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Items: 1 to 50 of 93

1.

Efficient Epileptic Seizure Prediction based on Deep Learning.

Daoud H, Bayoumi M.

IEEE Trans Biomed Circuits Syst. 2019 Jul 17. doi: 10.1109/TBCAS.2019.2929053. [Epub ahead of print]

PMID:
31331897
2.

Infective endocarditis and brain abscess secondary to Aggregatibacter aphrophilus.

Daoud H, Abugroun A, Olanipekun O, Garrison D.

IDCases. 2019 May 17;17:e00561. doi: 10.1016/j.idcr.2019.e00561. eCollection 2019.

3.

Chronic Type A Aortic Dissection: Rare Presentation of Incidental Pericardial Effusion.

Abugroun A, Subahi A, Gaznabi S, Daoud H.

Case Rep Cardiol. 2019 May 2;2019:3562871. doi: 10.1155/2019/3562871. eCollection 2019.

4.

Poster abstracts of the 4th Congress of Tunisian Society of Oncology Radiotherapy (STOR). November 2018.

Kallel A, Khanfir A, Jmal A, Essadok A, Khalfallah A, Boussarsar A, Chamsi A, Yousfi A, Mezlini A, Hdiji A, Moalla A, Mtibaa A, Belaïd A, Ghorbel A, Hadhri A, Hamdoun A, Oualha A, Keskes A, Graja Ben Cheikha B, Daoud B, Hammemi B, Zaidi C, Ben Ammar C, Nasr C, Yazid D, Daoud J, Zaidi E, Dhouib F, Elloumi F, Noubbigh GEF, Jaffel H, Abdelhédi H, Kammoun H, Ouaz H, Bensalah H, Njeh H, Daoud H, Abdelatif I, Chabchoub I, Chaffai I, Werda I, Saidani I, Naceur I, Yahiaoui J, Chaabène K, Khabir A, Ben Zid K, Meddeb K, Ben Fradj K, Mahjoubi K, Meddeb K, Ben Mahfoudh K, Farhat L, Ghorbal L, Mrissa L, Ben Salem L, Kochbati L, Jebsi M, Bohli M, Bouhamed M, Mahdouani M, Fourati M, Morroka K, Ben Rejeb M, Kallel M, Besbes M, Toumi N, Neifar N, Bouzid N, Nsiri N, Tounsi N, Fourati N, Gouiaa N, Absi N, Chaari N, Fourati N, Bouaouina N, Toumi N, Kammoun O, Nouri O, Braikia R, Mzali R, Ben Amor R, Abidi R, Moujahed R, Trigui R, Meftah S, Tbessi S, Boughanmi S, Yahyaoui S, Gritli S, Soltani S, Tebra S, Tebra Mrad S, Kannoun Belajouza S, Kanoun S, Gamra S, Saghaier S, Zaraa S, Zouari S, Kdous S, Haddar S, Ben Dhia S, Sghaier S, Boudawara T, Sahnoun T, Salem Zrafi W, Mnejja W, Ben Kridis W, Gargouri W, Siala W, Abid W, Boudawara Z, Fessi Z.

Tunis Med. 2018 Dec;96(12):911-931. No abstract available.

5.

Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories.

Ghani M, Nfonsam L, Pranckeviciene E, Daoud H, Potter R, Chisholm C, Harper PE, Schaffer A, Little L, Sinclair-Bourque E, McGowan-Jordan J, Smith A, Bronicki L, Jarinova O.

J Mol Diagn. 2019 Jul;21(4):602-611. doi: 10.1016/j.jmoldx.2019.02.009. Epub 2019 Apr 25.

PMID:
31028938
6.

Fixed-target serial oscillation crystallography at room temperature.

Wierman JL, Paré-Labrosse O, Sarracini A, Besaw JE, Cook MJ, Oghbaey S, Daoud H, Mehrabi P, Kriksunov I, Kuo A, Schuller DJ, Smith S, Ernst OP, Szebenyi DME, Gruner SM, Miller RJD, Finke AD.

IUCrJ. 2019 Feb 23;6(Pt 2):305-316. doi: 10.1107/S2052252519001453. eCollection 2019 Mar 1.

7.

Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting.

