Katta, Mohan A.V.S.: search on Z-Library

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1

CicArVarDB: SNP and InDel database for advancing genetics research and breeding applications in chickpea

Doddamani, Dadakhalandar, Khan, Aamir W., Katta, Mohan A. V. S. K, Agarwal, Gaurav, Thudi, Mahendar, Ruperao, Pradeep, Edwards, David, Varshney, Rajeev K.

Journal:

Year:

2015

Language:

english

File:

PDF, 910 KB

english, 2015

2

Genomic Testing for Diagnosis of Genetic Disorders in Children: Chromosomal Microarray and NextâGeneration Sequencing

Narayanan, Dhanya Lakshmi, Girisha, Katta Mohan

Journal:

Indian Pediatrics

Year:

2020

File:

PDF, 516 KB

2020

3

Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta

Mrosk, Julia, Gandham, SriLakshmi Bhavani, Shah, Hitesh, Hecht, Jochen, Krüger, Ulrike, Shukla, Anju, Kornak, Uwe, Girisha, Katta Mohan

Journal:

Year:

2018

Language:

english

File:

PDF, 2.48 MB

english, 2018

4

Whole Genome Sequencing and Comparative Genomic Analysis Reveal Allelic Variations Unique to a Purple Colored Rice Landrace (Oryza sativa ssp. indica cv. Purpleputtu)

Lachagari, V. B. Reddy, Gupta, Ravi, Lekkala, Sivarama Prasad, Mahadevan, Lakshmi, Kuriakose, Boney, Chakravartty, Navajeet, Mohan Katta, A. V. S. K., Santhosh, Sam, Reddy, Arjula R., Thomas, George

Journal:

Frontiers in Plant Science

Year:

2019

Language:

english

File:

PDF, 5.22 MB

english, 2019

5

Untapped opportunities for rare disease gene discovery in India

Girisha, Katta Mohan, Pande, Shruti, Dalal, Ashwin, Phadke, Shubha R.

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 643 KB

2020

6

Secondary metabolites from spice and herbs as potential multitarget inhibitors of SARS-CoV-2 proteins

Gupta, Saurabh, Singh, Vishal, Varadwaj, Pritish Kumar, Chakravartty, Navajeet, Katta, A. V. S. Krishna Mohan, Lekkala, Sivarama Prasad, Thomas, George, Narasimhan, Srinivasan, Reddy, Arjula R., Reddy

Journal:

Journal of Biomolecular Structure and Dynamics

Year:

2020

File:

PDF, 3.94 MB

2020

7

Genetic Disorders with Central Nervous System White Matter Abnormalities: An Update

Shukla, Anju, Kaur, Parneet, Narayanan, Dhanya Lakshmi, Rosario, Michelle C., Kadavigere, Rajagopal, Girisha, Katta Mohan

Journal:

Clinical Genetics

Year:

2020

File:

PDF, 1.53 MB

2020

8

A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B gene

Girisha, Katta Mohan, Kortüm, Fanny, Shah, Hitesh, Alawi, Malik, Dalal, Ashwin, Bhavani, Gandham SriLakshmi, Kutsche, Kerstin

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.77 MB

english, 2015

9

Effect of previous heat treatment on ionic conductivity of yttrium-doped KBr crystals

B. Jagan Mohan Reddy, Katta Narasimha Reddy

Journal:

Materials Science and Engineering: B

Year:

1993

Language:

english

File:

PDF, 318 KB

english, 1993

10

Mucolipidosis type II α/β with a homozygous missense mutation in the GNPTAB gene

Maria Francisca Coutinho, Liliana da Silva Santos, Katta Mohan Girisha, Kapaettu Satyamoorthy, Lúcia Lacerda, Maria João Prata, Sandra Alves

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 206 KB

english, 2012

11

Spastic Paraplegia Type 56 in a Young Child

Samaddar, Sukla, Kaur, Parneet, Rajagopal, K. V., Girisha, Katta Mohan, Shukla, Anju, Sharma, Suvasini

Journal:

Indian Journal of Pediatrics

Year:

2020

File:

PDF, 147 KB

2020

12

Effect of modifier oxides on spectroscopic and optical properties of Pr3+ doped PbO-Ro2O3âWO3âB2O3 glasses (with Ro2O = Sb2O3, Al2O3, and Bi2O3)

Prasad, R.N.A., Venkata Siva, Bathula, Neeraja, Katta, Krishna Mohan, Nutakki, Rojas, Jose I.

Journal:

Journal of Luminescence

Year:

2021

File:

PDF, 5.04 MB

2021

13

Mutation spectrum of COL1A1 and COL1A2 genes in Indian patients with osteogenesis imperfecta

Stephen, Joshi, Shukla, Anju, Dalal, Ashwin, Girisha, Katta Mohan, Shah, Hitesh, Gupta, Neerja, Kabra, Madhulika, Dabadghao, Preeti, Phadke, Shubha R.

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 539 KB

english, 2014

14

White matter changes in GM1 gangliosidosis

Tuteja, Moni, Bidchol, Abdul Mueed, Girisha, Katta Mohan, Phadke, Shubha R.

Journal:

Indian Pediatrics

Year:

2015

Language:

english

File:

PDF, 420 KB

english, 2015

15

Familial 7q11.23 duplication with variable phenotype

Patil, Siddaramappa J., Salian, Smrithi, Bhat, Venkaraman, Girisha, Katta Mohan, Shrivastava, Yash, VS, Kiran, Sapare, Anilkumar

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 367 KB

english, 2015

16

Further characterization of acro-renal-uterine-mandibular syndrome

Girisha, Katta Mohan, Pratap, Deepika, Shah, Hitesh H.

Journal:

Clinical Dysmorphology

Year:

2012

Language:

english

File:

PDF, 143 KB

english, 2012

17

[BMJ Publishing Group Ltd and European League Against Rheumatism Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12â15 June 2019 - ()] Paediatric rheumatology - FRI0578âLACC1 MUTATION IN THREE SIBLINGS WITH POLYARTHRITIS WITHOUT SYSTEMIC MANIFESTATIONS

Singh, Ankita, Suri, Deepti, Jacob, Prince, Girisha, Katta Mohan, Jindal, Ankur, Singh, Surjit

Year:

2019

File:

PDF, 56 KB

2019

18

A Novel Bi‐allelic Loss‐of‐Function Variant in MYOD1 : Further evidence for gene‐disease association and phenotypic variability in MYOD1 related myopathy

Shukla, Anju, Narayanan, Dhanya Lakshmi, Asher, Urja, Girisha, Katta Mohan

Journal:

Clinical Genetics

Year:

2019

Language:

english

File:

PDF, 1.04 MB

english, 2019

19

Next generation sequencing andde novotranscriptome analysis ofCostus pictusD. Don, a non-model plant with potent anti-diabetic properties

Annadurai, Ramasamy S, Jayakumar, Vasanthan, Mugasimangalam, Raja C, Katta, Mohan AVSK, Anand, Sanchita, Gopinathan, Sreeja, Sarma, Santosh, Fernandes, Sunjay, Mullapudi, Nandita, Murugesan, S, Rao, S

Journal:

Year:

2012

Language:

english

File:

PDF, 1.07 MB

english, 2012

20

Synthesis of Some Fused Pyrazoles and Isoxazoles

Padmavathi, Venkatapuram, Reddy, Boggu Jagan Mohan, Balaiah, Akula, Reddy, Katta Venugopal, Reddy, Dandu Bhaskar

Journal:

Year:

2000

Language:

english

File:

PDF, 46 KB

english, 2000

21

Expanding the phenotype associated with 17q12 duplication: Case report and review of the literature

Bierhals, Tatjana, Maddukuri, Satish Babu, Kutsche, Kerstin, Girisha, Katta Mohan

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 230 KB

english, 2013

22

BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia

Cho, Sung Yoon, Bae, Jun-Seok, Kim, Nayoung K.D., Forzano, Francesca, Girisha, Katta Mohan, Baldo, Chiara, Faravelli, Francesca, Cho, Tae-Joon, Kim, Dongsup, Lee, Kyoung Yeul, Ikegawa, Shiro, Shim, Jo

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 786 KB

english, 2016

23

The promise of discovering population-specific disease-associated genes in South Asia

Nakatsuka, Nathan, Moorjani, Priya, Rai, Niraj, Sarkar, Biswanath, Tandon, Arti, Patterson, Nick, Bhavani, Gandham SriLakshmi, Girisha, Katta Mohan, Mustak, Mohammed S, Srinivasan, Sudha, Kaushik, Ami

Journal:

Nature Genetics

Year:

2017

Language:

english

File:

PDF, 1.05 MB

english, 2017

24

Confirmation of a rare genetic leukoencephalopathy due to a novel Bi-allelic variant in RPIA

Kaur, Parneet, Wamelink, Mirjam M.C., van der Knaap, Marjo S., Girisha, Katta Mohan, Shukla, Anju

Journal:

European Journal of Medical Genetics

Year:

2019

Language:

english

File:

PDF, 1.52 MB

english, 2019

25

Mutations in patients with osteogenesis imperfecta from consanguineous Indian families

Stephen, Joshi, Girisha, Katta Mohan, Dalal, Ashwin, Shukla, Anju, Shah, Hitesh, Srivastava, Priyanka, Kornak, Uwe, Phadke, Shubha R.

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 1.53 MB

english, 2015

26

Association of Gene with Cytoplasmic Male Sterility in Pigeonpea

Sinha, Pallavi, Saxena, K. B., Saxena, Rachit K., Singh, Vikas K., Suryanarayana, V., Sameer Kumar, C.V., Katta, Mohan A.V.S., Khan, Aamir W., Varshney, Rajeev K.

Journal:

The Plant Genome

Year:

2015

Language:

english

File:

PDF, 1.60 MB

english, 2015

27

Ionic Conductivity Studies in Yttrium-doped KCl Crystals

B. Jagan Mohan Reddy, MD. Shareefuddin, M. Narasimha Chary, Katta Narasimha Reddy

Journal:

Crystal Research and Technology

Year:

1993

Language:

english

File:

PDF, 221 KB

english, 1993

28

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

Katta Mohan Girisha, Saadi Abdul Vahab, Ashwin B. Dalal, P. M. Gopinath, K. Satyamoorthy

Journal:

Annals of Hematology

Year:

2010

Language:

english

File:

PDF, 94 KB

english, 2010

29

Eight years experience from a skeletal dysplasia referral center in a tertiary hospital in Southern India: A model for the diagnosis and treatment of rare diseases in a developing country

Nampoothiri, Sheela, Yesodharan, Dhanya, Sainulabdin, Gazel, Narayanan, Dhanyalakshmi, Padmanabhan, Laxmi, Girisha, Katta Mohan, Cathey, Sara S., De Paepe, Anne, Malfait, Fransiska, Syx, Delfien, Henn

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 114 KB

english, 2014

30

Milder form of pachydermoperiostosis: a report of four cases

Girisha, Katta Mohan, Mandal, Kausik, Phadke, Shubha Rajendra

Journal:

Clinical Dysmorphology

Year:

2009

Language:

english

File:

PDF, 315 KB

english, 2009

31

Influence of metal oxides on spectroscopic features of Nd2O3 doped PbOâMo2O3âWO3âB2O3 glasses

Prasad, R.N.A., Siva, Bathula Venkata, Neeraja, Katta, Mohan, N. Krishna, Rojas, Jose I.

Journal:

Journal of Luminescence

Year:

2020

File:

PDF, 1.24 MB

2020

32

Identification of Prophages in Bacterial Genomes by Dinucleotide Relative Abundance Difference

Srividhya, K. V., Alaguraj, V., Poornima, G., Kumar, Dinesh, Singh, G. P., Raghavenderan, L., Katta, A. V. S. K. Mohan, Mehta, Preeti, Krishnaswamy, S., Sussman, Joel

Journal:

Year:

2007

Language:

english

File:

PDF, 295 KB

english, 2007

33

Recurrent bi-allelic splicing variant c.454+3A>G in TRAPPC4 is associated with progressive encephalopathy and muscle involvement

Kaur, Parneet, Kadavigere, Rajagopal, Girisha, Katta Mohan, Shukla, Anju

Journal:

Year:

2020

File:

PDF, 321 KB

2020

34

A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathy

Girisha, Katta Mohan, Shukla, Anju, Trujillano, Daniel, Bhavani, Gandham SriLakshmi, Hebbar, Malavika, Kadavigere, Rajagopal, Rolfs, Arndt

Journal:

Clinical Genetics

Year:

2016

Language:

english

File:

PDF, 448 KB

english, 2016

35

Deciphering the transcriptomic insight during organogenesis in Castor (Ricinus communis L.), Jatropha (Jatropha curcas L.) and Sunflower (Helianthus annuus L.)

Puvvala, Sai Sudha, Muddanuru, Tarakeswari, Thangella, Padmavathi A. V., Kumar, O. Aniel, Chakravartty, Navajeet, Vettath, Vineeth Kodengil, Katta, A. V. S. K. Mohan, Lekkala, Sivarama Prasad, Kuriako

Journal:

Year:

2019

Language:

english

File:

PDF, 3.53 MB

english, 2019

36

Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails

Girisha, Katta Mohan, Vasudevan, Thanvanthri Gururajan, Saadi, Abdul Vahab, Shah, Hitesh, Gopinath, Puthiya Mundyat, Satyamoorthy, Kapaettu

Journal:

Clinical Dysmorphology

Year:

2011

Language:

english

File:

PDF, 168 KB

english, 2011

37

Reversible sperm changes in an abstinent alcoholic

Katta, Balaraju B, Taneja, Neelum, Mohan, D

Journal:

Irish Journal of Psychological Medicine

Year:

1990

Language:

english

File:

PDF, 147 KB

english, 1990

38

Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients

Girisha, Katta Mohan, Bidchol, Abdul Mueed, Graul-Neumann, Luitgard, Gupta, Ashish, Hehr, Ute, Lessel, Davor, Nader, Sean, Shah, Hitesh, Wickert, Julia, Kutsche, Kerstin

Journal:

BMC Medical Genetics

Year:

2016

Language:

english

File:

PDF, 1.79 MB

english, 2016

39

Novel variant p.(Ala102Thr) in SDHB causes mitochondrial complex II deficiency: Case report and review of the literature

Kaur, Parneet, Sharma, Suvasini, Kadavigere, Rajagopal, Girisha, Katta Mohan, Shukla, Anju

Journal:

Annals of Human Genetics

Year:

2020

File:

PDF, 819 KB

2020

40

Prioritization of candidate genes in “QTL-hotspot” region for drought tolerance in chickpea (Cicer arietinum L.)

Kale, Sandip M, Jaganathan, Deepa, Ruperao, Pradeep, Chen, Charles, Punna, Ramu, Kudapa, Himabindu, Thudi, Mahendar, Roorkiwal, Manish, Katta, Mohan AVSK, Doddamani, Dadakhalandar, Garg, Vanika, Kisho

Journal:

Scientific Reports

Year:

2015

Language:

english

File:

PDF, 1.78 MB

english, 2015

41

CicArMiSatDB: the chickpea microsatellite database

Dadakhalandar Doddamani,Mohan AVSK Katta,Aamir W Khan…

Journal:

BMC Bioinformatics

Year:

2014

Language:

english

File:

PDF, 1.23 MB

english, 2014

42

De Novo Transcriptome Assembly (NGS) of Curcuma longa L. Rhizome Reveals Novel Transcripts Related to Anticancer and Antimalarial Terpenoids

Annadurai, Ramasamy S., Neethiraj, Ramprasad, Jayakumar, Vasanthan, Damodaran, Anand C., Rao, Sudha Narayana, Katta, Mohan A. V. S. K., Gopinathan, Sreeja, Sarma, Santosh Prasad, Senthilkumar, Vanitha

Journal:

Year:

2013

Language:

english

File:

PDF, 624 KB

english, 2013

43

Report of second case and clinical and molecular characterization of Eiken syndrome

Moirangthem, Amita, Narayanan, Dhanya Lakshmi, Jacob, Prince, Nishimura, Gen, Mortier, Geert, Girisha, Katta Mohan

Journal:

Clinical Genetics

Year:

2018

Language:

english

File:

PDF, 698 KB

english, 2018

44

Probabilistic Seismic Hazard Assessment of Mangalore and Its Adjoining Regions, A Part of Indian Peninsular: An Intraplate Region

Shreyasvi, C., Venkataramana, Katta, Chopra, Sumer, Rout, Madan Mohan

Journal:

Pure and Applied Geophysics

Year:

2019

Language:

english

File:

PDF, 3.51 MB

english, 2019

45

Homozygous variant, p.(Arg643Trp) in VAC14 causes striatonigral degeneration: report of a novel variant and review of VAC14-related disorders

Kaur, Parneet, Bhavani, Gandham SriLakshmi, Raj, Arun, Girisha, Katta Mohan, Shukla, Anju

Journal:

Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 1.25 MB

english, 2019

46

Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature

Upadhyai, Priyanka, Amiri, Eram Fatima, Guleria, Vishal Singh, Bielas, Stephanie L., Girisha, Katta Mohan, Shukla, Anju

Journal:

Clinical Dysmorphology

Year:

2020

File:

PDF, 400 KB

2020

47

[IEEE 2016 IEEE 6th International Conference on Power Systems (ICPS) - New Delhi, India (2016.3.4-2016.3.6)] 2016 IEEE 6th International Conference on Power Systems (ICPS) - Fault-tolerant energy scheduling system

Mahendra, Lagineni, Mohan, Katta Jagan, Kumar, R.K. Senthil, Prasad, G.L. Ganga

Year:

2016

Language:

english

File:

PDF, 478 KB

english, 2016

48

Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia, and skeletal abnormalities: A novel phenotype

Hitesh Shah, Susanne Bens, Almuth Caliebe, John M. Graham Jr, Katta Mohan Girisha

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 641 KB

english, 2012

49

Metatropic dysplasia with a novel mutation inTRPV4

Narayanan, Dhanya Lakshmi, Bhavani, Gandham SriLakshmi, Girisha, Katta Mohan, Phadke, Shubha R.

Journal:

Indian Pediatrics

Year:

2016

Language:

english

File:

PDF, 513 KB

english, 2016

50

[IEEE 2017 IEEE PES Asia-Pacific Power and Energy Engineering Conference (APPEEC) - Bangalore, India (2017.11.8-2017.11.10)] 2017 IEEE PES Asia-Pacific Power and Energy Engineering Conference (APPEEC) - Deviation settlement mechanism based real-time energy assessment system for open access user

Mahendra, Lagineni, Mohan, Katta Jagan, Kumar, R. K. Senthil, Bindhumadhava, B. S.

Year:

2017

Language:

english

File:

PDF, 971 KB

english, 2017

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