S. Daack-Hirsch

发表

M. Seven, L. Shah, H. Yazici, 2020, Cancer nursing.

‘Information is information’: a public perspective on incidental findings in clinical and research genome‐based testing

M. Driessnack, S. Daack-Hirsch, A. Hanish, 2013, Clinical genetics.

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Jeffrey C. Murray, Michael J. Dixon, Andrew C. Lidral, 2002, Nature Genetics.

Dermatoglyphic Fingerprint Heterogeneity Among Individuals with Nonsyndromic Cleft Lip With or Without Cleft Palate and Their Unaffected Relatives in China and the Philippines

Nicole M. Scott, S. Weinberg, K. Neiswanger, 2005, Human biology.

Clinical and epidemiologic studies of cleft lip and palate in the Philippines.

K. Buetow, R. Munger, J. Murray, 1997, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

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

A. Jugessur, S. Weinberg, K. Neiswanger, 2009, American journal of human genetics.

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

S. Daack-Hirsch, Henrietta Gamboa, 2012, Asia-Pacific journal of public health.

The role of patient engagement in personalized healthcare.

S. Daack-Hirsch, Colleen Campbell, 2014, Personalized medicine.

Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate

M. Marazita, J. Murray, W. Fakhouri, 2012, PloS one.

Discordant MZ Twins With Cleft Lip and Palate: A Model for Identifying Genes in Complex Traits

N. Martin, D. Boomsma, K. Christensen, 2005, Twin Research and Human Genetics.

Mental Models of Cause and Inheritance for Type 2 Diabetes Among Unaffected Individuals Who Have a Positive Family History

L. Shah, S. Daack-Hirsch, Lisa L. Shah, 2018, Qualitative health research.

Targeted scan of fifteen regions for nonsyndromic cleft lip and palate in Filipino families

M. Marazita, S. Daack-Hirsch, E. O’Brien, 2004, American journal of medical genetics. Part A.

Family Relationships Associated With Communication and Testing for Inherited Cardiac Conditions

Anne L. Ersig, Ferhaan Ahmad, Janet K. Williams, 2018, Western journal of nursing research.

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

M. Marazita, J. Murray, S. Daack-Hirsch, 2008, Genetics in Medicine.

Five-Year Bibliometric Review of Genomic Nursing Science Research.

Janet K. Williams, S. Daack-Hirsch, T. Tripp-Reimer, 2016, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

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

K. Christensen, M. Marazita, J. Murray, 2007, American journal of medical genetics. Part A.

Development and psychometric testing of the dyadic communication observational coding scheme in DEmentia care (DCODE): family dyadic communication in dementia.

K. Williams, S. Daack-Hirsch, Wen Liu, 2022, Aging & mental health.

Parent-Child Communication about Congenital Adrenal Hyperplasia: Filipino Mothers’ Experience

S. Daack-Hirsch, C. Padilla, M. Laurino, 2017 .

Experiences of BRCA1/2 Gene Mutation-Positive Women With Cancer in Communicating Genetic Risk to Their Relatives.

M. Seven, L. Shah, H. Yazici, 2020, Cancer nursing.

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.

S. Patil, B. Bjork, J. Murray, 1999, American journal of medical genetics.

Genome-wide analysis of copy number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes.

Lisa A. Lansdon, K. Mohlke, S. Girirajan, 2022, American journal of human genetics.

Maternal alcohol use and risk of orofacial cleft birth defects.

R. Munger, J. Murray, T. Burns, 1996, Teratology.

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

K. Christensen, J. Murray, S. Daack-Hirsch, 2003, Journal of medical genetics.

Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome.

E. Roeder, J. Murray, A. Lin, 2000, American journal of medical genetics.

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

R. Ferrell, J. Murray, W. Alward, 1998, Nature Genetics.

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

J. Murray, H. van Bokhoven, R. Gorlin, 2002, Journal of medical genetics.

Impaired FGF signaling contributes to cleft lip and palate

B. Maher, M. Marazita, M. Mohammadi, 2007, Proceedings of the National Academy of Sciences.

Maternal Genes and Facial Clefts in Offspring: A Comprehensive Search for Genetic Associations in Two Population-Based Cleft Studies from Scandinavia

Min Shi, Kaare Christensen, Astanand Jugessur, 2010, PloS one.

Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate

M. Marazita, J. Murray, D. Fitzpatrick, 2005, PLoS genetics.

Discordant MZ twins with cleft lip and palate: a model for identifying genes in complex traits.

N. Martin, D. Boomsma, K. Christensen, 2004, Twin research and human genetics : the official journal of the International Society for Twin Studies.

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

K. Christensen, B. Maher, M. Marazita, 2004, The New England journal of medicine.

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

Nancy R. Downing, Janet K. Williams, M. Driessnack, 2013, Journal of Community Genetics.

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

Ana María López, R. T. Lie, A. Wilcox, 2009, Human molecular genetics.

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

E. Pugh, A. Jugessur, B. Maher, 2009, Human Heredity.

FOXE 1 association with both isolated cleft lip with or without cleft palate , and isolated cleft palate

Ana María López, R. T. Lie, A. Wilcox, 2009 .

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

T. Beaty, N. Prescott, R. Scott, 2004, American journal of human genetics.

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

R. Munger, C. Corcoran, S. Daack-Hirsch, 2004, Birth defects research. Part A, Clinical and molecular teratology.

Genetic Determinants of Facial Clefting: Analysis of 357 Candidate Genes Using Two National Cleft Studies from Scandinavia

Min Shi, Kaare Christensen, Camilla Bille, 2009, PloS one.

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.

