Rezultati pretrage autora

1

. . .to a future of genetic medicine od Aravinda Chakravarti

Izdano 2001

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Carta

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2

Nature, nurture and human disease od Aravinda Chakravarti, Peter Little

Izdano 2003

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Artigo

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3

EDNRB/EDN3 and Hirschsprung Disease Type II od Andrew S. McCallion, Aravinda Chakravarti

Izdano 2001

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Revisão

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4

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1. od Francis S. Collins, Lisa Brooks, Aravinda Chakravarti

Izdano 1998

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Artigo

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5

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies od Shin Lin, Aravinda Chakravarti, David J. Cutler

Izdano 2004

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Artigo

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6

Distilling Pathophysiology from Complex Disease Genetics od Aravinda Chakravarti, Andrew G. Clark, Vamsi K. Mootha

Izdano 2013

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Artigo

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7

Undetected Genotyping Errors Cause Apparent Overtransmission of Common Alleles in the Transmission/Disequilibrium Test od Adele A. Mitchell, David J. Cutler, Aravinda Chakravarti

Izdano 2003

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Artigo

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8

Evidence for increased recombination near the human insulin gene: implication for disease association studies. od Aravinda Chakravarti, Steven C. Elbein, M. Alan Permutt

Izdano 1986

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Artigo

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9

Pleiotropic Skeletal and Ocular Phenotypes of the Mouse Mutation Congenital Hydrocephalus (ch/Mf1) Arise from a Winged Helix/Forkhead Transcription Factor Gene od H.-K. Hong, Jonathan H. Lass, Aravinda Chakravarti

Izdano 1999

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Artigo

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10

Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations od Minerva M. Carrasquillo, Joël Zlotogora, Saleh Barges, Aravinda Chakravarti

Izdano 1997

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Artigo

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11

Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC) od Elias Salfati, Alanna C. Morrison, Eric Boerwinkle, Aravinda Chakravarti

Izdano 2015

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Artigo

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12

Linkage Disequilibrium Analysis of Biallelic DNA Markers, Human Quantitative Trait Loci, and Threshold-Defined Case and Control Subjects od Nicholas J. Schork, Swapan K. Nath, Daniele Fallin, Aravinda Chakravarti

Izdano 2000

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Artigo

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13

Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between Ret and Ednrb od Andrew S. McCallion, Erine Stames, Ronald A. Conlon, Aravinda Chakravarti

Izdano 2003

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Artigo

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14

Genomics in Sudden Cardiac Death od Dan E. Arking, Sumeet S. Chugh, Aravinda Chakravarti, Peter M. Spooner

Izdano 2004

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Revisão

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15

Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis od Jeffrey A. Bailey, Laura Carrel, Aravinda Chakravarti, Evan E. Eichler

Izdano 2000

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Artigo

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16

Haplotype Inference in Random Population Samples od Shin Lin, David J. Cutler, Michael E. Zwick, Aravinda Chakravarti

Izdano 2002

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Artigo

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17

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation od Jennifer A. Scott, Sharon L. Wenger, Mark W. Steele, Aravinda Chakravarti

Izdano 1995

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Artigo

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18

Copy Number Variants in Candidate Genes Are Genetic Modifiers of Hirschsprung Disease od Qian Jiang, Yen-Yi Ho, Hao Li, Courtney Berrios, Aravinda Chakravarti

Izdano 2011

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Artigo

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19

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study od Georg Ehret, Ashley O’Connor, Alan B. Weder, Stephen S. Rich, Aravinda Chakravarti

Izdano 2009

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Artigo

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20

Allele Frequency Distributions in Pooled DNA Samples: Applications to Mapping Complex Disease Genes od Sarah H. Shaw, Minerva M. Carrasquillo, Carl Kashuk, Erik G. Puffenberger, Aravinda Chakravarti

Izdano 1998

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Artigo

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. . .to a future of genetic medicine od Aravinda Chakravarti

Nature, nurture and human disease od Aravinda Chakravarti, Peter Little

<i>EDNRB/EDN3</i> and Hirschsprung Disease Type II od Andrew S. McCallion, Aravinda Chakravarti

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1. od Francis S. Collins, Lisa Brooks, Aravinda Chakravarti

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies od Shin Lin, Aravinda Chakravarti, David J. Cutler

Distilling Pathophysiology from Complex Disease Genetics od Aravinda Chakravarti, Andrew G. Clark, Vamsi K. Mootha

Undetected Genotyping Errors Cause Apparent Overtransmission of Common Alleles in the Transmission/Disequilibrium Test od Adele A. Mitchell, David J. Cutler, Aravinda Chakravarti

Evidence for increased recombination near the human insulin gene: implication for disease association studies. od Aravinda Chakravarti, Steven C. Elbein, M. Alan Permutt

Pleiotropic Skeletal and Ocular Phenotypes of the Mouse Mutation Congenital Hydrocephalus (ch/Mf1) Arise from a Winged Helix/Forkhead Transcription Factor Gene od H.-K. Hong, Jonathan H. Lass, Aravinda Chakravarti

Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations od Minerva M. Carrasquillo, Joël Zlotogora, Saleh Barges, Aravinda Chakravarti

Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC) od Elias Salfati, Alanna C. Morrison, Eric Boerwinkle, Aravinda Chakravarti

Linkage Disequilibrium Analysis of Biallelic DNA Markers, Human Quantitative Trait Loci, and Threshold-Defined Case and Control Subjects od Nicholas J. Schork, Swapan K. Nath, Daniele Fallin, Aravinda Chakravarti

Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between <i>Ret</i> and <i>Ednrb</i> od Andrew S. McCallion, Erine Stames, Ronald A. Conlon, Aravinda Chakravarti

Genomics in Sudden Cardiac Death od Dan E. Arking, Sumeet S. Chugh, Aravinda Chakravarti, Peter M. Spooner

Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis od Jeffrey A. Bailey, Laura Carrel, Aravinda Chakravarti, Evan E. Eichler

Haplotype Inference in Random Population Samples od Shin Lin, David J. Cutler, Michael E. Zwick, Aravinda Chakravarti

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation od Jennifer A. Scott, Sharon L. Wenger, Mark W. Steele, Aravinda Chakravarti

Copy Number Variants in Candidate Genes Are Genetic Modifiers of Hirschsprung Disease od Qian Jiang, Yen-Yi Ho, Hao Li, Courtney Berrios, Aravinda Chakravarti

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study od Georg Ehret, Ashley O’Connor, Alan B. Weder, Stephen S. Rich, Aravinda Chakravarti

Allele Frequency Distributions in Pooled DNA Samples: Applications to Mapping Complex Disease Genes od Sarah H. Shaw, Minerva M. Carrasquillo, Carl Kashuk, Erik G. Puffenberger, Aravinda Chakravarti

Rezultati pretrage - Aravinda Chakravarti

. . .to a future of genetic medicine od Aravinda Chakravarti

Nature, nurture and human disease od Aravinda Chakravarti, Peter Little

<i>EDNRB/EDN3</i> and Hirschsprung Disease Type II od Andrew S. McCallion, Aravinda Chakravarti

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1. od Francis S. Collins, Lisa Brooks, Aravinda Chakravarti

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies od Shin Lin, Aravinda Chakravarti, David J. Cutler

Distilling Pathophysiology from Complex Disease Genetics od Aravinda Chakravarti, Andrew G. Clark, Vamsi K. Mootha

Undetected Genotyping Errors Cause Apparent Overtransmission of Common Alleles in the Transmission/Disequilibrium Test od Adele A. Mitchell, David J. Cutler, Aravinda Chakravarti

Evidence for increased recombination near the human insulin gene: implication for disease association studies. od Aravinda Chakravarti, Steven C. Elbein, M. Alan Permutt

Pleiotropic Skeletal and Ocular Phenotypes of the Mouse Mutation Congenital Hydrocephalus (ch/Mf1) Arise from a Winged Helix/Forkhead Transcription Factor Gene od H.-K. Hong, Jonathan H. Lass, Aravinda Chakravarti

Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations od Minerva M. Carrasquillo, Joël Zlotogora, Saleh Barges, Aravinda Chakravarti

Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC) od Elias Salfati, Alanna C. Morrison, Eric Boerwinkle, Aravinda Chakravarti

Linkage Disequilibrium Analysis of Biallelic DNA Markers, Human Quantitative Trait Loci, and Threshold-Defined Case and Control Subjects od Nicholas J. Schork, Swapan K. Nath, Daniele Fallin, Aravinda Chakravarti

Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between <i>Ret</i> and <i>Ednrb</i> od Andrew S. McCallion, Erine Stames, Ronald A. Conlon, Aravinda Chakravarti

Genomics in Sudden Cardiac Death od Dan E. Arking, Sumeet S. Chugh, Aravinda Chakravarti, Peter M. Spooner

Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis od Jeffrey A. Bailey, Laura Carrel, Aravinda Chakravarti, Evan E. Eichler

Haplotype Inference in Random Population Samples od Shin Lin, David J. Cutler, Michael E. Zwick, Aravinda Chakravarti

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation od Jennifer A. Scott, Sharon L. Wenger, Mark W. Steele, Aravinda Chakravarti

Copy Number Variants in Candidate Genes Are Genetic Modifiers of Hirschsprung Disease od Qian Jiang, Yen-Yi Ho, Hao Li, Courtney Berrios, Aravinda Chakravarti

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study od Georg Ehret, Ashley O’Connor, Alan B. Weder, Stephen S. Rich, Aravinda Chakravarti

Allele Frequency Distributions in Pooled DNA Samples: Applications to Mapping Complex Disease Genes od Sarah H. Shaw, Minerva M. Carrasquillo, Carl Kashuk, Erik G. Puffenberger, Aravinda Chakravarti

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