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1

Investigating Asymmetric Effects of Monetary Shocks on the Exchange Rate and Trade Balance, with an Emphasis on Inflation Targeting

Elahi, Naser, Salimi, Farshid, Masoomzadeh, Elahe

Journal:

Procedia Economics and Finance

Year:

2016

Language:

english

File:

PDF, 315 KB

english, 2016

2

Kavosh: a new algorithm for finding network motifs

Zahra Razaghi Moghadam Kashani, Hayedeh Ahrabian, Elahe Elahi, Abbas Nowzari-Dalini, Elnaz Saberi Ansari, Sahar Asadi, Shahin Mohammadi, Falk Schreiber, Ali Masoudi-Nejad

Journal:

BMC Bioinformatics

Year:

2009

Language:

english

File:

PDF, 1.17 MB

english, 2009

3

Discovery of single nucleotide polymorphisms and mutations by Pyrosequencing

Mostafa Ronaghi, Elahe Elahi

Journal:

Comparative and Functional Genomics

Year:

2002

Language:

english

File:

PDF, 196 KB

english, 2002

4

A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients

Seyedmehdi Shojaee, Farzad Sina, Niloofar Farboodi, Zeinab Fazlali, Farzaneh Ghazavi, Seyed Ali Ghorashi, Khosro Parsa, Homa Sadeghi, Gholam-Ali Shahidi, Mostafa Ronaghi, Elahe Elahi

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 81 KB

english, 2009

5

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

Coro Paisán-Ruiz, Rocio Guevara, Monica Federoff, Hasmet Hanagasi, Fardaz Sina, Elahe Elahi, Susanne A. Schneider, Petra Schwingenschuh, Nin Bajaj, Murat Emre, Andrew B. Singleton, John Hardy, Kailash

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 359 KB

english, 2010

6

Pyrosequencing for microbial typing

Mostafa Ronaghi, Elahe Elahi

Journal:

Journal of Chromatography B

Year:

2002

Language:

english

File:

PDF, 242 KB

english, 2002

7

Intragenic SNP haplotypes associated with 84dup18 mutation inTNFRSF11Ain four FEO pedigrees suggest three independent origins for this mutation

Elahe Elahi, Yousef Shafaghati, Sareh Asadi, Farnaz Absalan, Hani Goodarzi, Nava Gharaii, Mohammad Hassan Karimi-Nejad, Farhad Shahram, Anne E. Hughes

Journal:

Journal of Bone and Mineral Metabolism

Year:

2007

Language:

english

File:

PDF, 300 KB

english, 2007

8

Homozygous Missense Mutation in Fibulin-5 in an Iranian Autosomal Recessive Cutis Laxa Pedigree and Associated Haplotype

Elahi, Elahe, Kalhor, Reza, Banihosseini, Setareh S, Torabi, Noorossadat, Pour-Jafari, Hamid, Houshmand, Massoud, Amini, Seyed S H, Ramezani, Ahmad, Loeys, Bart

Journal:

The Journal of Investigative Dermatology

Year:

2006

Language:

english

File:

PDF, 84 KB

english, 2006

9

Neural differentiation of mouse embryonic stem cells on conductive nanofiber scaffolds

Mahboubeh Kabiri, Masoud Soleimani, Iman Shabani, Kathryn Futrega, Naser Ghaemi, Hana Hanaee Ahvaz, Elahe Elahi, Michael R. Doran

Journal:

Biotechnology Letters

Year:

2012

Language:

english

File:

PDF, 486 KB

english, 2012

10

Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP Arrays

Seyedmehdi Shojaee, Farzad Sina, Setareh Sadat Banihosseini, Mohammad Hossein Kazemi, Reza Kalhor, Gholam-Ali Shahidi, Hossein Fakhrai-Rad, Mostafa Ronaghi, Elahe Elahi

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 618 KB

english, 2008

11

Determination of hepatitis C virus genotype by Pyrosequencing

Elahe Elahi, Nader Pourmand, Ramsey Chaung, Ara Rofoogaran, Judie Boisver, Katayon Samimi-Rad, Ronald W. Davis, Mostafa Ronaghi

Journal:

Journal of Virological Methods

Year:

2003

Language:

english

File:

PDF, 400 KB

english, 2003

12

Manifestation of diffuse yellowish keratoderma on the palms and soles in autosomal recessive congenital ichthyosis patients may be indicative of mutations in NIPAL4

Afagh ALAVI, Mostafa M. SHAHSHAHANI, Brandy KLOTZLE, Jian-Bing FAN, Mostafa RONAGHI, Elahe ELAHI

Journal:

The Journal of Dermatology

Year:

2012

Language:

english

File:

PDF, 382 KB

english, 2012

13

Global haplotype partitioning for maximal associated SNP pairs

Ali Katanforoush, Mehdi Sadeghi, Hamid Pezeshk, Elahe Elahi

Journal:

BMC Bioinformatics

Year:

2009

Language:

english

File:

PDF, 489 KB

english, 2009

14

Mutation screening of TGFBI in two Iranian Avellino corneal dystrophy pedigrees

Afagh Alavi, Elahe Elahi, Mohsen Rahmati-Kamel, Farid Karimian, Mojgan Rezaei-Kanavi

Journal:

Clinical & Experimental Ophthalmology

Year:

2008

Language:

english

File:

PDF, 305 KB

english, 2008

15

Variable Expressivity and High Penetrance of CYP1B1 Mutations Associated with Primary Congenital Glaucoma

Fatemeh Suri, Shahin Yazdani, Mehrnaz Narooie-Nejhad, Seyed Jalal Zargar, Seyed Hassan Paylakhi, Sirous Zeinali, Mohammad Pakravan, Elahe Elahi

Journal:

Year:

2009

Language:

english

File:

PDF, 1.50 MB

english, 2009

16

Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients

Seyedmehdi Shojaee, Zeinab Fazlali, Farzaneh Ghazavi, Setareh Sadat Banihosseini, Mohammad Hossein Kazemi, Khosro Parsa, Homa Sadeghi, Farzad Sina, Gholam-Ali Shahidi, Mostafa Ronaghi, Elahe Elahi

Journal:

Neuroscience Letters

Year:

2009

Language:

english

File:

PDF, 222 KB

english, 2009

17

Cytochrome c oxidase subunit 1 barcode data of fish of the Nayband National Park in the Persian Gulf and analysis using meta-data flag several cryptic species

HOSSEINALI ASGHARIAN, HOMAYOUN HOSSEINZADEH SAHAFI, ARIA ASHJA ARDALAN, SHAHROKH SHEKARRIZ, ELAHE ELAHI

Journal:

Molecular Ecology Resources

Year:

2011

Language:

english

File:

PDF, 697 KB

english, 2011

18

Concentrations of nitric oxide metabolites in the serum of Iranian multiple sclerosis patients

Mehrzad Roghani, Fereidoun Mahboudi, Mohammad Ali Saharian, Masoud Etemadifar, Ali Naji Esfahani, Hossein Nahrevanian, Elahe Elahi

Journal:

Journal of the Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 197 KB

english, 2010

19

PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation

Dezfouli, Mitra Ansari, Alavi, Afagh, Rohani, Mohammad, Rezvani, Mohamad, Nekuie, Tayebeh, Klotzle, Brandy, Tonekaboni, Seyed Hasan, Shahidi, Gholam Ali, Elahi, Elahe

Journal:

Movement Disorders

Year:

2013

Language:

english

File:

PDF, 212 KB

english, 2013

20

Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients

Dezfouli, Mitra Ansari, Yadegari, Samira, Nafissi, Shahriar, Elahi, Elahe

Journal:

Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 322 KB

english, 2012

21

Normalization of miRNA qPCR high-throughput data: a comparison of methods

Mohammadian, Ali, Mowla, Seyed Javad, Elahi, Elahe, Tavallaei, Mahmood, Nourani, Mohammad Reza, Liang, Yu

Journal:

Biotechnology Letters

Year:

2013

Language:

english

File:

PDF, 670 KB

english, 2013

22

CYP1B1 Mutation Profile of Iranian Primary Congenital Glaucoma Patients and Associated Haplotypes

Chitsazian, Fereshteh, Tusi, Betsabeh Khoramian, Elahi, Elahe, Saroei, Heidar Amini, Sanati, Mohammad H., Yazdani, Shahin, Pakravan, Mohammad, Nilforooshan, Navid, Eslami, Yadollah, Mehrjerdi, Mohamma

Journal:

The Journal of Molecular Diagnostics

Year:

2007

Language:

english

File:

PDF, 307 KB

english, 2007

23

Mutation in CYP27A1 identified in family with coronary artery disease

InanlooRahatloo, Kolsoum, Zand Parsa, Amir Farhang, Huse, Klaus, Rasooli, Paniz, Davaran, Saeid, Platzer, Matthias, Fan, Jian-Bing, Amini, Sasan, Steemers, Frank, Elahi, Elahe

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 704 KB

english, 2013

24

Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients

Alavi, Afagh, Nafissi, Shahriar, Rohani, Mohammad, Shahidi, Gholamali, Zamani, Babak, Shamshiri, Hosein, Safari, Iman, Elahi, Elahe