Daoud H, Ghani M, Nfonsam L, Potter R, Ordorica S, Haslett V, Santos N, Derksen H, Lahey D, McGill M, Trudel V, Antoniuk B, Vasli N, Chisholm C, Mettler G, Sinclair-Bourque E, McGowan-Jordan J, Smith A, Roberts R, Jarinova O.

J Mol Diagn. 2019 May;21(3):437-448. doi: 10.1016/j.jmoldx.2019.01.004. Epub 2019 Feb 4.

PMID:
30731207
8.

[Contribution and limits of intensity-modulated reirradiation of nasopharyngeal carcinomas].

Farhat L, Mnejja W, Fourati N, Daoud H, Sahnoun T, Ben Kridis W, Ghorbel A, Frikha M, Siala W, Daoud J.

Cancer Radiother. 2019 Feb;23(1):28-33. doi: 10.1016/j.canrad.2018.03.010. Epub 2018 Dec 15. French.

PMID:
30563746
9.

Poster abstracts of the 18th Pan Arab Cancer Congress. TUNISIA. April 19-21, 2018.

Aarab J, Abbess I, Abdalla F, Abdelaziz Z, Abdelfattah S, Abdelli I, Abdelmajid K, Abdelsselem Z, Abdelwahed N, Abdessayed N, Abid B, Abid K, Abidi R, Abudabbous A, Abujanah S, Aburwais A, Acacha E, Acharfi N, Affes N, Aftis R, Ahalli I, Aid M, Aissaoui D, Alaoui A, Alaoui M, Albatran S, Mamdouh A, Alkikkli R, Allam A, Aloulou S, Alqawi O, Alragig MA, Alsharksi A, Amaadour KOL, Amaadour L, Ameziane N, Ammari A, Ammour H, Amrane R, Annad N, Aouati E, Aouichat S, Aouragh S, Arifi S, Astra M, Atassi M, Ati N, Atoui K, Atreche L, Ayachi S, Ayadi I, Ayadi MA, Ayadi M, Ayari J, Ayed H, Ayed K, Ayedi H, Ayedi I, Azegrar M, Azzouz H, Babdalla F, Bachiri R, Bachiri Z, Baghdad M, Bahloul R, Bahouli A, Bahri M, Baississ I, Bakkali H, Balti M, Baraket O, Bargaoui H, Batti R, Bedioui A, Begag R, Behourah Z, Belaid I, Belaïd A, Ben Abdallah A, Ben Abdallah I, Ben Ahmed S, Ben Ahmed T, Ben Azaiz M, Ben Chehida MA, Ben Fatma L, Ben Ghachem D, Ben Ghachem T, Ben Hassouna J, Ben Hmida S, Ben Nasr S, Ben Nejima D, Ben Rahal K, Ben Rejeb M, Ben Rhouma S, Ben Safta I, Ben Salem A, Ben Zargouna Y, Benabdallah I, Benabdella H, Benabdessalem MZ, Benahmed K, Benahmed S, Benameur H, Benasr S, Benbrahim F, Benbrahim W, Benbrahim Z, Benchehida M, Bencheikh Y, Bendhiab T, Benfatma L, Bengueddach A, Benhami M, Benhassouna J, Benhbib W, Benjaafar N, Benkali R, Benkridis W, Benlaloui A, Benmaitig M, Benmansour A, Benmouhoub M, Benna F, Benna H, Benna M, Benna M, Bennabdellah H, Benrahal K, Bensafta I, Bensalah H, Bensalem A, Bensaud M, Benslama R, Benyoub M, Benzid K, Bergaoui H, Beroual M, Berrad S, Berrazaga Y, Bezzaz Z, Bhiri H, Bibi M, Binous MY, Blel A, Boder JM, Bouaouina N, Bouaziz H, Bouchoucha S, Boudawara T, Boudawara Z, Bouderbala A, Bouhali R, Bouhani M, Boujarnija R, Boujelben S, Boujelbene N, Boukerzaza I, Boukhari H, Boulfoul W, Boulma R, Boumansour N, Bouned A, Bounedjar A, Bouraoui I, Bouraoui S, Bourigua R, Bourmech M, Bousaffa H, Bousahba A, Bousrih C, Boussarsar A, Boussen H, Boutayeb S, Bouzaidi K, Bouzaiene F, Bouzaiene H, Bouzerzour Z, Bouzid K, Bouzid N, Bouzidi D, Bouzidi W, Bouzouita A, Brahimi S, Brahmia A, Buhmeida A, Chaaben K, Chaabouni H, Chaabouni M, Chaabène K, Chaari H, Chaari I, Chaari M, Chabchoub I, Chabeene K, Chaker K, Chakroun M, Charfi M, Charfi S, Chargui R, Charles M, Chebil M, Cheikchouk K, Chelly B, Chelly I, Cheraiet N, Cherif A, Cherif M, Cherifi A, Chikhrouhou T, Chikouche A, Chirouf A, Chraiet N, Collan Y, Cui Z, Dabbebi H, Daldoul A, Damouche I, Daoud H, Daoud N, Daoued J, Darif K, Darwish DO, Derbouz Z, Derouiche A, Dhibe TT, Dhibet T, Djallaoui A, Djami N, Djebbes K, Djedi H, Djeghim S, Djellali L, Djellaoui A, Djilat K, Djouabi R, Doumbia H, Drah M, Dridi