Garshasbi, S.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Strategies to Manage the Impacts of the COVID-19 Pandemic in the Supply Chain: Implications for Improving Economic and Social Sustainability

Taqi, Hasin Md. Muhtasim, Ahmed, Humaira Nafisa, Paul, Sumit, Garshasbi, Maryam, Ali, Syed Mithun, Kabir, Golam, Paul, Sanjoy Kumar

Journal:

Year:

2020

File:

PDF, 2.06 MB

2020

2

Study on the removal of heavy metal ions from industry waste by carbon nanotubes: effect of the surface modification-A review

Gupta, V. K., Tyagi, I., Agarwal, S., Moradi, O., Sadegh, H., Shahryari-ghoshekandi, R., Makhlouf, A. S. H., Goodarzi, M., Garshasbi, A.

Journal:

Critical Reviews in Environmental Science and Technology

Year:

2015

Language:

english

File:

PDF, 1.16 MB

english, 2015

3

Multi-Objective Optimization of Building Envelope Design for Life Cycle Environmental Performance

Azari, Rahman, Garshasbi, Samira, Amini, Pegah, Rashed-Ali, Hazem, Mohammadi, Yousef

Journal:

Energy and Buildings

Year:

2016

Language:

english

File:

PDF, 1.44 MB

english, 2016

4

The sociology of emotions of the protest action of Iranians on 28 December 2017

Karimi Malh, Ali, Garshasbi, Reza

Journal:

Asian Journal of Political Science

Year:

2020

File:

PDF, 2.58 MB

2020

5

Critical success factors for implementing green supply chain management in the electronics industry: an emerging economy case

Banik, Amit, Taqi, Hasin Md. Muhtasim, Ali, Syed Mithun, Ahmed, Sayem, Garshasbi, Maryam, Kabir, Golam

Journal:

International Journal of Logistics

Year:

2020

File:

PDF, 2.80 MB

2020

6

ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions

Hao Hu, Katinka Eggers, Wei Chen, Masoud Garshasbi, M. Mahdi Motazacker, Klaus Wrogemann, Kimia Kahrizi, Andreas Tzschach, Masoumeh Hosseini, Ideh Bahman, Tim Hucho, Martina Mühlenhoff, Rita Gerardy-S

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 511 KB

english, 2011

7

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Najmabadi, Hossein, Hu, Hao, Garshasbi, Masoud, Zemojtel, Tomasz, Abedini, Seyedeh Sedigheh, Chen, Wei, Hosseini, Masoumeh, Behjati, Farkhondeh, Haas, Stefan, Jamali, Payman

Journal:

Year:

2011

Language:

english

File:

PDF, 192 KB

english, 2011

8

The effect of exercise on the intensity of low back pain in pregnant women

A. Garshasbi, S. Faghih Zadeh

Journal:

International Journal of Gynecology & Obstetrics

Year:

2005

Language:

english

File:

PDF, 82 KB

english, 2005

9

Cohen syndrome diagnosis using whole genome arrays

Rivera-Brugues, N., Albrecht, B., Wieczorek, D., Schmidt, H., Keller, T., Gohring, I., Ekici, A. B., Tzschach, A., Garshasbi, M., Franke, K., Klopp, N., Wichmann, H.-E., Meitinger, T., Strom, T. M., H

Journal:

Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 408 KB

english, 2011

10

Equilibrium CO2 adsorption on zeolite 13X prepared from natural clays

Garshasbi, Vahid, Jahangiri, Mansour, Anbia, Mansoor

Journal:

Applied Surface Science

Year:

2017

Language:

english

File:

PDF, 2.31 MB

english, 2017

11

Isolated Congenital Anosmia and CNGA2 Mutation

Sailani, M. Reza, Jingga, Inlora, MirMazlomi, Seyed Hashem, Bitarafan, Fatemeh, Bernstein, Jonathan A., Snyder, Michael P., Garshasbi, Masoud

Journal:

Scientific Reports

Year:

2017

Language:

english

File:

PDF, 1.63 MB

english, 2017

12

Leptospirosis in Caspian Sea littoral, Gilan Province, Iran

Garshasbi, Vahid, Naddaf, Saied Reza, Aghighi, Zohreh, Hassan, Nayerreh, Pooya, Mohammad, Mostafavi, Ehsan

