List of works - Sandra Daack-Hirsch

'Information is information': a public perspective on incidental findings in clinical and research genome-based testing

scientific article

A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications

scientific article

A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs

scientific article published on 02 April 2013

A genome wide linkage scan for cleft lip and palate and dental anomalies

article published in 2008

A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23

scientific article

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

scientific article

A practical first step to integrating genetics into the curriculum

scientific article published on 09 March 2012

All things considered, my risk for diabetes is medium: A risk personalization process of familial risk for type 2 diabetes

scientific article published on 23 October 2019

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

scientific article

Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts

scientific article

Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts

scientific article published on 01 January 1999

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate

scientific article

Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families

scientific article published on 10 November 2016

Dermatoglyphic Pattern Types in Subjects with Nonsyndromic Cleft Lip with or without Cleft Palate (CL/P) and Their Unaffected Relatives in the Philippines

scholarly article by Nicole M. Scott et al published July 2005 in Cleft Palate: Craniofacial Journal

Disclosure of incidental genomic findings involving children: are we making progress?

Educating future nursing scientists: Recommendations for integrating omics content in PhD programs.

scientific article

Evaluation of the Perception of Risk Factors for Type 2 Diabetes Instrument in an At-Risk, Nondiabetic Population

scientific article

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

scientific article

Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia

scientific article

Filipino explanatory models of cleft lip with or without cleft palate

scientific article published in March 2010

Five-Year Bibliometric Review of Genomic Nursing Science Research

scientific article published on 2 February 2016

Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia

scientific article

Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting

scientific article

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

scientific article published on 11 June 2009

Impaired FGF signaling contributes to cleft lip and palate

scientific article

Informed consent and genomic incidental findings: IRB chair perspectives

scientific article published on December 2011

Integrating genetics and genomics into nursing curricula: you can do it too!

scientific article

Integrating genomics into undergraduate nursing education

scientific article published on 20 July 2011

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate

scientific article

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

scientific article

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia

scientific article published in 2010

Maternal vitamin B-6 and folate status and risk of oral cleft birth defects in the Philippines

scientific article published in July 2004

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

scientific article

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

scientific article

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

scientific article published on 26 February 2009

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

scientific article

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.

scientific article published in December 2006

Parental perspectives on the diagnostic process for Duchenne and Becker muscular dystrophy

Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

scientific article

Researcher and institutional review board chair perspectives on incidental findings in genomic research

scientific article

Review: `A different type of appointment': the experiences of parents who have children with intellectual disabilities referred for genetic investigation

article

The International Society of Nurses in Genetics (ISONG) 2015 World Congress: Epigenetics Across the Life Span

scientific article published in March 2016

The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice

scientific article published on 10 April 2013

The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations

scientific article published on February 1998

The importance of patient engagement

scientific article published on 13 August 2013

The role of patient engagement in personalized healthcare

Type 2 diabetes familial risk personalization process profiles: Implications for patient-provider communication

scientific article published on 01 August 2019

Women's knowledge and use of prenatal screening tests

scientific article published on 3 August 2016

Working-Class Filipino Women’s Perspectives on Factors That Facilitate or Hinder Prenatal Micronutrients Supplementation to Prevent Congenital Anomalies

article published in 2011

X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.

scientific article

List of works by Sandra Daack-Hirsch

'Information is information': a public perspective on incidental findings in clinical and research genome-based testing

A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications

A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs

A genome wide linkage scan for cleft lip and palate and dental anomalies

A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

A practical first step to integrating genetics into the curriculum

All things considered, my risk for diabetes is medium: A risk personalization process of familial risk for type 2 diabetes

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts

Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate

Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families

Dermatoglyphic Pattern Types in Subjects with Nonsyndromic Cleft Lip with or without Cleft Palate (CL/P) and Their Unaffected Relatives in the Philippines

Disclosure of incidental genomic findings involving children: are we making progress?

Educating future nursing scientists: Recommendations for integrating omics content in PhD programs.

Evaluation of the Perception of Risk Factors for Type 2 Diabetes Instrument in an At-Risk, Nondiabetic Population

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: a subphenotype analysis using two population-based studies of orofacial clefts in Scandinavia

Filipino explanatory models of cleft lip with or without cleft palate

Five-Year Bibliometric Review of Genomic Nursing Science Research

Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia

Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

Impaired FGF signaling contributes to cleft lip and palate

Informed consent and genomic incidental findings: IRB chair perspectives

Integrating genetics and genomics into nursing curricula: you can do it too!

Integrating genomics into undergraduate nursing education

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia

Maternal vitamin B-6 and folate status and risk of oral cleft birth defects in the Philippines

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.

Parental perspectives on the diagnostic process for Duchenne and Becker muscular dystrophy

Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

Researcher and institutional review board chair perspectives on incidental findings in genomic research

Review: `A different type of appointment': the experiences of parents who have children with intellectual disabilities referred for genetic investigation

The International Society of Nurses in Genetics (ISONG) 2015 World Congress: Epigenetics Across the Life Span

The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice

The effect of follow-up on limiting non-participation bias in genetic epidemiologic investigations

The importance of patient engagement

The role of patient engagement in personalized healthcare

Type 2 diabetes familial risk personalization process profiles: Implications for patient-provider communication

Women's knowledge and use of prenatal screening tests

Working-Class Filipino Women’s Perspectives on Factors That Facilitate or Hinder Prenatal Micronutrients Supplementation to Prevent Congenital Anomalies

X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.