R. Munger, J. Murray, T. Burns, 1999, Teratology.

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.

L. Ashworth, S. Patil, J. Murray, 1998, Genomics.

A Case of 3q29 Microdeletion Syndrome Involving Oral Cleft Inherited from a Nonaffected Mosaic Parent: Molecular Analysis and Ethical Implications

J. Murray, S. Daack-Hirsch, J. L'heureux, 2011, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

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

Nancy R. Downing, Janet K. Williams, M. Driessnack, 2013, Patient education and counseling.

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

Martha Driessnack, Janet K. Williams, M. Driessnack, 2012, Genetic testing and molecular biomarkers.

Beliefs on the causes of birth defects as perceived by mothers of children with birth defects in a tertiary care hospital in the Philippines

S. Daack-Hirsch, C. Padilla, M. Laurino, 2022, Journal of Community Genetics.

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

M. Marazita, J. Murray, S. Daack-Hirsch, 2008, American journal of medical genetics. Part A.

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

M. Marazita, S. Daack-Hirsch, A. Lidral, 2007, American journal of medical genetics. Part A.

Context for Filipino community based orofacial cleft prevention interventions

S. Daack-Hirsch, 2007 .

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

J. Rubenstein, T. Doetschman, J. Murray, 1998, American journal of human genetics.

Clinical and Epidemiologic Studies of Cleft up and Palate in the Philippines

K. Buetow, R. Munger, J. Murray, 1997 .

Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review

S. Daack-Hirsch, Lisa L. Shah, 2018, Journal of Genetic Counseling.

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

Kaitlyn A. Jones, M. Doerr, S. Daack-Hirsch, 2019, Health expectations : an international journal of public participation in health care and health policy.

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

S. Kondo, S. Bale, M. Vikkula, 2009, Genetics in Medicine.

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

M. Heitkemper, S. Henly, Y. Conley, 2015, Nursing outlook.

Establishing the Genomic Knowledge Matrix for Nursing Science

Mary Regan, Mary B. Engler, Bernice Coleman, 2018, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

Women's knowledge and use of prenatal screening tests

H. Skirton, M. Seven, S. Daack-Hirsch, 2017, Journal of clinical nursing.

A Closer Look at the Recommended Criteria for Disclosing Genetic Results: Perspectives of Medical Genetic Specialists, Genomic Researchers, and Institutional Review Board Chairs

Nancy R. Downing, Janet K. Williams, M. Driessnack, 2013, Journal of Genetic Counseling.

Informed Consent and Genomic Incidental Findings: IRB Chair Perspectives

Janet K. Williams, M. Driessnack, C. Simon, 2011, Journal of empirical research on human research ethics : JERHRE.

Filipino explanatory models of cleft lip with or without cleft palate.

S. Daack-Hirsch, Henrietta Gamboa, 2010, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

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

S. Campo, S. Daack-Hirsch, Lisa L. Shah, 2019, Research in nursing & health.

Filipino Explanatory Models of Cleft Lip with or without Cleft Palate

S. Daack-Hirsch, Henrietta Gamboa, 2010 .

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

K. Christensen, S. Daack-Hirsch, E. Castilla, 2006, American journal of medical genetics. Part A.

Communication about Congenital Adrenal Hyperplasia: Perspective of Filipino Families

S. Daack-Hirsch, C. Padilla, M. Laurino, 2017, Journal of Genetic Counseling.

Integrating genomics into undergraduate nursing education.

S. Daack-Hirsch, M. Quinn Griffin, Carla Dieter, 2011, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

Addressing the Decline in the Uptake of the Iowa Maternal and Prenatal Screening Program

J. Pendergast, E. Momany, S. Daack-Hirsch, 2017 .

Facilitators of and Barriers to Adherence to Dietary Interventions Perceived by Women With Multiple Sclerosis and Their Support Persons.

L. Snetselaar, S. Daack-Hirsch, T. Wahls, 2022, International journal of MS care.

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

R. Munger, J. Murray, T. Burns, 1998, European Journal of Epidemiology.

Bringing Personalized Medicine to a PACT Program: A Quality Improvement Project

S. Daack-Hirsch, V. Conley, Katie Halbmaier, 2020, Journal of the American Psychiatric Nurses Association.

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

S. Daack-Hirsch, B. Elder, C. A. Belchez, 2013, The Nursing clinics of North America.

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

S. Daack-Hirsch, C. Cunniff, Caleb C Holtzer, 2013, American journal of medical genetics. Part A.

A practical first step to integrating genetics into the curriculum.

M. Driessnack, Y. Perkhounkova, S. Daack-Hirsch, 2012, The Journal of nursing education.

The importance of patient engagement.

Janet K. Williams, M. Driessnack, C. Simon, 2013, Genetic testing and molecular biomarkers.

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

Janet K. Williams, M. Driessnack, S. Daack-Hirsch, 2013, Personalized medicine.

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

Y. Perkhounkova, S. Daack-Hirsch, Lisa L. Shah, 2016, Journal of Nursing Measurement.

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.

Min Shi, Kaare Christensen, Astanand Jugessur, 2011, Birth defects research. Part A, Clinical and molecular teratology.

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

Nicole M. Scott, S. Weinberg, K. Neiswanger, 2005, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Genetic counseling outcomes validation by genetics nurses in the UK and US.

M. Johnson, M. Maas, H. Skirton, 2001, Journal of Nursing Scholarship.

Coeliac disease in twins

R. Gorlin, S. Daack-Hirsch, J. V. Bokhoven, 2002, Journal of medical genetics.

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

S. Daack-Hirsch, C. Cunniff, Caleb C Holtzer, 2013, American journal of medical genetics. Part A.