M, Hsairi M, Elabbassi S, Elallia F, Elati Z, Elattassi M, Elbenna H, Elfagieh MA, Elfaitori O, Elfannas H, Elghali A, Elghali MA, Elgonti S, Elhadj OE, Elhazzaz R, Elkacemi H, Elkinany K, Elkissi Y, Elloumi F, Elmaalel O, Elmajjaou IS, Elmajjaoui S, Elmhabrech H, Elmrabet F, Elsaghayer WA, Elzagheid A, Emaetig F, Erraichi H, Essid M, Ewshah N, Ezzairi F, Faleh R, Fallah S, Farag AL, Farhat L, Fehri R, Feki J, Fendri S, Fendri S, Fessi Z, Filali T, Fissah A, Fourati M, Fourati N, Frikha M, Fuchs CS, Gabssi A, Gachi F, Gadria S, Gammoudi A, Ganzoui I, Gargoura A, Ghaddabb I, Gharbi I, Gharbi M, Ghazouani E, Gheriani N, Ghorbel A, Ghorbel L, Ghozi A, Ghrissi R, Gouader A, Goucha A, Guebsi A, Guellil I, Guermazi F, Guesmi S, Guetari W, Habak N, Haddad A, Haddad S, Haddaoui A, Hadef I, Hader AF, Hadiji A, Hadjarab F, Hadoussa M, Hadoussa N, Hafsa C, Hafsia M, Hajji A, Hajmansour M, Hamdi S, Hamici Z, Hamida S, Hamila F, Hamissa S, Hammouda B, Haouet S, Harhira I, Haroun A, Hassouni K, Hdiji A, Hechiche M, Hejjane L, Hellal C, Henni M, Herbegue K, Hichami L, Hikem M, Hmad A, Hmida L, Hmissa S, Hochlaf M, Houas A, Houhani M, Huwidi A, Ian C, Ibrahim BN, Ibrahim NY, Idir H, Issaoui D, Itaimi A, Izem AE, Jaidane O, Jamel D, Jamous H, Jarrar M, Jarrar MS, Jarray S, Jebsi M, Jmal H, Juwid A, Kaabia O, Kablouti A, Kacem I, Kacem K, Kaid MY, Kallel M, Kallel R, Kammoun H, Kari S, Karrit S, Kchir H, Kchir N, Kebdani T, Kechad N, Kehili H, Kerboua E, Keskes H, Kessi NN, Khababa N, Khaldi H, Khanfir A, Khater B, Khelif A, Khemiri S, Khennouf K, Khouni H, Khrouf S, Kmira Z, Kochbati L, Korbi A, Kouadri N, Kouhen F, Krarti M, Handoussa M, Hsu Y, Laakom O, Laato M, Labidi S, Lahlali F, Lahmidi A, Lalaoui A, Lamia N, Lamri A, Letaief F, Letaief MR, Aldehmani M, Rafael A, Liepa AM, Limaiem F, Limam K, Loughlimi H, Ltaief F, Maamouri N, Mabrouk M, Madouri R, Mahjoub N, Mahjoubi Z, Mahrsi M, Makrem H, Mallek W, Manitta M, Mansoura L, Mansouri H, Maoua M, Maoui W, Marouene C, Marzouk K, Masmoudi S, May F, Meddeb I, Meddeb K, Meddour S, Medhioub F, Mejri N, Melizi MR, Mellas N, Melliti R, Melzi A, Merair N, Merrouki FZ, Mersali C, Messalbi O, Messaoudi L, Messioud S, Messoudi K, Mestiri S, Mezlini A, Mezlini A, Mghirbi F, Mhabrech H, Mhiri A, Midoun N, Milud R, Missaoui B, Mnasser A, Mnejja W, Mokni M, Mokrani A, Mokrani M, Moujahed R, Moukasse Y, Mouzount A, Mrad K, Mraidha MH, Mrizak N, Mzali R, Mzid Y, M'ghirbi F, Nakhli A, Nasr C, Nasri S, Noubigh G, Nouha D, Nouia L, Nouira Y, Noureddine A, Nouri O, Ohtsu A, Ouahbi H, Oualla K, Ouanes Y, Ouaz H, Ouikene A, Ouldbessi N, Parker I, Pyrhonen S, Rachdi H, Rahal K, Rahal K, Rahoui M, Raies H, Rameh S, Reguieg K, Rejab H, Rejiba R, Rhim MS, Riahi S, Rouimel N, Saad Saoud N, Saadi K, Saadi M, Sadou A, Saguem I, Sahnoun T, Sahnoune H, Sakhri S, Sallemi A, Sassi A, Sbika W, Sedkaoui C, Sefiane S, Sellami A, Seppo P, Sfaoua H, Sghaier S, Shagan A, Siala W, Slim I, Slimene M, Soltani S, Souilah S, Souissi M, Sriha Badreddine B, Swaisi Y, Taibi A, Taktak T, Talbi G, Talha SW, Talima SM, Tbessi S, Tebani N, Tebra S, Tebramrad S, Telaijia D, Tenni A, Tolba A, Topov Y, Touil K, Toumi N, Toumi W, Tounsi N, Trigui A, Trigui R, Triki W, Walha M, Werda I, Yacoub H, Yahyaoui Y, Yaich A, Yaici R, Yamouni M, Yeddes I, Yekrou D, Yousfi M, Yousfi N, Youssfi MA, Zaabar L, Zaied S, Zaim I, Zakhama W, Zayed S, Zehani A, Zemni I, Zenzri Y, Zeraoula S, Zouiten O, Zoukar O, Zrafi W, Zribi A, Zubia N.

Tunis Med. 2018 Apr;96(4):177-182. No abstract available.

10.

Spontaneous Celiac Artery Dissection Presenting With Splenic Infarction: A Case Report.

Abugroun A, Natarajan A, Daoud H, Khalaf H.

Gastroenterology Res. 2018 Oct;11(5):379-382. doi: 10.14740/gr1065w. Epub 2018 Oct 1.

11.

Isolated Superior Mesenteric Artery Dissection: A Case Report and Literature Review.

Daoud H, Abugroun A, Subahi A, Khalaf H.

Gastroenterology Res. 2018 Oct;11(5):374-378. doi: 10.14740/gr1056w. Epub 2018 Oct 1.

12.

Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension.

McDonell LM, Leung GK, Daoud H, Ip J, Chim S, Luk HM, Lan L; Care4Rare Canada Consortium, Boycott KM, Chung BH.

Am J Med Genet A. 2018 Nov;176(11):2523-2527. doi: 10.1002/ajmg.a.40349. Epub 2018 Oct 5. No abstract available.

PMID:
30289595
13.

Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory.

Nfonsam L, Ordorica S, Ghani M, Potter R, Schaffer A, Daoud H, Vasli N, Chisholm C, Sinclair-Bourque E, McGowan-Jordan J, Smith AC, Jarinova O, Bronicki L.

J Med Genet. 2019 Jun;56(6):408-412. doi: 10.1136/jmedgenet-2018-105443. Epub 2018 Sep 21.

PMID:
30242101
14.

