I. Ahmad

发表

Progress and Prospects in Capsicum Breeding for Biotic and Abiotic Stresses

N. Ramchiary, V. Jaiswal, S. Chhapekar, 2018 .

Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci

A. Uitterlinden, J. Erdmann, W. Lieb, 2018, European Journal of Human Genetics.

ICP-MS based analysis of mineral elements composition during fruit development in Capsicum germplasm

N. Ramchiary, A. Rawoof, I. Ahmad, 2021, Journal of Food Composition and Analysis.

Analysis of bioactive components in Ghost chili (Capsicum chinense) for antioxidant, genotoxic, and apoptotic effects in mice

N. Ramchiary, S. Chhapekar, Sarpras M, 2018, Drug and chemical toxicology.

Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

N. Tommerup, H. Eiberg, S. Rehman, 2011, neurogenetics.

Integrated analysis of DNA methylation, transcriptome, and global metabolites in interspecific heterotic Capsicum F1 hybrid

N. Ramchiary, V. Jaiswal, Vijay Gahlaut, 2022, iScience.

Integrated omics analysis identified genes and their splice variants involved in fruit development and metabolites production in Capsicum species

N. Ramchiary, V. Jaiswal, A. Rawoof, 2022, Functional & Integrative Genomics.

NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes

S. Baig, J. Rendu, J. Fauré, 2022, Molecular Genetics and Genomics.

A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia

S. Baig, M. Rasool, Muhammad Tariq, 2008, Journal of Human Genetics.

Linking Omics Approaches to Medicinal Plants and Human Health

M. K. Swamy, N. Ramchiary, Ajay Kumar, 2019, Natural Bio-active Compounds.

Comparative analysis of developmental changes of fruit metabolites, antioxidant activities and mineral elements content in Bhut jolokia and other Capsicum species

N. Ramchiary, A. Rawoof, I. Ahmad, 2019, LWT.

Diversity and expression analysis of ZIP transporters and associated metabolites under zinc and iron stress in Capsicum.

N. Ramchiary, Priyanka, A. Rawoof, 2023, Plant physiology and biochemistry : PPB.

Capsicum chinense MYB Transcription Factor Genes: Identification, Expression Analysis, and Their Conservation and Diversification With Other Solanaceae Genomes

N. Ramchiary, A. Rawoof, I. Ahmad, 2021, Frontiers in Plant Science.

Identification and expression analysis of phosphate transporter genes and metabolites in response to phosphate stress in Capsicum annuum

N. Ramchiary, A. Rawoof, I. Ahmad, 2021 .

Screening of Elite Chickpea Germplasm against Ascochyta Blight under Controlled Conditions

M. T. Mahmood, I. Ahmad, Azhar Iqbal, 2021, Pakistan Journal of Agricultural Research.

Identification of genes involved in fruit development/ripening in Capsicum and development of functional markers.

Nitin Kumar, N. Ramchiary, V. Jaiswal, 2019, Genomics.

Report of Hermansky–Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes

M. Owais, F. Bibi, M. Jelani, 2023, Genes.

CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly.

A. Noegel, P. Frommolt, S. Baig, 2013, Human molecular genetics.

Epigenome Landscape in Capsicum Genome

N. Ramchiary, A. Rawoof, I. Ahmad, 2019, Compendium of Plant Genomes.

Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

H. Bolz, A. Koschak, S. Baig, 2011, Nature Neuroscience.

Noncoding RNAs in Capsicum Genome

N. Ramchiary, A. Rawoof, Mukesh Nitin, 2019, Compendium of Plant Genomes.

Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases

F. Bibi, Jingyun Yang, Chuntao Zhao, 2023, Genes.

OSTEOSYNTHESIS OF SUBTROCHANTERIC FRACTURES USING PROXIMAL FEMORAL NAIL : A PROSPECTIVE STUDY

I. Ahmad, N. Shah, Shah, 2019 .

Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy

Peter Nürnberg, Ingrid Hoffmann, Matthew E Hurles, 2014, Nature Genetics.

Salt induced changes in leaf phenology of wheat plants are regulated by accumulation and distribution pattern of Na+ ion.

J. Akhtar, Z. A. Saqib, I. Ahmad, 2012 .

CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly

A. Noegel, S. Baig, P. Nürnberg, 2016, Molecular Genetics and Genomics.

A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function.

H. Hennies, A. Noegel, P. Frommolt, 2012, American journal of human genetics.

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family

S. Z. Jamal, J. Erdmann, S. Baig, 2021, Genes.

Proteomics of Reproductive Development, Fruit Ripening, and Stress Responses in Tomato.

N. Ramchiary, A. Rawoof, Arunandan Kumar, 2022, Journal of agricultural and food chemistry.

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

A. Noegel, S. Baig, P. Nürnberg, 2020, Molecular genetics & genomic medicine.

Genetic heterogeneity in Pakistani microcephaly families revisited

G. Nürnberg, P. Nürnberg, J. Altmüller, 2017, Clinical genetics.

Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci

A. Uitterlinden, J. Erdmann, W. Lieb, 2018, European Journal of Human Genetics.

Rationality of using various physiological and yield related traits in determining salt tolerance in wheat

J. Akhtar, Z. A. Saqib, I. Ahmad, 2012 .

The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans

J. Erdmann, S. Baig, R. Hartig, 2023, Scientific reports.

A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family

J. Erdmann, G. Nürnberg, J. Altmüller, 2022, Journal of Human Genetics.

Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy

S. Z. Jamal, J. Erdmann, P. Nürnberg, 2023, Clinical genetics.