Srikumari, C. R. : rechercher sur Z-Library

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1

Parallel cousin marriages in Madras, Tamil Nadu: New trends in Dravidian kinship

Ramesh, A., Srikumari, C. R., Sukumar, S.

Journal:

Biodemography and Social Biology

Année:

1989

Langue:

english

Fichier:

PDF, 506 KB

english, 1989

2

Gene differentiation at the ABO locus in twenty castes and twenty-two tribes of Andhra Pradesh, India

J. Rajanikumari, C. R. Srikumari

Journal:

American Journal of Physical Anthropology

Année:

1987

Langue:

english

Fichier:

PDF, 328 KB

english, 1987

3

The SNCA (A53T, A30P, E46K) and LRRK2 (G2019S) mutations are rare cause of Parkinson's disease in South Indian patients

M. Vishwanathan Padmaja, Meenakshi Jayaraman, Avathvadi Venkatesan Srinivasan, C.R. Srikumari Srisailapathy, Arabandi Ramesh

Journal:

Parkinsonism & Related Disorders

Année:

2012

Langue:

english

Fichier:

PDF, 103 KB

english, 2012

4

High incidence ofGJB2gene mutations among assortatively mating hearing impaired families in Kerala: future implications

PAVITHRA, AMRITKUMAR, JEFFREY, JUSTIN MARGRET, CHANDRU, JAYASANKARAN, RAMESH, ARABANDI, SRIKUMARI SRISAILAPATHY, C. R.

Journal:

Journal of Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 1.86 MB

english, 2014

5

Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals

Subathra, Mahalingam, Ramesh, Arabandi, Selvakumari, Mathiyalagan, Karthikeyen, N. P., Srisailapathy, C. R. Srikumari

Journal:

Annals of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 1002 KB

english, 2016

6

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

Chen, Achih, Wayne, Sigrid, Bell, Adam, Ramesh, Arabandi, Srisailapathy, C.R. Srikumari, Scott, Daryl A., Sheffield, Val C., Hauwe, Peter Van, Zbar, Ross I. S., Ashley, Jennifer, Lovett, Michael, Camp

Journal:

American Journal of Medical Genetics

Année:

1997

Langue:

english

Fichier:

PDF, 102 KB

english, 1997

7

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31

Greinwald, John H., Wayne, Sigrid, Chen, Achih H., Scott, Daryl A., Zbar, Ross I.S., Kraft, Michelle L., Prasad, Sai, Ramesh, Arabandi, Coucke, Paul, Srisailapathy, C.R. Srikumari, Lovett, Michael, Va

Journal:

American Journal of Medical Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 223 KB

english, 1998

8

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

DA Scott, ML Kraft, R Carmi, A Ramesh, K Elbedour, Y Yairi, C. R. Srikumari Srisailapathy, SS Rosengren, AF Markham, RF Mueller, NJ Lench, G Van Camp, RJH Smith, VC Sheffield

Journal:

Année:

1998

Langue:

english

Fichier:

PDF, 223 KB

english, 1998

9

Acuity of selective mechanisms operating on ABO, Rh, and MN blood groups

C. R. Srikumari, J. Rajanikumari, T. Venkateswara Rao

Journal:

American Journal of Physical Anthropology

Année:

1987

Langue:

english

Fichier:

PDF, 437 KB

english, 1987

10

Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus

Shahid Y. Khan, Zubair M. Ahmed, Muhammad I. Shabbir, Shin-ichiro Kitajiri, Saeeda Kalsoom, Saba Tasneem, Sara Shayiq, Arabandi Ramesh, Srikumari Srisailpathy, Shaheen N. Khan, Richard J.H. Smith, Sai

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 426 KB

english, 2007

11

Genetic admixture studies on fourin situevolved, two migrant and twenty-one ethnic populations of Tamil Nadu, south India

G. SUHASINI, E. SONAA, S. SHILA, C. R. SRIKUMARI, G. JAYARAMAN, A. RAMESH

Journal:

Journal of Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 678 KB

english, 2011

12

Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss

Mani, Ram Shankar, Ganapathy, Aparna, Jalvi, Rajeev, Srikumari Srisailapathy, C R, Malhotra, Vikas, Chadha, Shelly, Agarwal, Arun, Ramesh, Arabandi, Rangasayee, Raghunath Rao, Anand, Anuranjan

Journal:

European Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 294 KB

english, 2008

13

Missense rhodopsin mutation in a family with recessive RP

Kumaramanickavel, Govindasamy, Maw, Marion, Denton, Michael J., John, Sheila, Srikumari, C.R.Srisailapathy, Orth, Ulrike, Oehlmann, Ralph, Gal, Andreas

Journal:

Nature Genetics

Année:

1994

Fichier:

PDF, 247 KB

1994

14

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

Gu, Su-min, Thompson, Debra A., Srikumari, C.R. Srisailapathy, Lorenz, Birgit, Finckh, Ulrich, Nicoletti, Aileen, Murthy, K.R., Rathmann, Michaela, Kumaramanickavel, Govindasamy, Denton, Michael J.

Journal:

Nature Genetics

Année:

1997

Fichier:

PDF, 378 KB

1997

15

Refining the DFNB17 interval in consanguineous Indian families

Yingshi Guo, Valentina Pilipenko, Lynne H.Y. Lim, Hongwei Dou, Liane Johnson, C.R. Srikumari Srisailapathy, Arabandi Ramesh, Daniel I. Choo, Richard J.H. Smith, John H. Greinwald

Journal:

Molecular Biology Reports

Année:

2004

Langue:

english

Fichier:

PDF, 385 KB

english, 2004

16

PARK2 gene mutations in early onset Parkinson's disease patients of South India

M. Vishwanathan Padmaja, Meenakshi Jayaraman, Avathvadi Venkatesan Srinivasan, C.R. Srikumari Srisailapathy, Arabandi Ramesh

Journal:

Neuroscience Letters

Année:

2012

Langue:

english

Fichier:

PDF, 268 KB

english, 2012

17

Passage to India: The search for genes causing autosomal recessive nonsyndromic hearing loss

Ross I.S. Zbar, Arabandi Ramesh, C.R.Srikumari Srisailapathy, Kunihiro Fukushima, Sigrid Wayne, Richard J.H. Smith

Journal:

Otolaryngology - Head and Neck Surgery

Année:

1998

Langue:

english

Fichier:

PDF, 49 KB

english, 1998

18

Refining the DFNB7–DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2

D.A. Scott, S. Drury, R.A. Sundstrom, J. Bishop, R.E. Swiderski, R. Carmi, A. Ramesh, K. Elbedour, C.R. Srikumari Srisailapathy, B.J. Keats, V.C. Sheffield, R.J.H. Smith

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 350 KB

english, 2000

19

Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss-loci on human chromosome 9q and mouse chromosome 19

D.A. Scott, J.H. Greinwald Jr., J.R. Marietta, S. Drury, R.E. Swiderski, A. Viñas, M.M. DeAngelis, R. Carmi, A. Ramesh, M.L. Kraft, K. Elbedour, A.B. Skworak, R.A. Friedman, C.R. Srikumari Srisailapat

Journal:

Année:

1998

Langue:

english

Fichier:

PDF, 220 KB

english, 1998

20

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda M. Peters, Saima Riazuddin, Steve L. Bernstein, Zubair M. Ahmed, Seth L. Ness, Robert Polomeno, Arabandi Ramesh, Melvin Schloss, C. R. Srikumari Srisailpathy, Sigrid Wayne, Susan

Journal:

The American Journal of Human Genetics

Année:

2001

Langue:

english

Fichier:

PDF, 609 KB

english, 2001

21

Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus

Sadaf Naz, Chantal M. Giguere, David C. Kohrman, Kristina L. Mitchem, Saima Riazuddin, Robert J. Morell, Arabandi Ramesh, Srikumari Srisailpathy, Dilip Deshmukh, Sheikh Riazuddin, Andrew J. Griffith,

Journal:

The American Journal of Human Genetics

Année:

2002

Langue:

english

Fichier:

PDF, 292 KB

english, 2002

22

Complete Mitochondrial Genome Analysis and Clinical Documentation of a Five-Generational Indian Family with Mitochondrial 1555A>G Mutation and Postlingual Hearing Loss

Subathra, Mahalingam, Selvakumari, Mathiyalagan, Ramesh, Arabandi, Ramakrishnan, Rajagopalan, Karan, Kalpita Rashmi, Kaur, Manpreet, Manikandan, Mayakannan, Srikumari Srisailapathy, C. R.

Journal:

Annals of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 810 KB

english, 2014

23

Autosomal Dominant Hearing Loss resulting from p.R75Q Mutation in the GJB2 Gene: Nonsyndromic presentation in a South Indian Family

Pavithra, Amritkumar, Selvakumari, Mathiyalagan, Nityaa, Venkatesan, Sharanya, Narasimhan, Ramakrishnan, Rajagopalan, Narasimhan, Murali, Srisailapathy, C.R. Srikumari

Journal:

Annals of Human Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 537 KB

english, 2015

24

Fragile X CGG Repeat Variation in Tamil Nadu, South India: A Comparison of Radioactive and Methylation-Specific Polymerase Chain Reaction in CGG Repeat Sizing

Indhumathi, Nagarathinam, Singh, Deepika, Chong, Samuel S., Thelma, B.K., Arabandi, Ramesh, Srisailpathy, C.R. Srikumari

Journal:

Genetic Testing and Molecular Biomarkers

Année:

2012

Langue:

english

Fichier:

PDF, 581 KB

english, 2012

25

Fertility and mortality differences in relation to maternal body size

Devi, M. Rama, Kumari, J. Rajani, Srikumari, C.R.

Journal:

Annals of Human Biology

Année:

1985

Langue:

english

Fichier:

PDF, 334 KB

english, 1985

26

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness ( dn ) locus

Jain, Pawan K., Fukushima, Kunihiro, Deshmukh, Dilip, Ramesh, Arabandi, Thomas, Elizabeth, Lalwani, Anil K., Kumar, Subrinder, Ploplis, Barbara, Skarka, Hana, Srisailapathy, C.R.Srikumari, Wayne, Sigr

Journal:

Human Molecular Genetics

Année:

1995

Langue:

english

Fichier:

PDF, 1.58 MB

english, 1995

27

Prevalence of aflatoxin B1 in liver biopsies of proven hepatocellular carcinoma in India determined by an in-house immunoperoxidase test

Murugavel, K. G., Naranatt, P. P., Shankar, E. M., Mathews, S., Raghuram, K., Rajasambandam, P., Jayanthi, V., Surendran, R., Murali, A., Srinivas, U., Palaniswamy, K. R., Srikumari, D., Thyagarajan,

Journal:

Journal of Medical Microbiology

Année:

2007

Langue:

english

Fichier:

PDF, 250 KB

english, 2007

28

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

Fukushima, Kunihiro, Ramesh, Arabandi, Srisailapathy, C.R.Srikumari, Ni, Li, Chen, Achih, O'Neill, Marsha, Camp, Guy Van, Coucke, Paul, D.Smith, Shelley, B.Kenyon, Judith, Jain, Pawain, Wilcox, Ed.R.,

Journal:

Human Molecular Genetics

Année:

1995

Langue:

english

Fichier:

PDF, 2.16 MB

english, 1995

29

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

Charizopoulou, Nikoletta, Lelli, Andrea, Schraders, Margit, Ray, Kausik, Hildebrand, Michael S., Ramesh, Arabandi, Srisailapathy, C. R. Srikumari, Oostrik, Jaap, Admiraal, Ronald J. C., Neely, Harold

Journal:

Nature Communications

Année:

2011

Langue:

english

Fichier:

PDF, 1.10 MB

english, 2011

30

AB0 segregation distortion in Visakhapatnam, India

J. Rajani Kumari, C.R. Srikumari and C.Y. Valenzuela

Journal:

Anthropologischer Anzeiger

Année:

1992

Langue:

english

Fichier:

PDF, 967 KB

english, 1992

31

Proportion of low birth weight infants in Visakhapatnam (India) and its relationsship with maternal age, parity and infants survival

J. Rajanikumari, T. Venkateswara Rao and C. R. Srikumari

Journal:

Anthropologischer Anzeiger

Année:

1986

Langue:

english

Fichier:

PDF, 659 KB

english, 1986

32

Rare compound heterozygosity involving dominant and recessive mutations ofGJB2gene in an assortative mating hearing impaired Indian family

Pavithra, Amritkumar, Chandru, Jayasankaran, Jeffrey, Justin Margret, Karthikeyen, N. P., Srisailapathy, C. R. Srikumari

Journal:

European Archives of Oto-Rhino-Laryngology

Année:

2017

Langue:

english

Fichier:

PDF, 1021 KB

english, 2017

33

Familial appraisal of colorblindness in school children of an Indian population

Srikumari, C. R., Rajanikumari, J., Rao, T. Venkateswara

Journal:

Journal of Heredity

Année:

1985

Langue:

english

Fichier:

PDF, 187 KB

english, 1985

34

Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families - an evaluation

Vanniya S, Paridhy, Chandru, Jayasankaran, Pavithra, Amritkumar, Jeffrey, Justin Margret, Kalaimathi, Murugesan, Ramakrishnan, Rajagopalan, Karthikeyen, Natarajan P., C. R. Srikumari, Srisailapathy

Journal:

Annals of Human Genetics

Année:

2017

Langue:

english

Fichier:

PDF, 924 KB

english, 2017

35

The tip link protein Cadherin-23: from hearing loss to cancer

Vanniya. S, Paridhy, Srikumari Srisailapathy, C.R., Kunka Mohanram, Ramkumar

Journal:

Pharmacological Research

Année:

2018

Langue:

english

Fichier:

PDF, 857 KB

english, 2018

36

A Study on Telugu – Speaking Immigrants of Tamil Nadu, South India

Vijaya, M., Kanthimathi, S., Srikumari, C.R., Reddy, P. Govinda, Majumder, P.P., Ramesh, A.

Journal:

International Journal of Human Genetics

Année:

2007

Langue:

english

Fichier:

PDF, 153 KB

english, 2007

37

Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE

Ganapathy, Aparna, Pandey, Nishtha, Srisailapathy, C. R. Srikumari, Jalvi, Rajeev, Malhotra, Vikas, Venkatappa, Mohan, Chatterjee, Arunima, Sharma, Meenakshi, Santhanam, Rekha, Chadha, Shelly, Ramesh,

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 2.83 MB

english, 2014

38

A Genetic Structure of the Early Immigrants (Mukkalathor) of Tamil Nadu as Inferred From Autosomal Loci

Kanthimathi, S., Vijaya, M., Srikumari, C.R., Reddy, P. Govinda, Majumder, P.P., Ramesh, A.

Journal:

International Journal of Human Genetics

Année:

2007

Langue:

english

Fichier:

PDF, 172 KB

english, 2007

39

Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India

Amritkumar, Pavithra, Jeffrey, Justin Margret, Chandru, Jayasankaran, Vanniya S, Paridhy, Kalaimathi, M., Ramakrishnan, Rajagopalan, Karthikeyen, N. P., Srikumari Srisailapathy, C. R.

Journal:

BMC Medical Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 5.88 MB

english, 2018

40

Genetic epidemiology of stuttering among school children in the state of Tamil Nadu, India

Nandhini Devi, G., Thalamuthu, Anbupalam, Valarmathi, S., Karthikeyen, N.P., Srikumari Srisailapathy, C.R.

Journal:

Journal of Fluency Disorders

Année:

2018

Langue:

english

Fichier:

PDF, 1.01 MB

english, 2018

41

Association of ABO and Rh(D) Blood Groups with Filariasis

Srisailapathy, Srikumari, Ramesh, A., Ganesan, J.

Journal:

Année:

1990

Fichier:

PDF, 559 KB

1990

42

Association of ABO and Rh(D) Blood Groups with Filariasis

Srisailapathy, Srikumari, Ramesh, A., Ganesan, J.

Journal:

Année:

1990

Langue:

english

Fichier:

PDF, 559 KB

english, 1990

43

Genetic analysis of SLC26A4 gene (pendrin) related deafness among a cohort of assortative mating families from southern India

Chandru, Jayasankaran, Jeffrey, Justin Margret, Pavithra, Amritkumar, Vanniya, S. Paridhy, Devi, G. Nandhini, Mahalingam, Subathra, Karthikeyen, Natarajan Padmavathy, Srisailapathy, C. R. Srikumari

Journal:

European Archives of Oto-Rhino-Laryngology

Année:

2020

Fichier:

PDF, 2.33 MB

2020

44

Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India

KALAIMATHI, MURUGESAN, SUBATHRA, MAHALINGAM, JEFFREY, JUSTIN MARGRET, SELVAKUMARI, MATHIYALAGAN, CHANDRU, JAYASANKARAN, SHARANYA, NARASIMHAN, PARIDHY, VANNIYA S., SRISAILAPATHY, C. R. SRIKUMARI

Journal:

Journal of Genetics

Année:

2020

Fichier:

PDF, 952 KB

2020