Bordetella holmesii Contamination of Platelet Concentrates: Revisiting the Definition of a Positive Culture.

Cloutier M, Nolin MÈ, Daoud H, Jacques A, de Grandmont MJ, Ducas É, Delage G, Thibault L.

J Clin Microbiol. 2018 Nov 27;56(12). pii: e01105-18. doi: 10.1128/JCM.01105-18. Print 2018 Dec.

15.

SLAMM: Visual monocular SLAM with continuous mapping using multiple maps.

Daoud HA, Md Sabri AQ, Loo CK, Mansoor AM.

PLoS One. 2018 Apr 27;13(4):e0195878. doi: 10.1371/journal.pone.0195878. eCollection 2018.

16.

Reinterpretation of sequence variants: one diagnostic laboratory's experience, and the need for standard guidelines.

Chisholm C, Daoud H, Ghani M, Mettler G, McGowan-Jordan J, Sinclair-Bourque L, Smith A, Jarinova O.

Genet Med. 2018 Mar;20(3):365-368. doi: 10.1038/gim.2017.191. Epub 2017 Dec 14.

PMID:
29240080
17.

Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).

Lebo MS, Zakoor KR, Chun K, Speevak MD, Waye JS, McCready E, Parboosingh JS, Lamont RE, Feilotter H, Bosdet I, Tucker T, Young S, Karsan A, Charames GS, Agatep R, Spriggs EL, Chisholm C, Vasli N, Daoud H, Jarinova O, Tomaszewski R, Hume S, Taylor S, Akbari MR, Lerner-Ellis J; Canadian Open Genetics Repository Working Group.

Genet Med. 2018 Mar;20(3):294-302. doi: 10.1038/gim.2017.80. Epub 2017 Jul 20.

PMID:
28726806
18.

Compression of high-density 0.16 pC electron bunches through high field gradients for ultrafast single shot electron diffraction: The Compact RF Gun.

Daoud H, Floettmann K, Dwayne Miller RJ.

Struct Dyn. 2017 Apr 12;4(4):044016. doi: 10.1063/1.4979970. eCollection 2017 Jul.

19.

ATXN2 trinucleotide repeat length correlates with risk of ALS.

Sproviero W, Shatunov A, Stahl D, Shoai M, van Rheenen W, Jones AR, Al-Sarraj S, Andersen PM, Bonini NM, Conforti FL, Van Damme P, Daoud H, Del Mar Amador M, Fogh I, Forzan M, Gaastra B, Gellera C, Gitler AD, Hardy J, Fratta P, La Bella V, Le Ber I, Van Langenhove T, Lattante S, Lee YC, Malaspina A, Meininger V, Millecamps S, Orrell R, Rademakers R, Robberecht W, Rouleau G, Ross OA, Salachas F, Sidle K, Smith BN, Soong BW, Sorarù G, Stevanin G, Kabashi E, Troakes C, van Broeckhoven C, Veldink JH, van den Berg LH, Shaw CE, Powell JF, Al-Chalabi A.

Neurobiol Aging. 2017 Mar;51:178.e1-178.e9. doi: 10.1016/j.neurobiolaging.2016.11.010. Epub 2016 Nov 24.

20.

Combined Genotype Analyses of Precursor miRNA196a2 and 499a Variants with Hepatic and Renal Cancer Susceptibility a Preliminary Study.

Toraih EA, Fawz MS, Elgazzaz MG, Hussein MH, Shehata RH, Daoud HG.

Asian Pac J Cancer Prev. 2016;17(7):3369-75.

21.

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.

Daoud H, Luco SM, Li R, Bareke E, Beaulieu C, Jarinova O, Carson N, Nikkel SM, Graham GE, Richer J, Armour C, Bulman DE, Chakraborty P, Geraghty M, Lines MA, Lacaze-Masmonteil T, Majewski J, Boycott KM, Dyment DA.

CMAJ. 2016 Aug 9;188(11):E254-E260. doi: 10.1503/cmaj.150823. Epub 2016 May 30.

22.

