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Financial Literacy of New Job Entrants.
Published in:
Pertanika Journal of Social Sciences & Humanities, 2013, v. 21, n. 2, p. 713
By:
- Kaur, Anupriya;
- Mittal, Niti;
- Agarwal, Sanchita
Publication type:
Article
Future Technocrats Perception on Dissemination of Technology.
Published in:
Pertanika Journal of Social Sciences & Humanities, 2013, v. 21, n. 1, p. 361
By:
- Kaur, Anupriya;
- Kaushal, Madhur;
- Sisodia, Jai;
- Chopra, Shruti
Publication type:
Article
Indian Youth Inclination towards Unethical Practices in the use of Information and Communication Technology.
Published in:
Pertanika Journal of Social Sciences & Humanities, 2012, v. 20, n. 4, p. 1311
By:
- Goel, Niket;
- Kaur, Anupriya;
- Vaidya, Meghna
Publication type:
Article
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation.
Published in:
BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0759-1
By:
- Sheth, Jayesh;
- Bhavsar, Riddhi;
- Mistri, Mehul;
- Pancholi, Dhairya;
- Bavdekar, Ashish;
- Dalal, Ashwin;
- Ranganath, Prajnya;
- Girisha, Katta M;
- Shukla, Anju;
- Phadke, Shubha;
- Puri, Ratna;
- Panigrahi, Inusha;
- Kaur, Anupriya;
- Muranjan, Mamta;
- Goyal, Manisha;
- Ramadevi, Radha;
- Shah, Raju;
- Nampoothiri, Sheela;
- Danda, Sumita;
- Datar, Chaitanya
Publication type:
Article
Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease.
Published in:
Molecular Biology Reports, 2022, v. 49, n. 8, p. 7399, doi. 10.1007/s11033-022-07533-8
By:
- Singh, Ankita;
- Rawat, Amit;
- Kaur, Anit;
- Kaur, Anupriya;
- Kumrah, Rajni;
- Johnson, Nameirakpam;
- Chaudhary, Himanshi;
- Pilania, Rakesh Kumar;
- Srivastava, Priyanka;
- Singh, Surjit
Publication type:
Article
Landscape of genetic infantile epileptic spasms syndrome—A multicenter cohort of 124 children from India.
Published in:
Epilepsia Open, 2023, v. 8, n. 4, p. 1383, doi. 10.1002/epi4.12811
By:
- Nagarajan, Balamurugan;
- Gowda, Vykuntaraju K.;
- Yoganathan, Sangeetha;
- Sharawat, Indar Kumar;
- Srivastava, Kavita;
- Vora, Nitish;
- Badheka, Rahul;
- Danda, Sumita;
- Kalane, Umesh;
- Kaur, Anupriya;
- Madaan, Priyanka;
- Mehta, Sanjiv;
- Negi, Sandeep;
- Panda, Prateek Kumar;
- Rajadhyaksha, Surekha;
- Saini, Arushi Gahlot;
- Saini, Lokesh;
- Shah, Siddharth;
- Srinivasan, Varunvenkat M.;
- Suthar, Renu
Publication type:
Article
Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndrome.
Published in:
Clinical Genetics, 2019, v. 95, n. 3, p. 398, doi. 10.1111/cge.13468
By:
- Somashekar, Puneeth H.;
- Girisha, Katta M.;
- Shukla, Anju;
- Lewis, Leslie E. S.;
- Shailaja, Shenoy;
- Nampoothiri, Sheela;
- Gowrishankar, Kalpana;
- Devi, Radha R.;
- Gupta, Neerja;
- Narayanan, Dhanya L.;
- Kaur, Anupriya;
- Bajaj, Shruti;
- Jagadeesh, Sujatha
Publication type:
Article
Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.
Published in:
Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03300-z
By:
- Sheth, Jayesh;
- Nair, Aadhira;
- Sheth, Frenny;
- Ajagekar, Manali;
- Dhondekar, Tejasvi;
- Panigrahi, Inusha;
- Bavdekar, Ashish;
- Nampoothiri, Sheela;
- Datar, Chaitanya;
- Gandhi, Ajit;
- Muranjan, Mamta;
- Kaur, Anupriya;
- Desai, Manisha;
- Mistri, Mehul;
- Patel, Chitra;
- Naik, Premal;
- Shah, Maulin;
- Godbole, Koumudi;
- Kapoor, Seema;
- Gupta, Neerja
Publication type:
Article
Assessment of Post-thaw Quality of Dental Mesenchymal Stromal Cells After Long-Term Cryopreservation by Uncontrolled Freezing.