Journal:

Year:

2018

Language:

english

File:

PDF, 408 KB

english, 2018

13

Optimal Learning Group Formation: A Multi-objective Heuristic Search Strategy for Enhancing Inter-group Homogeneity and Intra-group Heterogeneity

Garshasbi, Soheila, Mohammadi, Yousef, Graf, Sabine, Garshasbi, Samira, Shen, Jun

Journal:

Expert Systems with Applications

Year:

2018

Language:

english

File:

PDF, 8.48 MB

english, 2018

14

Evaluating the Impact of Information Technology on Knowledge Management Performance with Balance Scorecard Approach

Siadat, Seyed Hossein, Abdollahi, Ali, Garshasbi, Laleh

Journal:

International Journal of Knowledge-Based Organizations

Year:

2017

Language:

english

File:

PDF, 477 KB

english, 2017

15

Using advanced thermochromic technologies in the built environment: Recent development and potential to decrease the energy consumption and fight urban overheating

Garshasbi, Samira, Santamouris, Mat

Journal:

Solar Energy Materials and Solar Cells

Year:

2019

Language:

english

File:

PDF, 1.24 MB

english, 2019

16

RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant

Kameli, Reyhaneh, Amanat, Man, Rezaei, Zahra, Hosseionpour, Sareh, Nikbakht, Sedigheh, Alizadeh, Houman, Ashrafi, Mahmoud Reza, Omrani, Abdolmajid, Garshasbi, Masoud, Tavasoli, Ali Reza

Journal:

Orphanet Journal of Rare Diseases

Year:

2019

Language:

english

File:

PDF, 2.20 MB

english, 2019

17

Boundary functions determination in an inverse time fractional heat conduction problem

Toubaei, S., Garshasbi, M., Reihani, P.

Journal:

Computational & Applied Mathematics

Year:

2019

Language:

english

File:

PDF, 6.29 MB

english, 2019

18

Compound Heterozygous Mutations in PNKP Gene in an Iranian Child with Microcephaly, Seizures, and Developmental Delay

Bitarafan, Fatemeh, Khodaeian, Mehrnoosh, Almadani, Navid, Kalhor, Alireza, Sardehaei, Elham Amjadi, Garshasbi, Masoud

Journal:

Fetal and Pediatric Pathology

Year:

2019

Language:

english

File:

PDF, 999 KB

english, 2019

19

A novel missense variant in GPT2 causes non-syndromic autosomal recessive intellectual disability in a consanguineous Iranian family

Binaafar, Sima, Razmara, Ehsan, Mahdieh, Nejat, Sahebjame, Hamidreza, Tavasoli, Alireza, Garshasbi, Masoud

Journal:

European Journal of Medical Genetics

Year:

2020

Language:

english

File:

PDF, 3.27 MB

english, 2020

20

Can quantum dots help to mitigate urban overheating? An experimental and modelling study

Garshasbi, Samira, Huang, Shujuan, Valenta, Jan, Santamouris, Mat

Journal:

Year:

2020

File:

PDF, 1.17 MB

2020

21

On the combination of quantum dots with near-infrared reflective base coats to maximize their urban overheating mitigation potential

Garshasbi, Samira, Huang, Shujuan, Valenta, Jan, Santamouris, Mat

Journal:

Year:

2020

File:

PDF, 1.41 MB

2020

22

[IEEE 2019 Iranian Conference on Renewable Energy & Distributed Generation (ICREDG) - Tehran, Iran (2019.6.11-2019.6.12)] 2019 Iranian Conference on Renewable Energy & Distributed Generation (ICREDG) - A Novel Method for Power Generation Using Trains

Garshasbi, Hamid, Mahmoudi, Abdullah

Year:

2019

File:

PDF, 929 KB

2019

23

A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian family

Masoud Garshasbi, Kimia Kahrizi, Masoumeh Hosseini, Leila Nouri Vahid, Masoumeh Falah, Sahel Hemmati, Hao Hu, Andreas Tzschach, Hans Hilger Ropers, Hossein Najmabadi, Andreas Walter Kuss

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 2.05 MB

english, 2011

24

Association of the dopamine transporter gene (DAT1) core promoter polymorphism −67T variant with schizophrenia

