Kariminejad, A.: search on Z-Library

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

1

Gully erosion spatial modelling: Role of machine learning algorithms in selection of the best controlling factors and modelling process

Pourghasemi, Hamid Reza, Sadhasivam, Nitheshnirmal, Kariminejad, Narges, Collins, Adrian

Journal:

Geoscience Frontiers

Year:

2020

Language:

english

File:

PDF, 38.81 MB

english, 2020

2

Science of breeding and heredity from ancient Persia to modern Iran

Kariminejad, MohammadH, Khorshidian, Ardeshir

Journal:

Indian Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 173 KB

english, 2012

3

Effect of surface chemistry of graphene and its content on the properties of ethylene dichloride- and disodium tetrasulfide-based polysulfide polymer nanocomposites

Kariminejad, Bahareh, Salami-Kalajahi, Mehdi, Roghani-Mamaqani, Hossein, Noparvar-Qarebagh, Akbar

Journal:

Polymer Composites

Year:

2015

Language:

english

File:

PDF, 795 KB

english, 2015

4

How can statistical and artificial intelligence approaches predict piping erosion susceptibility?

Hosseinalizadeh, Mohsen, Kariminejad, Narges, Rahmati, Omid, Keesstra, Saskia, Alinejad, Mohammad, Mohammadian Behbahani, Ali

Journal:

Science of The Total Environment

Year:

2019

Language:

english

File:

PDF, 5.62 MB

english, 2019

5

GIS-Based Machine Learning Algorithms for Gully Erosion Susceptibility Mapping in a Semi-Arid Region of Iran

Lei, Xinxiang, Chen, Wei, Avand, Mohammadtaghi, Janizadeh, Saeid, Kariminejad, Narges, Shahabi, Hejar, Costache, Romulus, Shahabi, Himan, Shirzadi, Ataollah, Mosavi, Amir

Journal:

Year:

2020

File:

PDF, 4.58 MB

2020

6

Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome

Van Damme, Tim, Pang, Xiaomeng, Guillemyn, Brecht, Gulberti, Sandrine, Syx, Delfien, De Rycke, Riet, Kaye, Olivier, de Die-Smulders, Christine E M, Pfundt, Rolph, Kariminejad, Ariana, Nampoothiri, She

Journal:

Human Molecular Genetics

Year:

2018

Language:

english

File:

PDF, 339 KB

english, 2018

7

Optimizing linear alkyl benzene sulfonate removal using Fenton oxidation process in Taguchi Method

Khorsandi, H., Mohammadi, A., Kariminejad, F., Haghighi, M., Karimzadeh, S., Khorsandi, J., Aghapour, A. A.

Journal:

Journal of Water Chemistry and Technology

Year:

2016

Language:

english

File:

PDF, 434 KB

english, 2016

8

Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails

Kariminejad, Ariana, Ajeawung, Norbert Fonya, Bozorgmehr, Bita, Dionne-Laporte, Alexandre, Molidperee, Sirinart, Najafi, Kimia, Gibbs, Richard A, Lee, Brendan H, Hennekam, Raoul C, Campeau, Philippe M

Journal:

Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 654 KB

english, 2017

9

An assessment of metaheuristic approaches for flood assessment

Pourghasemi, Hamid Reza, Termeh, Seyed Vahid Razavi, Kariminejad, Narges, Hong, Haoyuan, Chen, Wei

Journal:

Journal of Hydrology

Year:

2020

File:

PDF, 5.86 MB

2020

10

Photodegradation of lignin from pulp and paper mill effluent using TiO2/PS composite under UV-LED radiation: Optimization, toxicity assessment and reusability study

Haghighi, Mohsen, Rahmani, Farhad, Kariminejad, Fatemeh, Sene, Rojiar Akbari

Journal:

Process Safety and Environmental Protection

Year:

2018

Language:

english

File:

PDF, 1.16 MB

english, 2018

11

A novel autosomal recessive GJB2 -associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss and palmoplantar keratoderma

Youssefian, Leila, Vahidnezhad, Hassan, Saeidian, Amir Hossein, Mahmoudi, Hamidreza, Karamzadeh, Razieh, Kariminejad, Ariana, Huang, Jianhe, Li, Leping, Jannace, Thomas F., Fortina, Paolo, Zeinali, Si

Journal:

Year:

2018

Language:

english

File:

PDF, 2.57 MB

english, 2018

12

An assessment of metaheuristic approaches for flood assessment

Pourghasemi, Hamid Reza, Termeh, Seyed Vahid Razavi, Kariminejad, Narges, Hong, Haoyuan, Chen, Wei

Journal:

Journal of Hydrology

Year:

2020

Language:

english

File:

PDF, 5.86 MB

english, 2020

13

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization

Behjati, Farkhondeh, Firouzabadi, SagharGhasemi, Ghasemlou, BehruzEbrahimizade, Jamali, Peyman, Bahman, Ideh, Kariminejad, Roxana, Vameghi, Roshanak, Sajedi, Firouzeh, Shafaghati, Yousef, Shojaei, Aza

Journal:

Indian Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 555 KB

english, 2013

14

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

Marianne Rohrbach, Anthony Vandersteen, Uluç Yiş, Gul Serdaroglu, Esra Ataman, Maya Chopra, Sixto Garcia, Kristi Jones, Ariana Kariminejad, Marius Kraenzlin, Carlo Marcelis, Matthias Baumgartner, Ceci

Journal:

Orphanet Journal of Rare Diseases

Year:

2011

Language:

english

File:

PDF, 598 KB

english, 2011

15

159 PASH syndrome is not a genetically distinct entity but belongs to the spectrum of autoinflammatory skin phenotypes

Uitto, J., Faraji Zonooz, M., Sabbagh-Kermani, F., Fattahi, Z., Fadaee, M., Reza Akbari, M., Amiri, R., Vahidnezhad, H., Najmabadi, H., Kariminejad, A.

Journal:

The Journal of Investigative Dermatology

Year:

2016

Language:

english

File:

PDF, 55 KB

english, 2016

16

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Todd, Emily J., Yau, Kyle S., Ong, Royston, Slee, Jennie, McGillivray, George, Barnett, Christopher P., Haliloglu, Goknur, Talim, Beril, Akcoren, Zuhal, Kariminejad, Ariana, Cairns, Anita, Clarke, Nig

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 2.09 MB

english, 2015

17

SLC2A2mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion

Sansbury, F. H., Flanagan, S. E., Houghton, J. A. L., Shuixian Shen, F. L., Al-Senani, A. M. S., Habeb, A. M., Abdullah, M., Kariminejad, A., Ellard, S., Hattersley, A. T.

Journal:

Year:

2012

Language:

english

File:

PDF, 120 KB

english, 2012

18

Indoor Air Quality associations with sick building syndrome: An application of decision tree technology

Sarkhosh, Maryam, Najafpoor, Ali Asghar, Alidadi, Hosein, Shamsara, Jamal, Amiri, Hanieh, Andrea, Tittarelli, Kariminejad, Fatemeh

Journal:

Building and Environment

Year:

2020

File:

PDF, 1.22 MB

2020

19

Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum

Kariminejad, Ariana, Ghaderi-Sohi, Siavash, Hossein-Nejad Nedai, Hamid, Varasteh, Vahid, Moslemi, Ali-Reza, Tajsharghi, Homa

Journal:

BMC Musculoskeletal Disorders

Year:

2016

Language:

english

File:

PDF, 894 KB

english, 2016

20

Nanohybrids of novolac phenolic resin and carbon nanotube-containing silica network

Noparvar-Qarebagh, Akbar, Roghani-Mamaqani, Hossein, Salami-Kalajahi, Mehdi, Kariminejad, Bahareh

Journal:

Journal of Thermal Analysis and Calorimetry

Year:

2017

Language:

english

File:

PDF, 2.18 MB

english, 2017

21

Amelia, cleft lip, and holoprosencephaly: A distinct entity

Ariana Kariminejad, Payman Goodarzi, Alaleh Asghari-Roodsari, Mohamad Hasan Kariminejad

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 98 KB

english, 2009

22

Skull defects, alopecia, hypertelorism, and notched alae nasi caused by homozygous ALX4 gene mutation

Kariminejad, Ariana, Bozorgmehr, Bita, Alizadeh, Houman, Ghaderi-Sohi, Siavash, Toksoy, Güven, Uyguner, Zehra Oya, Kayserili, Hülya

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 1.38 MB

english, 2014

23

Complete COL1A1 allele deletions in osteogenesis imperfecta

van Dijk, Fleur S, Huizer, Margriet, Kariminejad, Ariana, Marcelis, Carlo L, Plomp, Astrid S, Terhal, Paulien A, Meijers-Heijboer, Hanne, Weiss, Marjan M, van Rijn, Rick R, Cobben, Jan M, Pals, Gerard

Journal:

Genetics in Medicine

Year:

2010

Language:

english

File:

PDF, 660 KB

english, 2010

24

TOR1A variants cause a severe arthrogryposis with developmental delay, strabismus and tremor

Kariminejad, A., Dahl-Halvarsson, M., Ravenscroft, G., Afroozan, F., Keshavarz, E., Goullée, H., Davis, M., Laing, N., Tajsharghi, H.

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 238 KB

english, 2017

25

Assessing and mapping multi-hazard risk susceptibility using a machine learning technique

Pourghasemi, Hamid Reza, Kariminejad, Narges, Amiri, Mahdis, Edalat, Mohsen, Zarafshar, Mehrdad, Blaschke, Thomas, Cerda, Artemio

Journal:

Scientific Reports

Year:

2020

Language:

english

File:

PDF, 4.59 MB

english, 2020

26

Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders

Abdelfattah, Fatima, Kariminejad, Ariana, Kahlert, AnneâKarin, Morrison, Patrick J., Gumus, Evren, Mathews, Katherine D., Darbro, Benjamin W., Amor, David J., Walsh, Maie, Sznajer, Yves, WeiÃ, Luis

Journal:

Year:

2020

File:

PDF, 453 KB

2020

27

Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran

Najmabadi, Hossein, Ghamari, Alireza, Sahebjam, Farhad, Kariminejad, Roxana, Hadavi, Valeh, Khatibi, Talayeh, Samavat, Ashraf, Mehdipour, Elaheh, Modell, Bernadette, Kariminejad, Mohammand Hassan

Journal:

Community Genetics

Year:

2006

Language:

english

File:

PDF, 115 KB

english, 2006

28

Mutations in GRIP1 cause Fraser syndrome

Vogel, M. J., van Zon, P., Brueton, L., Gijzen, M., van Tuil, M. C., Cox, P., Schanze, D., Kariminejad, A., Ghaderi-Sohi, S., Blair, E., Zenker, M., Scambler, P. J., Ploos van Amstel, H. K., van Haels

Journal:

Journal of Medical Genetics

Year:

2012

Language:

english

File:

PDF, 452 KB

english, 2012

29

[Society of Petroleum Engineers SPE/ICoTA Coiled Tubing and Well Intervention Conference and Exhibition - The Woodlands, Texas, USA (2018-03-20)] SPE/ICoTA Coiled Tubing and Well Intervention Conference and Exhibition - Coiled Tubing Drilling: Case Study, New Zealand

Kariminejad, Soheil, Lundin, Henrik, Horvath, Lucas, Sweet, Steven

Language:

english

File:

PDF, 1.83 MB

english

30

Whole Genome Linkage Analysis Followed by Whole Exome Sequencing Identifies Nicastrin (NCSTN) as a Causative Gene in a Multiplex Family with γ-Secretase Spectrum of Autoinflammatory Skin Phenotypes

Faraji Zonooz, Mehrshid, Sabbagh-Kermani, Farahnaz, Fattahi, Zohreh, Fadaee, Mahsa, Akbari, Mohammad Reza, Amiri, Rezvan, Vahidnezhad, Hassan, Uitto, Jouni, Najmabadi, Hossein, Kariminejad, Ariana

Journal:

The Journal of Investigative Dermatology

Year:

2016

Language:

english

File:

PDF, 1.17 MB

english, 2016

31

Juvenile nephronophthisis and dysthyroidism: a rare association

Amiri, Fateme Shamekhi, Kariminejad, Ariana

Journal:

CEN Case Reports

Year:

2017

Language:

english

File:

PDF, 825 KB

english, 2017

32

De-novo interstitial 2.33 Mb deletion in 8q24.3

Akbaroghli, Susan, Tonekaboni, Seyed H., Kariminejad, Roxana, Liehr, Thomas, Coci, Emanuele G.

Journal:

Clinical Dysmorphology

Year:

2018

Language:

english

File:

PDF, 154 KB

english, 2018

33

Widespread aplasia cutis congenita in sibs with PLEC1 and ITGB4 variants

Kariminejad, Ariana, Vahidnezhad, Hassan, Ghaderi‐Sohi, Siavash, Ghannadan, Ali R., Youssefian, Leila, Parsimehr, Elham, Faraji Zonooz, Mehrshid, Kariminejad, Mohammad H., Uitto, Jouni, Najmabadi, Hos

Journal:

American Journal of Medical Genetics Part A

Year:

2019

Language:

english

File:

PDF, 2.78 MB

english, 2019

34

Clinical variability in acro-cardio-facial-syndrome

Ariana Kariminejad, Bita Bozorgmehr, Mohammad Ali Sedighi Gilani, Navid Almadani, Mohamad Hasan Kariminejad

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 95 KB

english, 2008

35

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

36

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

37

Increased Endoplasmic Reticulum Stress in patients with Congenital Liver Fibrosis caused by germline mutations in a Protein Disulfide Isomerase

Chia, Poh Hui, Kariminejad, Ariana, Rump, Patrick, Reversade, Bruno

Journal:

Mechanisms of Development

Year:

2017

Language:

english

File:

PDF, 46 KB

english, 2017

38

Evaluation of COD, color and lignin removal from pulp and paper effluent by anaerobic sludge biosorption

Kariminejad, Fatemeh, Yousefi, Zabihollah, Cherati, Jamshid Yazdani

Journal:

International Journal of Environmental Science and Technology

Year:

2017

Language:

english

File:

PDF, 1.37 MB

english, 2017

39

A GLI3 variant leading to polydactyly in heterozygotes and PallisterâHallâlike syndrome in a homozygote

Kariminejad, Ariana, GhaderiâSohi, Siavash, Keshavarz, Elham, Hashemi, Seyed Abolghasem, Parsimehr, Elham, SzenkerâRavi, Emmanuelle, Khatoo, Muznah, Faraji Zonooz, Mehrshid, Reversade, Bruno, Najm

Journal:

Clinical Genetics

Year:

2020

File:

PDF, 2.47 MB

2020

40

Defect in proline synthesis: pyrroline-5-carboxylate reductase 1 deficiency leads to a complex clinical phenotype with collagen and elastin abnormalities

Rita Kretz, Bita Bozorgmehr, Mohamad Hasan Kariminejad, Marianne Rohrbach, Ingrid Hausser, Alessandra Baumer, Matthias Baumgartner, Cecilia Giunta, Ariana Kariminejad, Johannes Häberle

Journal:

Journal of Inherited Metabolic Disease

Year:

2011

Language:

english

File:

PDF, 548 KB

english, 2011

41

Aphonia, microstomia, deafness, retinal dystrophy, duplicated halluces and intellectual disability

Ariana Kariminejad, Raoul C.M. Hennekam

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 297 KB

english, 2012

42

Mutations in MAB21L2 Result in Ocular Coloboma, Microcornea and Cataracts

Deml, Brett, Kariminejad, Ariana, Borujerdi, Razieh H. R., Muheisen, Sanaa, Reis, Linda M., Semina, Elena V., Barsh, Gregory S.

Journal:

Year:

2015

Language:

english

File:

PDF, 15.84 MB

english, 2015

43

Report of limb girdle muscular dystrophy type 2A in 6 iranian patients, one with a novel deletion in CAPN3 gene

Fadaee, Mahsa, Kariminejad, Ariana, Fattahi, Zohreh, Nafissi, Shahriar, Godarzi, Hamed Reza, Beheshtian, Maryam, Vazehan, Raheleh, Akbari, Mohammad Reza, Kahrizi, Kimia, Najmabadi, Hossein

Journal:

Neuromuscular Disorders

Year:

2016

Language:

english

File:

PDF, 886 KB

english, 2016

44

Lethal multiple pterygium syndrome associated with mutations in the type 1 ryanodine receptor (RYR1)

Kariminejad, A., Ghaderi-Sohi, S., Hossein-Nejad Nedai, H., Varasteh, V., Tajsharghi, H.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 208 KB

english, 2015

45

Mutation analysis of the STRA6 gene in isolated and non-isolated anophthalmia/microphthalmia

N Chassaing, N Ragge, A Kariminejad, A Buffet, S Ghaderi-Sohi, J Martinovic, P Calvas

Journal:

Clinical Genetics

Year:

2012

Language:

english

File:

PDF, 677 KB

english, 2012

46

Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings

Shojaei, Azadeh, Behjati, Farkhondeh, Derakhshandeh-Peykar, Pupak, Razzaghy-Azar, Maryam, Otukesh, Hasan, Kariminejad, Roxana, Dowlati, Mohammad-Ali, Rashidi-Nezhad, Ali, Tavakkoly-Bazzaz, Javad

Journal:

Year:

2013

Language:

english

File:

PDF, 590 KB

english, 2013

47

HUMAN TESTOSTERONE-OESTRADIOL BINDING GLOBULIN IN HEALTH AND DISEASE

WENN, R. V., KAMBERI, I. A., VOSSOUGH, P., KARIMINEJAD, M. H., TORABEE, E., AYOUGHI, F., KEYVANJAH, M., SARBERI, N.

Journal:

Obstetric and Gynecologic Survey

Year:

1977

File:

PDF, 187 KB

1977

48

The effect of nano-SiO 2 on the physicochemical and structural properties of gelatin-polyvinyl alcohol composite films

Kariminejad, Mohaddeseh, Sadeghi, Ehsan, Rouhi, Milad, Mohammadi, Reza, Askari, Fatemeh, Taghizadeh, Masoumeh, Moradi, Shirin

Journal:

Journal of Food Process Engineering

Year:

2018

File:

PDF, 638 KB

2018

49

Homozygous deletion of the entire AAAS gene in a triple A syndrome patient

Koehler, Katrin, Hackmann, Karl, Landgraf, Dana, Schubert, Tina, Shakiba, Marjan, Kariminejad, Ariana, Huebner, Angela

Journal:

European Journal of Medical Genetics

Year:

2019

File:

PDF, 8.92 MB

2019

50

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana

Journal:

Clinical Case Reports

Year:

2019

Language:

english

File:

PDF, 583 KB

english, 2019

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@1delivery.pm

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