Published in:
Applied Biochemistry & Biotechnology, 2020, v. 191, n. 2, p. 728, doi. 10.1007/s12010-019-03216-6
By:
- Raik, Shalini;
- Kumar, Ajay;
- Rattan, Vidya;
- Seth, Saurabh;
- Kaur, Anupriya;
- Bhatta charyya, Shalmoli
Publication type:
Article
Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population.
Published in:
Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1155211
By:
- Srivastava, Priyanka;
- Bamba, Chitra;
- Chopra, Seema;
- Rohilla, Minakshi;
- Chaudhry, Chakshu;
- Kaur, Anupriya;
- Panigrahi, Inusha;
- Mandal, Kausik
Publication type:
Article
Cytochrome P450 (CYP2C9*2,*3) & vitamin-K epoxide reductasecomplex (VKORC1 -1639G<A) gene polymorphisms & their effect on acenocoumarol dose in patients with mechanical heart valve replacement.
Published in:
Indian Journal of Medical Research, 2013, v. 137, n. 1, p. 203
By:
- Kaur, Anupriya;
- Khan, Farah;
- Agrawal, Suraksha S.;
- Kapoor, Aditya;
- Agarwal, Surendra K.;
- Phadke, Shubha R.
Publication type:
Article
Parents of Indian Children with Down Syndrome: Stigma and Health Related Quality of Life.
Published in:
2023
By:
- Jogu, Suchit;
- Sharma, Rajni;
- Gupta, Shifali;
- Shah, Ruchita;
- Panigrahi, Inusha;
- Kaur, Anupriya
Publication type:
Letter
X-Linked ALG13 Gene Variant as a Cause of Epileptic Encephalopathy in Girls.
Published in:
2019
By:
- Madaan, Priyanka;
- Negi, Sandeep;
- Sharma, Rajni;
- Kaur, Anupriya;
- Sahu, Jitendra Kumar
Publication type:
Case Study
Analysis of short stature cases referred for genetic evaluation.
Published in:
2012
By:
- Kaur, Anupriya;
- Phadke, Shubha;
- Phadke, Shubha R
Publication type:
journal article
Spectrum of congenital and inherited ocular disorders seen in a genetic clinic: Experience of a developing ocular genetic service.
Published in:
Indian Journal of Ophthalmology, 2023, v. 71, n. 3, p. 935, doi. 10.4103/ijo.IJO_1177_22
By:
- Sahu, Animesh;
- Kaur, Savleen;
- Sukhija, Jaspreet;
- Srivastava, Priyanka;
- Kaur, Anupriya
Publication type:
Article
Ocular presentation of Walker-Warburg syndrome with mutation.
Published in:
2022
By:
- Sukhija, Jaspreet;
- Isher, Harpreet;
- Kaur, Savleen;
- Korla, Shagun;
- Kaur, Anupriya;
- Raj, Srishti;
- Isher, Harpreet Kour
Publication type:
journal article
Fetal Autopsy Showing Two Ventral Body Wall Defects: An Unusual Presentation.
Published in:
Journal of Clinical & Diagnostic Research, 2020, v. 14, n. 10, p. 1, doi. 10.7860/JCDR/2020/18625.14103
By:
- KAUR, ANUPRIYA;
- PRASAD, ARUN;
- PUSHPAJA, JESSY JAYARAMAN;
- KAPOORA, KANCHAN
Publication type:
Article
Medicine Prescribing Preference and Patient Adherence: Perspectives of Indian Medical Practitioners.
Published in:
Journal of Young Pharmacists, 2015, v. 7, p. 446, doi. 10.5530/jyp.2015.4s.6
By:
- Khan, Ahmed Nawaz;
- Kaur, Anupriya;
- Khar, Roop Krishen;
- Khanam, Sadaf
Publication type:
Article
USING CORRESPONDENCE ANALYSIS TO MAP ONLINE PURCHASE CRITERIA OF DIFFERENT PRODUCT CATEGORIES.
Published in:
International Journal of Electronic Commerce Studies, 2020, v. 11, n. 1, p. 45, doi. 10.7903/ijecs.1818
By:
- Thakur, Preeti;
- Kaur, Anupriya
Publication type:
Article
Online Shopping Attitude of Indian Tier 2 Consumers: Some Qualitative Insights.
Published in:
International Journal of Online Marketing, 2019, v. 9, n. 2, p. 1, doi. 10.4018/IJOM.2019040102
By:
- Thakur, Preeti;