N. Khodayari, M. Garshasbi, F. Fadai, A. Rahimi, L. Hafizi, A. Ebrahimi, H. Najmabadi, Mina Ohadi

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 54 KB

english, 2004

25

Comparative investigation of the formation of polytetrafluoroethylene nanoparticles on different solid substrates through the adsorption of tetrafluoroethylene

Ashkan Garshasbi, Mohammad Mahdi Doroodmand, Reza Pooladi, Afsaneh Safavi, Mohammad Hossein Sheikhi

Journal:

Journal of Applied Polymer Science

Year:

2011

Language:

english

File:

PDF, 425 KB

english, 2011

26

Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1

Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, Kimia Kahrizi, Andreas Tzschach, Masoud Garshasbi, Hossein Najmabadi, Andreas Walter Kuss, Wolfram Kress, Geneviève Laureys, Bart Loeys, Eva Bri

Journal:

Year:

2009

Language:

english

File:

PDF, 1.09 MB

english, 2009

27

Numerical study of in-cylinder pressure in an internal combustion engine

A. Shidfar, M. Garshasbi

Journal:

Applied Mathematics and Computation

Year:

2005

Language:

english

File:

PDF, 271 KB

english, 2005

28

A numerical scheme for solving special class of nonlinear diffusion–convection equation

A. Shidfar, M. Djalalvand, M. Garshasbi

Journal:

Applied Mathematics and Computation

Year:

2005

Language:

english

File:

PDF, 273 KB

english, 2005

29

A computational procedure for estimation of an unknown coefficient in an inverse boundary value problem

M. Fakhraie, A. Shidfar, M. Garshasbi

Journal:

Applied Mathematics and Computation

Year:

2007

Language:

english

File:

PDF, 182 KB

english, 2007

30

A weighted algorithm based on Adomian decomposition method for solving an special class of evolution equations

A. Shidfar, M. Garshasbi

Journal:

Communications in Nonlinear Science and Numerical Simulation

Year:

2009

Language:

english

File:

PDF, 173 KB

english, 2009

31

Note on using radial basis functions and Tikhonov regularization method to solve an inverse heat conduction problem

A. Shidfar, Z. Darooghehgimofrad, M. Garshasbi

Journal:

Engineering Analysis with Boundary Elements

Year:

2009

Language:

english

File:

PDF, 165 KB

english, 2009

32

A method for solving an inverse biharmonic problem

A. Shidfar, A. Shahrezaee, M. Garshasbi

Journal:

Journal of Mathematical Analysis and Applications

Year:

2005

Language:

english

File:

PDF, 88 KB

english, 2005

33

SNP array-based homozygosity mapping revealsMCPH1deletion in family with autosomal recessive mental retardation and mild microcephaly

Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, Farkhondeh Behjati, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saghar Ghasemi Firouzabadi, Christian Becker, Franz Rüschendorf, Peter Nü

Journal:

Year:

2006

Language:

english

File:

PDF, 380 KB

english, 2006

34

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Hossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Wei Chen, Farkhondeh Behjati, Valeh Hadavi, Sahar Esmaeeli Nieh, Seyedeh Sedigheh Abedini, Reza Vazifeh

Journal:

Year:

2007

Language:

english

File:

PDF, 307 KB

english, 2007

35

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots

Andreas Walter Kuss, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Farkhondeh Behjati, Hossein Darvish, Lia Abbasi-Moheb, Lucia Puettmann, Agnes Zecha, Robert Weißmann, Hao Hu, Marzieh Mohseni, S

Journal:

Year:

2011

Language:

english

File:

PDF, 230 KB

english, 2011

36

A numerical procedure for estimation of the melt depth in laser material processing

A. Shidfar, M. Alinejadmofrad, M. Garshasbi

Journal:

Optics & Laser Technology

Year:

2009

Language:

english

File:

PDF, 301 KB

english, 2009

37

Alopecia–mental retardation syndrome: clinical and molecular characterization of four patients

A. Tzschach, B. Bozorgmehr, V. Hadavi, K. Kahrizi, M. Garshasbi, M.M. Motazacker, H.-H. Ropers, A.W. Kuss, H. Najmabadi

Journal:

British Journal of Dermatology

Year:

2008

Language:

english

File:

PDF, 355 KB

english, 2008

38

Cut-off value of 1-h, 50-g glucose challenge test for screening of gestational diabetes mellitus in an Iranian population

Samira Behboudi Gandevani, Ahia Garshasbi, Shiva Dibaj

Journal:

Journal of Obstetrics and Gynaecology Research

Year:

2011

Language:

english

File:

PDF, 296 KB

english, 2011

39

An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4

Kahrizi, Kimia, Najmabadi, Hossein, Kariminejad, Roxana, Jamali, Payman, Malekpour, Mahdi, Garshasbi, Masoud, Ropers, Hans Hilger, Kuss, Andreas Walter, Tzschach, Andreas

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 178 KB

english, 2008

40

Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3

Hu, Cougar Hao, Garshasbi, Masoud, Abedini, Seyedeh Sedigheh, Ghadami, Shirin, Kariminejad, Roxana, Ullmann, Reinhard, Chen, Wei, Ropers, H-Hilger, Kuss, Andreas W, Kahrizi, Kimia

Journal:

European Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 230 KB

english, 2010

41

Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome

Moheb, Lia Abbasi, Tzschach, Andreas, Garshasbi, Masoud, Kahrizi, Kimia, Darvish, Hossein, Heshmati, Yaser, Kordi, Alireza, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas Walter

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 108 KB

english, 2007

42

Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

Joanna Walczak-Sztulpa, Jonathan Eggenschwiler, Daniel Osborn, Desmond A. Brown, Francesco Emma, Claus Klingenberg, Raoul C. Hennekam, Giuliano Torre, Masoud Garshasbi, Andreas Tzschach, Malgorzata Sz

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.04 MB

english, 2010

43

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

Muhammad Arshad Rafiq, Andreas W. Kuss, Lucia Puettmann, Abdul Noor, Annapoorani Ramiah, Ghazanfar Ali, Hao Hu, Nadir Ali Kerio, Yong Xiang, Masoud Garshasbi, Muzammil Ahmad Khan, Gisele E. Ishak, Ros

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 860 KB

english, 2011

44

Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability

Muhammad Arshad Rafiq, Andreas W. Kuss, Lucia Puettmann, Abdul Noor, Annapoorani Ramiah, Ghazanfar Ali, Hao Hu, Nadir Ali Kerio, Yong Xiang, Masoud Garshasbi, Muzammil Ahmad Khan, Gisele E. Ishak, Ros

Journal:

The American Journal of Human Genetics

Year:

2011

File:

PDF, 25 KB

2011

45

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana Kariminejad, Farkhondeh Behjati, Andreas Tzschach, Hossein Najmabadi, Hans Hilger Ropers, Andreas Walter Kuss

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 1.14 MB

english, 2008

46

Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy

Sharareh Dadgar, Olivier Hagens, Seyed Razi Dadgar, Ehsan Nobakht Haghighi, Simone Schimpf, Bernd Wissinger, Masoud Garshasbi

Journal:

Experimental Eye Research

Year:

2006

Language:

english

File:

PDF, 381 KB

english, 2006

47

Beta-human chorionic gonadotropin in cervicovaginal secretions and preterm delivery

A. Garshasbi, T. Ghazanfari, S. Faghih Zadeh

Journal:

International Journal of Gynecology & Obstetrics

Year:

2004

Language:

english

File:

PDF, 205 KB

english, 2004

48

A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation

Mohammad Mahdi Motazacker, Benjamin Rainer Rost, Tim Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saeid Hosseini Amini, Chandan Goswami, And

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 6.13 MB

english, 2007

49

Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations

E Papari, M Bastami, A Farhadi, SS Abedini, M Hosseini, I Bahman, M Mohseni, M Garshasbi, L Abbasi Moheb, F Behjati, K Kahrizi, H-H Ropers, H Najmabadi

Journal:

Clinical Genetics

Year:

2012

Language:

english

File:

PDF, 610 KB

english, 2012

50

A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family

Püttmann, Lucia, Stehr, Henning, Garshasbi, Masoud, Hu, Hao, Kahrizi, Kimia, Lipkowitz, Bettina, Jamali, Payman, Tzschach, Andreas, Najmabadi, Hossein, Ropers, Hans-Hilger, Musante, Luciana, Kuss, And

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 326 KB

english, 2013

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@z-lib.do

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски