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34 results for Haghighi,+Alireza

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ArticlesPeer ReviewedFull Text
Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy
Author / Creator:Hinson, John T. ; Chopra, Anant ; Nafissi, Navid ; Polacheck, William J. ; Benson, Craig C. ; Swist, Sandra ; Gorham, Joshua ; Yang, Luhan ; Schafer, Sebastian ; Sheng, Calvin C. ; Haghighi, Alireza ; Homsy, Jason ; Hubner, Norbert ; Church, George ; Cook, Stuart A. ; Linke, Wolfgang A. ; Chen, Christopher S. ; Seidman, J. G. ; Seidman, Christine E.
Publisher:Washington: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2015-08, Vol.349 (6251), p.982-986
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ArticlesPeer ReviewedFull Text
State of the Art in the Optimisation of Wind Turbine Performance Using CFD
Author / Creator:Shourangiz-Haghighi, Alireza ; Mohammad Amin Haghnegahdar ; Wang, Lin ; Mussetta, Marco ; Kolios, Athanasios ; Lander, Martin
Publisher:Dordrecht: Springer Nature B.V
Journal title:Archives of computational methods in engineering, 2020-04, p.1-19
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ArticlesPeer ReviewedFull Text
Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy
Author / Creator:Jain, Pratul Kumar ; Jayappa, Shashank ; Sairam, Thiagarajan ; Mittal, Anupam ; Paul, Sayan ; Rao, Vinay J ; Chittora, Harshil ; Kashyap, Deepak K ; Palakodeti, Dasaradhi ; Thangaraj, Kumarasamy ; Shenthar, Jayaprakash ; Koranchery, Rakesh ; Rajendran, Ranjith ; Alireza, Haghighi ; Mohanan, Kurukkanparampil Sreedharan ; Rathinavel, Andiappan ; Dhandapany, Perundurai S
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2022-10, Vol.59 (10), p.984-992
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Newsletter articlesFull Text
World Cup 2014: Lionel Messi grabs injury-time winner as Argentina beats Iran 1-0 in Belo Horizonte to qualify for next round; Lionel Messi left it late as Argentina beat a courageous Iran side 1-0 in...
Publisher:Sydney: Australian Broadcasting Corporation
Journal title:ABC Premium News, 2014
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A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Author / Creator:Horvat, Claire ; Johnson, Renee ; Lam, Lien ; Munro, Jacob ; Mazzarotto, Francesco ; Roberts, Angharad M. ; Herman, Daniel S. ; Parfenov, Michael ; Haghighi, Alireza ; McDonough, Barbara ; DePalma, Steven R. ; Keogh, Anne M. ; Macdonald, Peter S. ; Hayward, Christopher S. ; Roberts, Amy ; Barton, Paul J.R. ; Felkin, Leanne E. ; Giannoulatou, Eleni ; Cook, Stuart A. ; Seidman, J.G. ; Seidman, Christine E. ; Fatkin, Diane
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2019-01, Vol.21 (1), p.133-143
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ArticlesPeer ReviewedFull Text
Bridging silicon and carbon worlds with digital twins and on-chip systems in drug discovery
Author / Creator:Akbarialiabad, Hossein ; Seyyedi, Mahdiyeh Sadat ; Paydar, Shahram ; Habibzadeh, Adrina ; Haghighi, Alireza ; Kvedar, Joseph C.
Publisher:London: Nature Publishing Group UK
Journal title:NPJ systems biology and applications, 2024-12, Vol.10 (1), p.150-6, Article 150
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ArticlesPeer ReviewedFull Text
Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis
Author / Creator:Hildebrandt, Jenna ; Yalcin, Ebru ; Bresser, Hans-Georg ; Cinel, Guzin ; Gappa, Monika ; Haghighi, Alireza ; Kiper, Nural ; Khalilzadeh, Soheila ; Reiter, Karl ; Sayer, John ; Schwerk, Nicolaus ; Sibbersen, Anke ; Van Daele, Sabine ; Nübling, Georg ; Lohse, Peter ; Griese, Matthias
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2014-11, Vol.9 (1), p.171-171, Article 171
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ArticlesPeer ReviewedFull Text
A Missense Mutation in the MBTPS2 Gene Underlies the X-Linked Form of Olmsted Syndrome
Author / Creator:Haghighi, Alireza ; Scott, Claire A. ; Poon, Daniel S. ; Yaghoobi, Reza ; Saleh-Gohari, Nasrollah ; Plagnol, Vincent ; Kelsell, David P.
Publisher:United States: Elsevier Inc
Journal title:Journal of investigative dermatology, 2013-02, Vol.133 (2), p.571-573
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ArticlesPeer ReviewedFull Text
Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome
Author / Creator:Haghighi, Alireza ; Tiwari, Amit ; Piri, Niloofar ; Nürnberg, Gudrun ; Saleh-Gohari, Nasrollah ; Haghighi, Amirreza ; Neidhardt, John ; Nürnberg, Peter ; Berger, Wolfgang
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-11, Vol.9 (11), p.e112747-e112747
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ArticlesPeer ReviewedFull Text
Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age
Author / Creator:Brownstein, Catherine A. ; Douard, Elise ; Haynes, Robin L. ; Koh, Hyun Yong ; Haghighi, Alireza ; Keywan, Christine ; Martin, Bree ; Alexandrescu, Sanda ; Haas, Elisabeth A. ; Vargas, Sara O. ; Wojcik, Monica H. ; Jacquemont, Sébastien ; Poduri, Annapurna H. ; Goldstein, Richard D. ; Holm, Ingrid A.
Publisher:United States: John Wiley & Sons, Inc
Journal title:Genetics & genomics next, 2023-03, Vol.4 (1), p.2200012-n/a
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ArticlesPeer ReviewedFull Text
Identification of two HEXA mutations causing infantile-onset Tay–Sachs disease in the Persian population
Author / Creator:Haghighi, Alireza ; Rezazadeh, Jamileh ; Shadmehri, Azam Ahmadi ; Haghighi, Amirreza ; Kornreich, Ruth ; Desnick, Robert J
Publisher:London: Nature Publishing Group UK
Journal title:Journal of human genetics, 2011-09, Vol.56 (9), p.682-684
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ArticlesPeer ReviewedFull Text
Aripiprazole Versus Risperidone for Treating Children and Adolescents with Tic Disorder: A Randomized Double Blind Clinical Trial
Author / Creator:Ghanizadeh, Ahmad ; Haghighi, Alireza
Publisher:Boston: Springer US
Journal title:Child psychiatry and human development, 2014-10, Vol.45 (5), p.596-603
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ArticlesPeer ReviewedFull Text
The "Velvet Revolution" of Iranian Puritan Hardliners: Mahmoud Ahmadinejad's Rise to Power
Author / Creator:Haghighi, Alireza N. ; Tahmasebi, Victoria
Publisher:London, England: Canadian Institute of International Affairs
Journal title:International journal (Toronto), 2006-12, Vol.61 (4), p.959-970
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ArticlesPeer ReviewedFull Text
The “Velvet Revolution” of Iranian Puritan Hardliners
Author / Creator:Haghighi, Alireza N ; Tahmasebi, Victoria
Publisher:Toronto: Sage Publications Ltd
Journal title:International journal (Toronto), 2006-12, Vol.61 (4), p.959-970
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ArticlesPeer ReviewedFull Text
Nemaline myopathy: reclassification of previously reported variants according to ACMG guidelines, and report of novel genetic variants
Author / Creator:Haghighi, Alireza ; Alvandi, Zahra ; Nilipour, Yalda ; Haghighi, Amirreza ; Kornreich, Ruth ; Nafissi, Shahriar ; Desnick, Robert J.
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2023-11, Vol.31 (11), p.1237-1250
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ArticlesPeer ReviewedFull Text
Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans
Author / Creator:Lee, Vivian S. ; Halabi, Carmen M. ; Hoffman, Erin P. ; Carmichael, Nikkola ; Leshchiner, Ignaty ; Lian, Christine G. ; Bierhals, Andrew J. ; Vuzman, Dana ; Medicine, Brigham Genomic ; Mecham, Robert P. ; Frank, Natasha Y. ; Stitziel, Nathan O.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2016-08, Vol.113 (31), p.8759-8764
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ArticlesPeer ReviewedFull Text
Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome
Author / Creator:Habeb, Abdelhadi M. ; Flanagan, Sarah E. ; Zulali, Mohamed A. ; Abdullah, Mohamed A. ; Pomahačová, Renata ; Boyadzhiev, Veselin ; Colindres, Lesby E. ; Godoy, Guillermo V. ; Vasanthi, Thiruvengadam ; Al Saif, Ramlah ; Setoodeh, Aria ; Haghighi, Amirreza ; Haghighi, Alireza ; Shaalan, Yomna ; Hattersley, Andrew T. ; Ellard, Sian ; De Franco, Elisa
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Diabetologia, 2018-05, Vol.61 (5), p.1027-1036
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ArticlesPeer ReviewedFull Text
Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants
Author / Creator:Herkert, Johanna C. ; Verhagen, Judith M.A. ; Yotti, Raquel ; Haghighi, Alireza ; Phelan, Dean G. ; James, Paul A. ; Brown, Natasha J. ; Stutterd, Chloe ; Macciocca, Ivan ; Leong, Kai'En ; Bulthuis, Marian L.C. ; van Bever, Yolande ; van Slegtenhorst, Marjon A. ; Boven, Ludolf G. ; Roberts, Amy E. ; Agarwal, Radhika ; Seidman, Jonathan ; Lakdawala, Neal K. ; Fernández-Avilés, Francisco ; Burke, Michael A. ; Pierpont, Mary Ella ; Braunlin, Elizabeth ; Ḉağlayan, Ahmet Okay ; Barge-Schaapveld, Daniela Q.C.M. ; Birnie, Erwin ; van Osch-Gevers, Lennie ; van Langen, Irene M. ; Jongbloed, Jan D.H. ; Lockhart, Paul J. ; Amor, David J. ; Seidman, Christine E. ; van de Laar, Ingrid M.B.H.
Publisher:United States: Elsevier Inc
Journal title:The American heart journal, 2020-07, Vol.225, p.108-119
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ArticlesPeer ReviewedFull Text
Genetics of GNE myopathy in the non-Jewish Persian population
Author / Creator:Haghighi, Alireza ; Nafissi, Shahriar ; Qurashi, Abrar ; Tan, Zheng ; Shamshiri, Hosein ; Nilipour, Yalda ; Haghighi, Amirreza ; Desnick, Robert J ; Kornreich, Ruth
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2016-02, Vol.24 (2), p.243-251
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ArticlesPeer ReviewedFull Text
Association of Parental Consanguinity With Papillary Thyroid Carcinoma: A Case-Control Study
Author / Creator:Zayed, Ayman A ; Amarin, Justin Z ; Al-Ani, Abdallah T ; Altell, Tareq L ; Abdelhamid, Sultan S ; Qirem, Murad M ; Fahmawi, Suhib M ; Elshebli, Sanad M ; Hamo, Khair M ; Zaghlol, Louay Y ; Tierney, Michael E ; Zayed, Jana A ; Haghighi, Alireza
Publisher:US: Oxford University Press
Journal title:The journal of clinical endocrinology and metabolism, 2021-07, Vol.106 (7), p.e2769-e2774
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Showing 1 to 20 of 34 results

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Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy

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State of the Art in the Optimisation of Wind Turbine Performance Using CFD

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Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy

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World Cup 2014: Lionel Messi grabs injury-time winner as Argentina beats Iran 1-0 in Belo Horizonte to qualify for next round; Lionel Messi left it late as Argentina beat a courageous Iran side 1-0 in...

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A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy

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Bridging silicon and carbon worlds with digital twins and on-chip systems in drug discovery

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Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis

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A Missense Mutation in the MBTPS2 Gene Underlies the X-Linked Form of Olmsted Syndrome

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Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome

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Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age

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Identification of two HEXA mutations causing infantile-onset Tay–Sachs disease in the Persian population

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Aripiprazole Versus Risperidone for Treating Children and Adolescents with Tic Disorder: A Randomized Double Blind Clinical Trial

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The "Velvet Revolution" of Iranian Puritan Hardliners: Mahmoud Ahmadinejad's Rise to Power

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The “Velvet Revolution” of Iranian Puritan Hardliners

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Nemaline myopathy: reclassification of previously reported variants according to ACMG guidelines, and report of novel genetic variants

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Loss of function mutation in LOX causes thoracic aortic aneurysm and dissection in humans

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Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome

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Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants

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Genetics of GNE myopathy in the non-Jewish Persian population

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Association of Parental Consanguinity With Papillary Thyroid Carcinoma: A Case-Control Study

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