- Kaur, Anupriya
Publication type:
Article
How Experts Make a Call: Copy Number Variation Analysis in Unusual/Rare Case Scenarios.
Published in:
Neurology India, 2022, v. 70, n. 1, p. 148, doi. 10.4103/0028-3886.338651
By:
- Srivastava, Priyanka;
- Chaudhry, Chakshu;
- Kaur, Anupriya;
- Phadke, Shubha;
- Panigrahi, Inusha
Publication type:
Article
It is in the face - Have a relook!
Published in:
2020
By:
- Endrakanti, Mounika;
- Kaur, Anupriya;
- Panigrahi, Inusha;
- Pandiarajan, Vignesh
Publication type:
letter
SEM Approach to Teen Influence in Family Decision Making.
Published in:
Contemporary Management Research, 2013, v. 9, n. 3, p. 323, doi. 10.7903/cmr.11080
By:
- Kaur, Anupriya;
- Medury, Yajulu
Publication type:
Article
Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India.
Published in:
Congenital Anomalies, 2021, v. 61, n. 4, p. 140, doi. 10.1111/cga.12414
By:
- Chaudhry, Chakshu;
- Kaur, Parminder;
- Srivastava, Priyanka;
- Panigrahi, Inusha;
- Kaur, Anupriya
Publication type:
Article
Carrier frequency of Spino-muscular atrophy in individuals of a reproductive age group from North India.
Published in:
Journal of Family Medicine & Primary Care, 2022, v. 11, n. 12, p. 7870, doi. 10.4103/jfmpc.jfmpc_869_22
By:
- Kaur, Anupriya;
- Kumari, Anu;
- Kaur, Anit;
- Sharma, Riya;
- Srivastava, Priyanka;
- Suthar, Renu
Publication type:
Article
Association of single nucleotide polymorphism rs113420705 of CASP3 in children with Kawasaki disease from North India.
Published in:
Journal of Family Medicine & Primary Care, 2022, v. 11, n. 9, p. 5404, doi. 10.4103/jfmpc.jfmpc_177_22
By:
- Das, K;
- Bhattarai, Dharmagat;
- Kaur, Anupriya;
- Kaur, Anit;
- Kumrah, Rajni;
- Srivastava, Priyanka;
- Rawat, Amit;
- Singh, Surjit
Publication type:
Article
Editorial: Ehlers-Danlos syndrome: from bedside to bench.
Published in:
Frontiers in Genetics, 2024, p. 01, doi. 10.3389/fgene.2024.1399386
By:
- Tomoki Kosho;
- Shujiro Hayashi;
- Ken-ichi Matsumoto;
- Syx, Delfien;
- Kaur, Anupriya
Publication type:
Article
Chromosome-scale comparative sequence analysis unravels molecular mechanisms of genome dynamics between two wheat cultivars.
Published in:
Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1477-2
By:
- Thind, Anupriya Kaur;
- Wicker, Thomas;
- Müller, Thomas;
- Ackermann, Patrick M.;
- Steuernagel, Burkhard;
- Wulff, Brande B. H.;
- Spannagl, Manuel;
- Twardziok, Sven O.;
- Felder, Marius;
- Lux, Thomas;
- Mayer, Klaus F. X.;
- Keller, Beat;
- Krattinger, Simon G.
Publication type:
Article
Estrogen Receptor 1 Gene Polymorphism and its Association with Idiopathic Short Stature in a North Indian Population.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 3, p. 279, doi. 10.4274/jcrpe.galenos.2024.2023-11-7
By:
- Patel, Ravi Shankar;
- Daniel, Roshan;
- Bhardwaj, Chitra;
- Kumari, Anu;
- Bawa, Pratibha;
- Tyagi, Ankita;
- Dayal, Devi;
- Kaur, Anupriya;
- Panigrahi, Inusha;
- Kaur, Harvinder;
- Srivastava, Priyanka
Publication type:
Article
SHOX Variations in Idiopathic Short Stature in North India and a Review of Cases from Asian Countries.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 1, p. 41, doi. 10.4274/jcrpe.galenos.2023.2023-3-13
By:
- Srivastava, Priyanka;
- Tyagi, Ankita;
- Bhardwaj, Chitra;
- Kumari, Anu;
- Kaur, Harvinder;
- Seth, Saurabh;
- Kaur, Anupriya;
- Panigrahi, Inusha;
- Dayal, Devi;
- Pramanik, Subhodip;
- Mandal, Kausik
Publication type:
Article
X‐linked frontometaphyseal dysplasia with severe scoliosis and spinal cord compromise in an Indian boy.
Published in:
American Journal of Medical Genetics. Part A, 2021, v. 185, n. 5, p. 1550, doi. 10.1002/ajmg.a.62134
By:
- Gangadaran, Prabakaran;
- Chaudhry, Chakshu;
- Panigrahi, Inusha;
- Kumari, Anu;
- Kaur, Anupriya
Publication type:
Article
Ayme gripp syndrome in an Indian patient.
Published in:
American Journal of Medical Genetics. Part A, 2021, v. 185, n. 4, p. 1312, doi. 10.1002/ajmg.a.62053
By:
- Chaudhry, Chakshu;
- Kaur, Parminder;
- Srivastava, Priyanka;
- Kaur, Anupriya
Publication type:
Article
Wolf–Hirschhorn syndrome: A case series from India.
Published in:
American Journal of Medical Genetics. Part A, 2020, v. 182, n. 12, p. 3048, doi. 10.1002/ajmg.a.61856
By:
- Chaudhry, Chakshu;
- Kaur, Anit;
- Panigrahi, Inusha;
- Kaur, Anupriya
Publication type:
Article
Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect.
Published in:
2019
By:
- Vignesh, Pandiarajan;
- Sharma, Madhubala;
- Pilania, Rakesh Kumar;
- Shandilya, Jitendra Kumar;
- Kaur, Anit;
- Goel, Shubham;
- Kaur, Anupriya;
- Suri, Deepti;
- Rawat, Amit;
- Dalal, Ashwin;
- Sarma, Asodu Sandeep;
- Singh, Surjit
Publication type:
Letter
Rapid cloning of genes in hexaploid wheat using cultivar-specific long-range chromosome assembly.
Published in:
Nature Biotechnology, 2017, v. 35, n. 8, p. 793, doi. 10.1038/nbt.3877
By:
- Thind, Anupriya Kaur;
- Wicker, Thomas;
- Šimková, Hana;
- Fossati, Dario;
- Moullet, Odile;
- Brabant, Cécile;
- Vrána, Jan;
- Doležel, Jaroslav;
- Krattinger, Simon G
Publication type:
Article
Gas Chromatography Mass Spectrometry Aided Diagnosis of Glutathione Synthetase Deficiency.
Published in:
Laboratory Medicine, 2022, v. 53, n. 3, p. e59, doi. 10.1093/labmed/lmab084
By:
- Kaur, Parminder;
- Chaudhry, Chakshu;
- Panigrahi, Inusha;
- Srivastava, Priyanka;
- Kaur, Anupriya
Publication type:
Article
Achondroplasia—First Report from India of a Rare FGFR3 Gene Variant.
Published in:
Laboratory Medicine, 2021, v. 52, n. 5, p. 499, doi. 10.1093/labmed/lmaa116
By:
- Chaudhry, Chakshu;
- G, Prabakaran;
- Srivastava, Priyanka;
- Das, Reena;
- Kaur, Jasbir;
- Panigrahi, Inusha;
- Kaur, Anupriya
Publication type:
Article
Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India.
Published in:
Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00613-9
By:
- Sheth, Harsh;
- Nair, Aadhira;
- Bhavsar, Riddhi;
- Kamate, Mahesh;
- Gowda, Vykuntaraju K.;
- Bavdekar, Ashish;
- Kadam, Sandeep;
- Nampoothiri, Sheela;
- Panigrahi, Inusha;
- Kaur, Anupriya;
- Shah, Siddharth;
- Mehta, Sanjeev;
- Jagadeesan, Sujatha;
- Suresh, Indrani;
- Kapoor, Seema;
- Bajaj, Shruti;
- Devi, Radha Rama;
- Prajapati, Ashka;
- Godbole, Koumudi;
- Patel, Harsh
Publication type:
Article
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities.
Published in:
Clinical Genetics, 2021, v. 100, n. 5, p. 542, doi. 10.1111/cge.14037
By:
- Kaur, Parneet;
- do Rosario, Michelle C;
- Hebbar, Malavika;
- Sharma, Suvasini;
- Kausthubham, Neethukrishna;
- Nair, Karthik;
- A, Shrikiran;
- Bhat Y, Ramesh;
- Lewis, Leslie Edward S;
- Nampoothiri, Sheela;
- Patil, Siddaramappa J;
- Suresh, Narayanaswami;
- Bijarnia Mahay, Sunita;
- Dua Puri, Ratna;
- Pai, Shivanand;
- Kaur, Anupriya;
- KC, Rakshith;
- Kamath, Nutan;
- Bajaj, Shruti;
- Kumble, Ali
Publication type:
Article

Found: 39

Financial Literacy of New Job Entrants.

Future Technocrats Perception on Dissemination of Technology.

Indian Youth Inclination towards Unethical Practices in the use of Information and Communication Technology.

Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation.

Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease.

Landscape of genetic infantile epileptic spasms syndrome—A multicenter cohort of 124 children from India.

Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndrome.

Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.

Assessment of Post-thaw Quality of Dental Mesenchymal Stromal Cells After Long-Term Cryopreservation by Uncontrolled Freezing.

Identification of genetic alterations in couples and their products of conceptions from recurrent pregnancy loss in North Indian population.

Cytochrome P450 (CYP2C92,3) & vitamin-K epoxide reductasecomplex (VKORC1 -1639G<A) gene polymorphisms & their effect on acenocoumarol dose in patients with mechanical heart valve replacement.

Parents of Indian Children with Down Syndrome: Stigma and Health Related Quality of Life.

X-Linked ALG13 Gene Variant as a Cause of Epileptic Encephalopathy in Girls.

Analysis of short stature cases referred for genetic evaluation.

Spectrum of congenital and inherited ocular disorders seen in a genetic clinic: Experience of a developing ocular genetic service.

Ocular presentation of Walker-Warburg syndrome with mutation.

Fetal Autopsy Showing Two Ventral Body Wall Defects: An Unusual Presentation.

Medicine Prescribing Preference and Patient Adherence: Perspectives of Indian Medical Practitioners.

USING CORRESPONDENCE ANALYSIS TO MAP ONLINE PURCHASE CRITERIA OF DIFFERENT PRODUCT CATEGORIES.

Online Shopping Attitude of Indian Tier 2 Consumers: Some Qualitative Insights.

How Experts Make a Call: Copy Number Variation Analysis in Unusual/Rare Case Scenarios.

It is in the face - Have a relook!

SEM Approach to Teen Influence in Family Decision Making.

Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India.

Carrier frequency of Spino-muscular atrophy in individuals of a reproductive age group from North India.

Association of single nucleotide polymorphism rs113420705 of CASP3 in children with Kawasaki disease from North India.

Editorial: Ehlers-Danlos syndrome: from bedside to bench.

Chromosome-scale comparative sequence analysis unravels molecular mechanisms of genome dynamics between two wheat cultivars.

Estrogen Receptor 1 Gene Polymorphism and its Association with Idiopathic Short Stature in a North Indian Population.

SHOX Variations in Idiopathic Short Stature in North India and a Review of Cases from Asian Countries.

X‐linked frontometaphyseal dysplasia with severe scoliosis and spinal cord compromise in an Indian boy.

Ayme gripp syndrome in an Indian patient.

Wolf–Hirschhorn syndrome: A case series from India.

Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect.

Rapid cloning of genes in hexaploid wheat using cultivar-specific long-range chromosome assembly.

Gas Chromatography Mass Spectrometry Aided Diagnosis of Glutathione Synthetase Deficiency.

Achondroplasia—First Report from India of a Rare FGFR3 Gene Variant.

Development, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India.

Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities.