M.R.S. Krishnamani - Concepedia

Author

M.R.S. Krishnamani

Vanderbilt University

Also Known As

M R Krishnamani, M R S Krishnamani, M. R. S. Krishnamani, M.R.S. Krishnamani, M.Raja S. Krishnamani

Publications

616

Citations

H-Index

Concepts

All Affiliations

Vanderbilt University Cincinnati Children's Hospital Medical Center

About

M.R.S. Krishnamani is an author at Vanderbilt University specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	296
2	Public Health	3	3	111
3	Engineering	1	1	17
4	Social Sciences	1	1	67
5	Biology	1	1	20

M.R.S. Krishnamani

Publications

578

Citations

H-Index

Page 1

	Year	Citations
DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards Salmo Raskin, John A. Phillips, M.R.S. Krishnamani, American Journal of Medical Genetics	1993	93
Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion Preston W. Campbell, Robert A. Parker, Barbara T. Roberts, The Journal of Pediatrics Tobacco ControlEpidemiologyTobacco UsePoor Clinical StatusSmoking Related Lung Disease	1992	76
Detection of <i>Pseudomonas</i> (<i>Burkholderia</i>) cepacia using PCR Preston W. Campbell, John A. Phillips, Gwendolyn J. Heidecker, Pediatric Pulmonology	1995	71
Heterogeneity in Clinical Manifestation of Autosomal Dominant Neurohypophyseal Diabetes Insipidus Caused by a Mutation Encoding Ala<sup>−1</sup>→Val in the Signal Peptide of the Arginine Vasopressin/Neurophysin II/Copeptin Precursor<sup>1</sup> David R. Repaske, R. Medlej, Ebrû K. Gültekin, The Journal of Clinical Endocrinology & Metabolism GeneticsInsulin SignalingSocial SciencesProgressive Vasopressin DeficiencyHypothalamic Peptide	1997	67
Assignment of the gene (GLCLC) that encodes the heavy subunit of γ-glutamylcysteine synthetase to human chromosome 6 Elaine Sierra‐Rivera, Marshall Summar, Majed Dasouki, Cytogenetic and Genome Research	1995	36
Assignment of the human gene (GLCLR) that encodes the regulatory subunit of γ-glutamylcysteine synthetase to chromosome 1p21 Elaine Sierra‐Rivera, Majed Dasouki, Marshall Summar, Cytogenetic and Genome Research	1996	34
Cystic fibrosis: Relationship between clinical status and F508 deletion Preston W. Campbell, John A. Phillips, M.R.S. Krishnamani, The Journal of Pediatrics FibrosisDisease ProgressionHistopathologyDiagnosisPathology	1991	32
Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35 Marshall Summar, M.J. Dasouki, PR Schofield, Cytogenetic and Genome Research	1995	31
A Novel Arginine Vasopressin-Neurophysin II Mutation Causes Autosomal Dominant Neurohypophyseal Diabetes insipidus and Morphologic Pituitary Changes Nicos Skordis, Philippos C. Patsalis, Joe A. Hettinger, Hormone Research in Paediatrics Genetic DeterminantPituitary GlandFamily MembersGenetic DisorderGenetics	2000	27
Detection of a novel arginine vasopressin defect by dideoxy fingerprinting. M.R.S. Krishnamani, John A. Phillips, Kenneth C. Copeland The Journal of Clinical Endocrinology & Metabolism Functional GenomicsGenetic DisorderMedicineGeneticsPhysiology	1993	27

Page 1