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 991 KB

english, 2014

25

Identification of mutation in NPC2 by exome sequencing results in diagnosis of Niemann–Pick disease type C

Alavi, Afagh, Nafissi, Shahriar, Shamshiri, Hosein, Nejad, Maryam Malakooti, Elahi, Elahe

Journal:

Molecular Genetics and Metabolism

Year:

2013

Language:

english

File:

PDF, 853 KB

english, 2013

26

Meeting announcement

Alavi, Afagh, Nafissi, Shahriar, Shamshiri, Hosein, Nejad, Maryam Malakooti, Elahi, Elahe

Journal:

Year:

1980

File:

PDF, 32 KB

1980

27

Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients

Alavi, Afagh, Nafissi, Shahriar, Rohani, Mohammad, Zamani, Babak, Sedighi, Behnaz, Shamshiri, Hosein, Fan, Jian-Bing, Ronaghi, Mostafa, Elahi, Elahe

Journal:

Neurobiology of Aging

Year:

2013

Language:

english

File:

PDF, 318 KB

english, 2013

28

A Haplotype Framework for Cystic Fibrosis Mutations in Iran

Elahi, Elahe, Khodadad, Ahmad, Kupershmidt, Ilya, Ghasemi, Fereshteh, Alinasab, Babak, Naghizadeh, Ramin, Eason, Robert G., Amini, Mahshid, Esmaili, Mehran, Esmaeili Dooki, Mohammad R., Sanati, Mohamm

Journal:

The Journal of Molecular Diagnostics

Year:

2006

Language:

english

File:

PDF, 144 KB

english, 2006

29

Identification of p.Gln858* in ATP13A2 in two EOPD patients and presentation of their clinical features

Malakouti-Nejad, Maryam, Shahidi, Gholam-Ali, Rohani, Mohammad, Shojaee, Seyed Mehdi, Hashemi, Mehrdad, Klotzle, Brandy, Fan, Jian-Bing, Elahi, Elahe

Journal:

Neuroscience Letters

Year:

2014

Language:

english

File:

PDF, 1.31 MB

english, 2014

30

The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine

Jaberi, Elham, Chitsazian, Fereshteh, Ali Shahidi, Gholam, Rohani, Mohammad, Sina, Farzad, Safari, Iman, Malakouti Nejad, Maryam, Houshmand, Masoud, Klotzle, Brandy, Elahi, Elahe

Journal:

Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 1.17 MB

english, 2013

31

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis

Suri, Fatemeh, Narooie-Nejad, Mehrnaz, Safari, Iman, Moazzeni, Hamidreza, Rohani, Mohammad-Reza, Khajeh, Ali, Klotzle, Brandy, Fan, Jian-Bing, Elahi, Elahe

Journal:

Journal of the Neurological Sciences

Year:

2014

Language:

english

File:

PDF, 563 KB

english, 2014

32

Effects of ribosomal wash factors and spermidine on endogenous and exogenous mRNA stimulated protein synthesis in the wheat germ cell-free system

Elahi, Elahe, Jones, George H.

Journal:

Canadian Journal of Biochemistry

Year:

1979

Language:

english

File:

PDF, 736 KB

english, 1979

33

HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry

Alavi, Afagh, Shamshiri, Hosein, Nafissi, Shahriar, Khani, Marzieh, Klotzle, Brandy, Fan, Jian-Bing, Steemers, Frank, Elahi, Elahe

Journal:

Neurobiology of Aging

Year:

2015

Language:

english

File:

PDF, 932 KB

english, 2015

34

Phylogenetic relationships of Mesobuthus eupeus (C.L. Koch, 1839) inferred from COI sequences (Scorpiones: Buthidae)

Mirshamsi, Omid, Sari, Alireza, Elahi, Elahe, Hosseinie, Shidokht

Journal:

Journal of Natural History

Year:

2010

Language:

english

File:

PDF, 1.58 MB

english, 2010

35

The p.Gly61Glu Mutation in CYP1B1 Affects the Extracellular Matrix in Glaucoma Patients

Safari, Iman, Suri, Fatemeh, Haji-Seyed-Javadi, Ramona, Yazdani, Shahin, Elahi, Elahe

Journal:

Ophthalmic Research

Year:

2016

Language:

english

File:

PDF, 876 KB

english, 2016

36

Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients

Yazdani, Shahin, Miraftabi, Arezoo, Pakravan, Mohammad, Ghahari, Elham, Tousi, Betsabeh K., Sedigh, Massih, Yaseri, Mehdi, Elahi, Elahe

Journal:

Journal of Glaucoma

Year:

2016

Language:

english

File:

PDF, 155 KB

english, 2016

37

Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2

Moazzeni, Hamidreza, Akbari, Mohammad Taghi, Yazdani, Shahin, Elahi, Elahe

Journal:

Year:

2016

Language:

english

File:

PDF, 832 KB

english, 2016

38

Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations

Khani, Marzieh, Shamshiri, Hosein, Alavi, Afagh, Nafissi, Shahriar, Elahi, Elahe

Journal:

Journal of the Neurological Sciences

Year:

2016

Language:

english

File:

PDF, 560 KB

english, 2016

39

Mutations in C19orf12 and intronic repeat expansions in C9orf72 not observed in Iranian Parkinson's disease patients

Alavi, Afagh, Malakouti Nejad, Maryam, Shahidi, Gholamali, Elahi, Elahe

Journal:

Neurobiology of Aging

Year:

2017

Language:

english

File:

PDF, 292 KB

english, 2017

40

PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability

Journal:

Movement Disorders

Year:

2017

Language:

english

File:

PDF, 87 KB

english, 2017

41

LTBP2 knockdown and oxidative stress affect glaucoma features including TGFβ pathways, ECM genes expression and apoptosis in trabecular meshwork cells

Suri, Fatemeh, Yazdani, Shahin, Elahi, Elahe

Journal:

Year:

2018

Language:

english

File:

PDF, 4.65 MB

english, 2018

42

Four Mutations (Three Novel, One Founder) in TACSTD2 among Iranian GDLD Patients

Alavi, Afagh, Elahi, Elahe, Tehrani, Mehdi Hosseini, Amoli, Fahimeh Asadi, Javadi, Mohammad-Ali, Rafati, Nasrin, Chiani, Mohsen, Banihosseini, Setareh Sadat, Bayat, Behnaz, Kalhor, Reza, Amini, Seyed

Journal:

Investigative Ophthalmology & Visual Science

Year:

2007

Language:

english

File:

PDF, 384 KB

english, 2007

43

Review of the earthworm fauna of Iran with emphasis on Kohgiluyeh & Boyer-Ahmad Province

FARHADI, ZEINAB, MALEK, MASOUMEH, ELAHI, ELAHE

Journal:

Year:

2013

Language:

english

File:

PDF, 1.52 MB

english, 2013

44

Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients

Khani, Marzieh, Alavi, Afagh, Shamshiri, Hosein, Zamani, Babak, Hassanpour, Hosein, Kazemi, Mohammad Hossein, Nafissi, Shahriar, Elahi, Elahe

Journal:

Neurobiology of Aging

Year:

2018

Language:

english

File:

PDF, 392 KB

english, 2018

45

Comparing the Effect of Schema-Based Education and Social Problem Solving Training on Social Competence and Expressions of Identity in Adolescents

Elahi, Elahe, Sepahmansour, Mojgan, Golshani, Fatemeh, Emamipour, Susan

Journal:

Mediterranean Journal of Social Sciences

Year:

2016

Language:

english

File:

PDF, 205 KB

english, 2016

46

CYP4V2 mutation screening in an Iranian Bietti crystalline dystrophy pedigree and evidence for clustering of CYP4V2 mutations

Darki, Faezeh, Fekri, Sahba, Farhangmehr, Shaghayegh, Ahmadieh, Hamid, Dehghan, Mohammad Hossein, Elahi, Elahe

Journal:

Journal of Current Ophthalmology

Year:

2019

Language:

english

File:

PDF, 1.78 MB

english, 2019

47

Screening for MIR184 mutations in Iranian patients with keratoconus

Farzadfard, Azad, Nassiri, Nader, Moghadam, TayebehNekuie, Paylakhi, SeyedHassan, Elahi, Elahe

Journal:

Journal of Ophthalmic and Vision Research

Year:

2016

Language:

english

File:

PDF, 507 KB

english, 2016

48

Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies

Moazzeni, Hamidreza, Mirrahimi, Mehraban, Moghadam, Abolfazl, Banaei-Esfahani, Amir, Yazdani, Shahin, Elahi, Elahe

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 1.66 MB

english, 2019

49

Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies

Moazzeni, Hamidreza, Mirrahimi, Mehraban, Moghadam, Abolfazl, Banaei-Esfahani, Amir, Yazdani, Shahin, Elahi, Elahe

Journal:

Human Molecular Genetics

Year:

2019

File:

PDF, 1.66 MB

2019

50

Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree

Alavi, Afagh, Darki, Faezeh, Bidgoli, Mohammad Masoud Rahimi, Zare-Abdollahi, Davood, Moini, Ashraf, Shahshahani, Mostafa M., Fischer, Judith, Elahi, Elahe

Journal:

Molecular Genetics and Genomics

Year:

2020

File:

PDF, 1.42 MB

2020