissowska J, Martin NG, Mayoral F, McElroy SL, McIntosh AM, McMahon FJ, Melle I, Metspalu A, Mitchell PB, Morken G, Mors O, Mortensen PB, Müller-Myhsok B, Myers RM, Neale BM, Nimgaonkar V, Nordentoft M, Nöthen MM, O'Donovan MC, Oedegaard KJ, Owen MJ, Paciga SA, Pato C, Pato MT, Posthuma D, Ramos-Quiroga JA, Ribasés M, Rietschel M, Rouleau GA, Schalling M, Schofield PR, Schulze TG, Serretti A, Smoller JW, Stefansson H, Stefansson K, Stordal E, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Werge T, Nurnberger JI, Wray NR, Di Florio A, Edenberg HJ, Cichon S, Ophoff RA, Scott LJ, Andreassen OA, Kelsoe J, Sklar P; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium.

Nat Genet. 2019 May;51(5):793-803. doi: 10.1038/s41588-019-0397-8. Epub 2019 May 1.

PMID:
31043756
11.

Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations.

Gul H, Shah AH, Harripaul R, Mikhailov A, Prajapati K, Khan E, Ullah F, Zubair M, Ali MZ, Shah AH, Salman S, Khan S, Vincent JB, Khan MA.

Ann Hum Genet. 2019 Jul;83(4):278-284. doi: 10.1111/ahg.12307. Epub 2019 Mar 13.

PMID:
30868578
12.

Bears habituate to the repeated exposure of a novel stimulus, unmanned aircraft systems.

Ditmer MA, Werden LK, Tanner JC, Vincent JB, Callahan P, Iaizzo PA, Laske TG, Garshelis DL.

Conserv Physiol. 2019 Jan 14;7(1):coy067. doi: 10.1093/conphys/coy067. eCollection 2019.

13.

Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populations.

Sriretnakumar V, Harripaul R, Vincent JB, Kennedy JL, So J.

Am J Med Genet B Neuropsychiatr Genet. 2019 Jan;180(1):46-54. doi: 10.1002/ajmg.b.32702. Epub 2018 Dec 16.

PMID:
30556376
14.

Systematic Review of the Effects of Chromium(III) on Chickens.

White PE, Vincent JB.

Biol Trace Elem Res. 2019 Mar;188(1):99-126. doi: 10.1007/s12011-018-1575-8. Epub 2018 Nov 14.

PMID:
30430417
15.

The use of chromium(III) complexes to enhance peptide protonation by electrospray ionization mass spectrometry.

Jing X, Edwards KC, Vincent JB, Cassady CJ.

J Mass Spectrom. 2018 Dec;53(12):1198-1206. doi: 10.1002/jms.4297.

PMID:
30281192
16.

Chromium.

Vincent JB, Lukaski HC.

Adv Nutr. 2018 Jul 1;9(4):505-506. doi: 10.1093/advances/nmx021.

17.

Sequence Analysis of Drug Target Genes with Suicidal Behavior in Bipolar Disorder Patients.

Zai CC, Tiwari AK, Zai GC, de Luca V, Shaikh SA, King N, Strauss J, Kennedy JL, Vincent JB.

Mol Neuropsychiatry. 2018 Jun;4(1):1-6. doi: 10.1159/000488029. Epub 2018 May 3.

18.

Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.

Fattahi Z, Sheikh TI, Musante L, Rasheed M, Taskiran II, Harripaul R, Hu H, Kazeminasab S, Alam MR, Hosseini M, Larti F, Ghaderi Z, Celik A, Ayub M, Ansar M, Haddadi M, Wienker TF, Ropers HH, Kahrizi K, Vincent JB, Najmabadi H.

Hum Mol Genet. 2018 Sep 15;27(18):3177-3188. doi: 10.1093/hmg/ddy220.

PMID:
29893856
19.

Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene GPR56 in Pakistani Intellectual Disability Families.

Sawal HA, Harripaul R, Mikhailov A, Vleuten K, Naeem F, Nasr T, Hassan MJ, Vincent JB, Ayub M, Rafiq MA.

J Pediatr Genet. 2018 Jun;7(2):60-66. doi: 10.1055/s-0037-1612591. Epub 2017 Dec 21.

20.

MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro.

Sheikh TI, Harripaul R, Ayub M, Vincent JB.

Hum Mutat. 2018 May;39(5):717-728. doi: 10.1002/humu.23409. Epub 2018 Mar 8.

PMID:
29431277
21.

New Evidence against Chromium as an Essential Trace Element.

Vincent JB.

J Nutr. 2017 Dec;147(12):2212-2219. doi: 10.3945/jn.117.255901. Epub 2017 Oct 11. Review.

PMID:
29021369
22.

MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.

Sheikh TI, de Paz AM, Akhtar S, Ausió J, Vincent JB.

Hum Mol Genet. 2017 Nov 1;26(21):4132-4141. doi: 10.1093/hmg/ddx300.

23.

[Cr3O(O2CCH2CH3)6(H2O)3]NO3·H2O (Cr3) Toxicity Potential in Bacterial and Mammalian Cells.

Jiang L, Vincent JB, Bailey MM.

Biol Trace Elem Res. 2018 Jun;183(2):342-350. doi: 10.1007/s12011-017-1132-x. Epub 2017 Sep 7.

PMID:
28879636
24.

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Witt SH, Streit F, Jungkunz M, Frank J, Awasthi S, Reinbold CS, Treutlein J, Degenhardt F, Forstner AJ, Heilmann-Heimbach S, Dietl L, Schwarze CE, Schendel D, Strohmaier J, Abdellaoui A, Adolfsson R, Air TM, Akil H, Alda M, Alliey-Rodriguez N, Andreassen OA, Babadjanova G, Bass NJ, Bauer M, Baune BT, Bellivier F, Bergen S, Bethell A, Biernacka JM, Blackwood DHR, Boks MP, Boomsma DI, Børglum AD, Borrmann-Hassenbach M, Brennan P, Budde M, Buttenschøn HN, Byrne EM, Cervantes P, Clarke TK, Craddock N, Cruceanu C, Curtis D, Czerski PM, Dannlowski U, Davis T, de Geus EJC, Di Florio A, Djurovic S, Domenici E, Edenberg HJ, Etain B, Fischer SB, Forty L, Fraser C, Frye MA, Fullerton JM, Gade K, Gershon ES, Giegling I, Gordon SD, Gordon-Smith K, Grabe HJ, Green EK, Greenwood TA, Grigoroiu-Serbanescu M, Guzman-Parra J, Hall LS, Hamshere M, Hauser J, Hautzinger M, Heilbronner U, Herms S, Hitturlingappa S, Hoffmann P, Holmans P, Hottenga JJ, Jamain S, Jones I, Jones LA, Juréus A, Kahn RS, Kammerer-Ciernioch J, Kirov G, Kittel-Schneider S, Kloiber S, Knott SV, Kogevinas M, Landén M, Leber M, Leboyer M, Li QS, Lissowska J, Lucae S, Martin NG, Mayoral-Cleries F, McElroy SL, McIntosh AM, McKay JD, McQuillin A, Medland SE, Middeldorp CM, Milaneschi Y, Mitchell PB, Montgomery GW, Morken G, Mors O, Mühleisen TW, Müller-Myhsok B, Myers RM, Nievergelt CM, Nurnberger JI, O'Donovan MC, Loohuis LMO, Ophoff R, Oruc L, Owen MJ, Paciga SA, Penninx BWJH, Perry A, Pfennig A, Potash JB, Preisig M, Reif A, Rivas F, Rouleau GA, Schofield PR, Schulze TG, Schwarz M, Scott L, Sinnamon GCB, Stahl EA, Strauss J, Turecki G, Van der Auwera S, Vedder H, Vincent JB, Willemsen G, Witt CC, Wray NR, Xi HS; Bipolar Disorders Working Group of the Psychiatric Genomics Consortium; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Tadic A, Dahmen N, Schott BH, Cichon S, Nöthen MM, Ripke S, Mobascher A, Rujescu D, Lieb K, Roepke S, Schmahl C, Bohus M, Rietschel M.

Transl Psychiatry. 2017 Jun 20;7(6):e1155. doi: 10.1038/tp.2017.115.

25.

The Identity of "Chromium Malate".

Smart M, Brown S, Tannehill H, Lockart M, Bowman MK, Vincent JB.

Biol Trace Elem Res. 2018 Feb;181(2):369-377. doi: 10.1007/s12011-017-1046-7. Epub 2017 May 18.

PMID:
28516390
26.

Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse.

Ung DC, Iacono G, Méziane H, Blanchard E, Papon MA, Selten M, van Rhijn JR, Montjean R, Rucci J, Martin S, Fleet A, Birling MC, Marouillat S, Roepman R, Selloum M, Lux A, Thépault RA, Hamel P, Mittal K, Vincent JB, Dorseuil O, Stunnenberg HG, Billuart P, Nadif Kasri N, Hérault Y, Laumonnier F.

Mol Psychiatry. 2018 May;23(5):1356-1367. doi: 10.1038/mp.2017.39. Epub 2017 Apr 18.

27.

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.

Harripaul R, Vasli N, Mikhailov A, Rafiq MA, Mittal K, Windpassinger C, Sheikh TI, Noor A, Mahmood H, Downey S, Johnson M, Vleuten K, Bell L, Ilyas M, Khan FS, Khan V, Moradi M, Ayaz M, Naeem F, Heidari A, Ahmed I, Ghadami S, Agha Z, Zeinali S, Qamar R, Mozhdehipanah H, John P, Mir A, Ansar M, French L, Ayub M, Vincent JB.

Mol Psychiatry. 2018 Apr;23(4):973-984. doi: 10.1038/mp.2017.60. Epub 2017 Apr 11.

PMID:
28397838
28.

Surface changes on comet 67P/Churyumov-Gerasimenko suggest a more active past.

El-Maarry MR, Groussin O, Thomas N, Pajola M, Auger AT, Davidsson B, Hu X, Hviid SF, Knollenberg J, Güttler C, Tubiana C, Fornasier S, Feller C, Hasselmann P, Vincent JB, Sierks H, Barbieri C, Lamy P, Rodrigo R, Koschny D, Keller HU, Rickman H, A'Hearn MF, Barucci MA, Bertaux JL, Bertini I, Besse S, Bodewits D, Cremonese G, Da Deppo V, Debei S, De Cecco M, Deller J, Deshapriya JD, Fulle M, Gutierrez PJ, Hofmann M, Ip WH, Jorda L, Kovacs G, Kramm JR, Kührt E, Küppers M, Lara LM, Lazzarin M, Lin ZY, Lopez Moreno JJ, Marchi S, Marzari F, Mottola S, Naletto G, Oklay N, Pommerol A, Preusker F, Scholten F, Shi X.

Science. 2017 Mar 31;355(6332):1392-1395. doi: 10.1126/science.aak9384. Epub 2017 Mar 21.

PMID:
28325842
29.

Investigation of correlations between DNA methylation, suicidal behavior and aging.

Jeremian R, Chen YA, De Luca V, Vincent JB, Kennedy JL, Zai CC, Strauss J.

Bipolar Disord. 2017 Feb;19(1):32-40. doi: 10.1111/bdi.12466. Epub 2017 Mar 9.

PMID:
28276657
30.

The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual Disability.

Harripaul R, Noor A, Ayub M, Vincent JB.

Cold Spring Harb Perspect Med. 2017 Mar 1;7(3). pii: a026864. doi: 10.1101/cshperspect.a026864. Review.

31.

Summaries of plenary and selected symposia sessions at the XXIV World Congress of Psychiatric Genetics; Jerusalem, Israel; 30 October 2016-3 November 2016.

Ciobanu LG, Ori AP, Pagliaroli L, Polimanti R, Spindola LM, Vincent JB, Cormack FK.

Psychiatr Genet. 2017 Apr;27(2):41-53. doi: 10.1097/YPG.0000000000000167.

PMID:
28212207
32.

Relative importance of abiotic, biotic, and disturbance drivers of plant community structure in the sagebrush steppe.

Mitchell RM, Bakker JD, Vincent JB, Davies GM.

Ecol Appl. 2017 Apr;27(3):756-768. doi: 10.1002/eap.1479. Epub 2017 Mar 15.

PMID:
27935663
33.

From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.

Sheikh TI, Ausió J, Faghfoury H, Silver J, Lane JB, Eubanks JH, MacLeod P, Percy AK, Vincent JB.

Sci Rep. 2016 Dec 8;6:38590. doi: 10.1038/srep38590.

34.

Rosetta's comet 67P/Churyumov-Gerasimenko sheds its dusty mantle to reveal its icy nature.

Fornasier S, Mottola S, Keller HU, Barucci MA, Davidsson B, Feller C, Deshapriya JD, Sierks H, Barbieri C, Lamy PL, Rodrigo R, Koschny D, Rickman H, A'Hearn M, Agarwal J, Bertaux JL, Bertini I, Besse S, Cremonese G, Da Deppo V, Debei S, De Cecco M, Deller J, El-Maarry MR, Fulle M, Groussin O, Gutierrez PJ, Güttler C, Hofmann M, Hviid SF, Ip WH, Jorda L, Knollenberg J, Kovacs G, Kramm R, Kührt E, Küppers M, Lara ML, Lazzarin M, Moreno JJ, Marzari F, Massironi M, Naletto G, Oklay N, Pajola M, Pommerol A, Preusker F, Scholten F, Shi X, Thomas N, Toth I, Tubiana C, Vincent JB.

Science. 2016 Dec 23;354(6319):1566-1570. doi: 10.1126/science.aag2671. Epub 2016 Nov 17.

PMID:
27856849
35.

Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability.

Mittal K, Rafiq MA, Rafiullah R, Harripaul R, Ali H, Ayaz M, Aslam M, Naeem F, Amin-Ud-Din M, Waqas A, So J, Rappold GA, Vincent JB, Ayub M.

J Hum Genet. 2016 Oct;61(10):867-872. doi: 10.1038/jhg.2016.62. Epub 2016 Jun 16.

PMID:
27305979
36.

Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan.

Sawal HA, Harripaul R, Mikhailov A, Dad R, Ayub M, Jawad Hassan M, Vincent JB.

Clin Genet. 2016 Dec;90(6):563-565. doi: 10.1111/cge.12860. Epub 2016 Oct 17.

PMID:
27747863
37.

Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features.

Johansen A, Rosti RO, Musaev D, Sticca E, Harripaul R, Zaki M, Çağlayan AO, Azam M, Sultan T, Froukh T, Reis A, Popp B, Ahmed I, John P, Ayub M, Ben-Omran T, Vincent JB, Gleeson JG, Abou Jamra R.

Am J Hum Genet. 2016 Oct 6;99(4):912-916. doi: 10.1016/j.ajhg.2016.07.019. Epub 2016 Sep 8.

38.

The effects of the glycation of transferrin on chromium binding and the transport and distribution of chromium in vivo.

Deng G, Dyroff SL, Lockart M, Bowman MK, Vincent JB.

J Inorg Biochem. 2016 Nov;164:26-33. doi: 10.1016/j.jinorgbio.2016.08.008. Epub 2016 Aug 25.

PMID:
27592288
39.

A reference panel of 64,976 haplotypes for genotype imputation.

McCarthy S, Das S, Kretzschmar W, Delaneau O, Wood AR, Teumer A, Kang HM, Fuchsberger C, Danecek P, Sharp K, Luo Y, Sidore C, Kwong A, Timpson N, Koskinen S, Vrieze S, Scott LJ, Zhang H, Mahajan A, Veldink J, Peters U, Pato C, van Duijn CM, Gillies CE, Gandin I, Mezzavilla M, Gilly A, Cocca M, Traglia M, Angius A, Barrett JC, Boomsma D, Branham K, Breen G, Brummett CM, Busonero F, Campbell H, Chan A, Chen S, Chew E, Collins FS, Corbin LJ, Smith GD, Dedoussis G, Dorr M, Farmaki AE, Ferrucci L, Forer L, Fraser RM, Gabriel S, Levy S, Groop L, Harrison T, Hattersley A, Holmen OL, Hveem K, Kretzler M, Lee JC, McGue M, Meitinger T, Melzer D, Min JL, Mohlke KL, Vincent JB, Nauck M, Nickerson D, Palotie A, Pato M, Pirastu N, McInnis M, Richards JB, Sala C, Salomaa V, Schlessinger D, Schoenherr S, Slagboom PE, Small K, Spector T, Stambolian D, Tuke M, Tuomilehto J, Van den Berg LH, Van Rheenen W, Volker U, Wijmenga C, Toniolo D, Zeggini E, Gasparini P, Sampson MG, Wilson JF, Frayling T, de Bakker PI, Swertz MA, McCarroll S, Kooperberg C, Dekker A, Altshuler D, Willer C, Iacono W, Ripatti S, Soranzo N, Walter K, Swaroop A, Cucca F, Anderson CA, Myers RM, Boehnke M, McCarthy MI, Durbin R; Haplotype Reference Consortium.

Nat Genet. 2016 Oct;48(10):1279-83. doi: 10.1038/ng.3643. Epub 2016 Aug 22.

40.

Ectomycorrhizal fungal diversity and saprotrophic fungal diversity are linked to different tree community attributes in a field-based tree experiment.

Nguyen NH, Williams LJ, Vincent JB, Stefanski A, Cavender-Bares J, Messier C, Paquette A, Gravel D, Reich PB, Kennedy PG.

Mol Ecol. 2016 Aug;25(16):4032-46. doi: 10.1111/mec.13719. Epub 2016 Jul 29.

PMID:
27284759
41.

Unstable repeat expansion in major psychiatric disorders: two decades on, is dynamic DNA back on the menu?

Vincent JB.

Psychiatr Genet. 2016 Aug;26(4):156-65. doi: 10.1097/YPG.0000000000000141. Review.

PMID:
27270050
42.

Histone Variants and Composition in the Developing Brain: Should MeCP2 Care?

Zago V, Pinar-CabezaDeVaca C, Vincent JB, Ausio J.