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

Williams KL, Topp S, Yang S, Smith B, Fifita JA, Warraich ST, Zhang KY, Farrawell N, Vance C, Hu X, Chesi A, Leblond CS, Lee A, Rayner SL, Sundaramoorthy V, Dobson-Stone C, Molloy MP, van Blitterswijk M, Dickson DW, Petersen RC, Graff-Radford NR, Boeve BF, Murray ME, Pottier C, Don E, Winnick C, McCann EP, Hogan A, Daoud H, Levert A, Dion PA, Mitsui J, Ishiura H, Takahashi Y, Goto J, Kost J, Gellera C, Gkazi AS, Miller J, Stockton J, Brooks WS, Boundy K, Polak M, Muñoz-Blanco JL, Esteban-Pérez J, Rábano A, Hardiman O, Morrison KE, Ticozzi N, Silani V, de Belleroche J, Glass JD, Kwok JB, Guillemin GJ, Chung RS, Tsuji S, Brown RH Jr, García-Redondo A, Rademakers R, Landers JE, Gitler AD, Rouleau GA, Cole NJ, Yerbury JJ, Atkin JD, Shaw CE, Nicholson GA, Blair IP.

Nat Commun. 2016 Apr 15;7:11253. doi: 10.1038/ncomms11253.

23.

Evaluation of Spirulina platensis extract as natural antivirus against foot and mouth disease virus strains (A, O, SAT2).

Daoud HM, Soliman EM.

Vet World. 2015 Oct;8(10):1260-5. doi: 10.14202/vetworld.2015.1260-1265. Epub 2015 Oct 31.

24.

Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature.

Luco SM, Pohl D, Sell E, Wagner JD, Dyment DA, Daoud H.

BMC Med Genet. 2016 Feb 27;17:15. doi: 10.1186/s12881-016-0276-4. Review.

25.

Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.

Richer J, Daoud H, Geier P, Jarinova O, Carson N, Feberova J, Ben Fadel N, Unrau J, Bareke E, Khatchadourian K, Bulman DE, Majewski J, Boycott KM, Dyment DA.

Am J Med Genet A. 2015 Nov;167A(11):2867. doi: 10.1002/ajmg.a.37270. Epub 2015 Aug 26. No abstract available.

PMID:
26480306
26.

Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion.

Antoun G, McBride S, Vanstone JR, Naas T, Michaud J, Redpath S, McMillan HJ, Brophy J, Daoud H, Chakraborty P, Dyment D, Holcik M, Harper ME, Lines MA.

JIMD Rep. 2016;27:1-9. doi: 10.1007/8904_2015_491. Epub 2015 Sep 25.

27.

Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay.

Daoud H, Zhang D, McMurray F, Yu A, Luco SM, Vanstone J, Jarinova O, Carson N, Wickens J, Shishodia S, Choi H, McDonough MA, Schofield CJ, Harper ME, Dyment DA, Armour CM.

J Med Genet. 2016 Mar;53(3):200-7. doi: 10.1136/jmedgenet-2015-103399. Epub 2015 Sep 16.

PMID:
26378117
28.

Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia.

Daoud H, Papadima EM, Ouled Amar Bencheikh B, Katsila T, Dionne-Laporte A, Spiegelman D, Dion PA, Patrinos GP, Orrù S, Rouleau GA.

Eur J Med Genet. 2015 Nov;58(11):573-7. doi: 10.1016/j.ejmg.2015.08.001. Epub 2015 Aug 7.

PMID:
26260707
29.

Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum.

Jouan L, Ouled Amar Bencheikh B, Daoud H, Dionne-Laporte A, Dobrzeniecka S, Spiegelman D, Rochefort D, Hince P, Szuto A, Lassonde M, Barbelanne M, Tsang WY, Dion PA, Théoret H, Rouleau GA.

Eur J Hum Genet. 2016 Apr;24(4):607-10. doi: 10.1038/ejhg.2015.156. Epub 2015 Jul 22.

30.

Influence of W, Mo and Ti trace elements on the phase separation in Al8Co17Cr17Cu8Fe17Ni33 based high entropy alloy.

Manzoni AM, Daoud HM, Voelkl R, Glatzel U, Wanderka N.

Ultramicroscopy. 2015 Dec;159 Pt 2:265-71. doi: 10.1016/j.ultramic.2015.06.009. Epub 2015 Jun 14.

PMID:
26159736
31.

Basal skull fractures are associated with mortality in pediatric severe traumatic brain injury.

Alhelali I, Stewart TC, Foster J, Alharfi IM, Ranger A, Daoud H, Fraser DD.

J Trauma Acute Care Surg. 2015 Jun;78(6):1155-61. doi: 10.1097/TA.0000000000000662.

PMID:
26151517
32.

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population.

Amy M, Staehlin O, René F, Blasco H, Marouillat S, Daoud H, Vourc'h P, Gordon PH, Camu W, Corcia P, Loeffler JP, Palkovits M, Sommer WH, Andres CR.

Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(7-8):490-6. doi: 10.3109/21678421.2015.1051988. Epub 2015 Jun 17.

PMID:
26083872
33.

Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients.

Gonzalez-Perez P, Woehlbier U, Chian RJ, Sapp P, Rouleau GA, Leblond CS, Daoud H, Dion PA, Landers JE, Hetz C, Brown RH.

Gene. 2015 Jul 25;566(2):158-65. doi: 10.1016/j.gene.2015.04.035. Epub 2015 Apr 22.

34.

Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.

Richer J, Daoud H, Geier P, Jarinova O, Carson N, Feberova J, Ben Fadel N, Unrau J, Bareke E, Khatchadourian K, Bulman DE, Majewski J, Boycott KM, Dyment DA.

Am J Med Genet A. 2015 Jul;167(7):1654-8. doi: 10.1002/ajmg.a.37067. Epub 2015 Apr 21. Erratum in: Am J Med Genet A. 2015 Nov;167A(11):2867. Fadfel, Nadya Ben [corrected to Ben Fadel, Nadya].

PMID:
25899979
35.

C9orf72 repeat expansions in rapid eye movement sleep behaviour disorder.

Daoud H, Postuma RB, Bourassa CV, Rochefort D, Gauthier MT, Montplaisir J, Gagnon JF, Arnulf I, Dauvilliers Y, Charley CM, Inoue Y, Sasai T, Högl B, Desautels A, Frauscher B, Cochen De Cock V, Rouleau GA, Dion PA.

Can J Neurol Sci. 2014 Nov;41(6):759-62. doi: 10.1017/cjn.2014.39. Epub 2014 Nov 4.

PMID:
25377888
36.

De novo mutations in moderate or severe intellectual disability.

Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL.

PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct.

37.

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

Kaneb HM, Folkmann AW, Belzil VV, Jao LE, Leblond CS, Girard SL, Daoud H, Noreau A, Rochefort D, Hince P, Szuto A, Levert A, Vidal S, André-Guimont C, Camu W, Bouchard JP, Dupré N, Rouleau GA, Wente SR, Dion PA.

Hum Mol Genet. 2015 Mar 1;24(5):1363-73. doi: 10.1093/hmg/ddu545. Epub 2014 Oct 24.

38.

Early critical care course in children after liver transplant.

Kukreti V, Daoud H, Bola SS, Singh RN, Atkison P, Kornecki A.

Crit Care Res Pract. 2014;2014:725748. doi: 10.1155/2014/725748. Epub 2014 Sep 25.

39.

A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories.

Akimoto C, Volk AE, van Blitterswijk M, Van den Broeck M, Leblond CS, Lumbroso S, Camu W, Neitzel B, Onodera O, van Rheenen W, Pinto S, Weber M, Smith B, Proven M, Talbot K, Keagle P, Chesi A, Ratti A, van der Zee J, Alstermark H, Birve A, Calini D, Nordin A, Tradowsky DC, Just W, Daoud H, Angerbauer S, DeJesus-Hernandez M, Konno T, Lloyd-Jani A, de Carvalho M, Mouzat K, Landers JE, Veldink JH, Silani V, Gitler AD, Shaw CE, Rouleau GA, van den Berg LH, Van Broeckhoven C, Rademakers R, Andersen PM, Kubisch C.

J Med Genet. 2014 Jun;51(6):419-24. doi: 10.1136/jmedgenet-2014-102360. Epub 2014 Apr 4.

40.

Infection rates, fevers, and associated factors in pediatric severe traumatic brain injury.

Alharfi IM, Charyk Stewart T, Al Helali I, Daoud H, Fraser DD.