Curr Top Med Chem. 2017;17(7):829-842. Review.

PMID:
27086783
43.

Spectroscopic and biological activity studies of the chromium-binding peptide EEEEGDD.

Arakawa H, Kandadi MR, Panzhinskiy E, Belmore K, Deng G, Love E, Robertson PM, Commodore JJ, Cassady CJ, Nair S, Vincent JB.

J Biol Inorg Chem. 2016 Jun;21(3):369-81. doi: 10.1007/s00775-016-1347-x. Epub 2016 Feb 22.

PMID:
26898644
44.

Host associations and beta diversity of fungal endophyte communities in New Guinea rainforest trees.

Vincent JB, Weiblen GD, May G.

Mol Ecol. 2016 Feb;25(3):825-41. doi: 10.1111/mec.13510. Epub 2016 Jan 19.

PMID:
26661903
45.

Sublimation in bright spots on (1) Ceres.

Nathues A, Hoffmann M, Schaefer M, Le Corre L, Reddy V, Platz T, Cloutis EA, Christensen U, Kneissl T, Li JY, Mengel K, Schmedemann N, Schaefer T, Russell CT, Applin DM, Buczkowski DL, Izawa MR, Keller HU, O'Brien DP, Pieters CM, Raymond CA, Ripken J, Schenk PM, Schmidt BE, Sierks H, Sykes MV, Thangjam GS, Vincent JB.

Nature. 2015 Dec 10;528(7581):237-40. doi: 10.1038/nature15754.

PMID:
26659183
46.

Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability.

Vasli N, Ahmed I, Mittal K, Ohadi M, Mikhailov A, Rafiq MA, Bhatti A, Carter MT, Andrade DM, Ayub M, Vincent JB, John P.

Psychiatr Genet. 2016 Apr;26(2):66-73. doi: 10.1097/YPG.0000000000000114.

PMID:
26529358
47.

Two independent and primitive envelopes of the bilobate nucleus of comet 67P.

Massironi M, Simioni E, Marzari F, Cremonese G, Giacomini L, Pajola M, Jorda L, Naletto G, Lowry S, El-Maarry MR, Preusker F, Scholten F, Sierks H, Barbieri C, Lamy P, Rodrigo R, Koschny D, Rickman H, Keller HU, A'Hearn MF, Agarwal J, Auger AT, Barucci MA, Bertaux JL, Bertini I, Besse S, Bodewits D, Capanna C, Da Deppo V, Davidsson B, Debei S, De Cecco M, Ferri F, Fornasier S, Fulle M, Gaskell R, Groussin O, Gutiérrez PJ, Güttler C, Hviid SF, Ip WH, Knollenberg J, Kovacs G, Kramm R, Kührt E, Küppers M, La Forgia F, Lara LM, Lazzarin M, Lin ZY, Lopez Moreno JJ, Magrin S, Michalik H, Mottola S, Oklay N, Pommerol A, Thomas N, Tubiana C, Vincent JB.

Nature. 2015 Oct 15;526(7573):402-5. doi: 10.1038/nature15511. Epub 2015 Sep 28.

PMID:
26416730
48.

Bears Show a Physiological but Limited Behavioral Response to Unmanned Aerial Vehicles.

Ditmer MA, Vincent JB, Werden LK, Tanner JC, Laske TG, Iaizzo PA, Garshelis DL, Fieberg JR.

Curr Biol. 2015 Aug 31;25(17):2278-83. doi: 10.1016/j.cub.2015.07.024. Epub 2015 Aug 13.

49.

Trophic phylogenetics: evolutionary influences on body size, feeding, and species associations in grassland arthropods.

Lind EM, Vincent JB, Weiblen GD, Cavender-Bares J, Borer ET.

Ecology. 2015 Apr;96(4):998-1009.

PMID:
26230020
50.

Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.

Heidari A, Tongsook C, Najafipour R, Musante L, Vasli N, Garshasbi M, Hu H, Mittal K, McNaughton AJ, Sritharan K, Hudson M, Stehr H, Talebi S, Moradi M, Darvish H, Arshad Rafiq M, Mozhdehipanah H, Rashidinejad A, Samiei S, Ghadami M, Windpassinger C, Gillessen-Kaesbach G, Tzschach A, Ahmed I, Mikhailov A, Stavropoulos DJ, Carter MT, Keshavarz S, Ayub M, Najmabadi H, Liu X, Ropers HH, Macheroux P, Vincent JB.

Hum Mol Genet. 2015 Oct 15;24(20):5697-710. doi: 10.1093/hmg/ddv286. Epub 2015 Jul 23.

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