J Neurotrauma. 2014 Mar 1;31(5):452-8. doi: 10.1089/neu.2013.2904. Epub 2013 Dec 19.

PMID:
24093309
41.

New bacteriocin from Bacillus clausii strainGM17: purification, characterization, and biological activity.

Mouloud G, Daoud H, Bassem J, Laribi Atef I, Hani B.

Appl Biochem Biotechnol. 2013 Dec;171(8):2186-200. doi: 10.1007/s12010-013-0489-3. Epub 2013 Sep 14.

PMID:
24037515
42.

Brain injury biomarkers as outcome predictors in pediatric severe traumatic brain injury.

Daoud H, Alharfi I, Alhelali I, Charyk Stewart T, Qasem H, Fraser DD.

Neurocrit Care. 2014 Jun;20(3):427-35. doi: 10.1007/s12028-013-9879-1. Review.

PMID:
23943317
43.

Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.

Daoud H, Tétreault M, Gibson W, Guerrero K, Cohen A, Gburek-Augustat J, Synofzik M, Brais B, Stevens CA, Sanchez-Carpintero R, Goizet C, Naidu S, Vanderver A, Bernard G.

J Med Genet. 2013 Mar;50(3):194-7. doi: 10.1136/jmedgenet-2012-101357. Epub 2013 Jan 25.

PMID:
23355746
44.

Phase separation in equiatomic AlCoCrFeNi high-entropy alloy.

Manzoni A, Daoud H, Völkl R, Glatzel U, Wanderka N.

Ultramicroscopy. 2013 Sep;132:212-5. doi: 10.1016/j.ultramic.2012.12.015. Epub 2012 Dec 20.

PMID:
23352803
45.

Investigation of C9orf72 repeat expansions in Parkinson's disease.

Daoud H, Noreau A, Rochefort D, Paquin-Lanthier G, Gauthier MT, Provencher P, Pourcher E, Dupré N, Chouinard S, Jodoin N, Soland V, Fon EA, Dion PA, Rouleau GA.

Neurobiol Aging. 2013 Jun;34(6):1710.e7-9. doi: 10.1016/j.neurobiolaging.2012.11.025. Epub 2012 Dec 27.

PMID:
23273600
46.

Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.

Daoud H, Dobrzeniecka S, Camu W, Meininger V, Dupré N, Dion PA, Rouleau GA.

Neurobiol Aging. 2013 Apr;34(4):1311.e1-2. doi: 10.1016/j.neurobiolaging.2012.09.001. Epub 2012 Oct 10.

PMID:
23062600
47.

A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome.

Vu PY, Toutain J, Cappellen D, Delrue MA, Daoud H, El Moneim AA, Barat P, Montaubin O, Bonnet F, Dai ZQ, Philippe C, Tran CT, Rooryck C, Arveiler B, Saura R, Briault S, Lacombe D, Taine L.

Am J Med Genet A. 2012 Nov;158A(11):2849-56. doi: 10.1002/ajmg.a.35694. Epub 2012 Oct 3.

PMID:
23034868
48.

C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia.

Daoud H, Suhail H, Sabbagh M, Belzil V, Szuto A, Dionne-Laporte A, Khoris J, Camu W, Salachas F, Meininger V, Mathieu J, Strong M, Dion PA, Rouleau GA.

Arch Neurol. 2012 Sep;69(9):1159-63. doi: 10.1001/archneurol.2012.377.

PMID:
22964911
49.

Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia.

Belzil VV, Daoud H, Camu W, Strong MJ, Dion PA, Rouleau GA.

Eur J Hum Genet. 2013 Feb;21(2):237-9. doi: 10.1038/ejhg.2012.135. Epub 2012 Jun 27.

50.

Parent-child exome sequencing identifies a de novo truncating mutation in TCF4 in non-syndromic intellectual disability.

Hamdan FF, Daoud H, Patry L, Dionne-Laporte A, Spiegelman D, Dobrzeniecka S, Rouleau GA, Michaud JL.

Clin Genet. 2013 Feb;83(2):198-200. doi: 10.1111/j.1399-0004.2012.01890.x. Epub 2012 Jun 4. No abstract available.

PMID:
22670824

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