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Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health.
Published in:
Journal of Personalized Medicine, 2018, v. 8, n. 3, p. 25, doi. 10.3390/jpm8030025
By:
- Sturm, Amy C.;
- Schmidlen, Tara;
- Scheinfeldt, Laura;
- Hovick, Shelly;
- McElroy, Joseph P.;
- Toland, Amanda E.;
- Roberts, J. Scott;
- Sweet, Kevin
Publication type:
Article
Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease.
Published in:
Journal of Personalized Medicine, 2014, v. 4, n. 1, p. 1, doi. 10.3390/jpm4010001
By:
- Sweet, Kevin;
- Gordon, Erynn S.;
- Sturm, Amy C.;
- Schmidlen, Tara J.;
- Manickam, Kandamurugu;
- Toland, Amanda Ewart;
- Keller, Margaret A.;
- Stack, Catharine B.;
- García-España, J. Felipe;
- Bellafante, Mark;
- Tayal, Neeraj;
- Embi, Peter;
- Binkley, Philip;
- Hershberger, Ray E.;
- Wolfgang Sadee;
- Christman, Michael;
- Marsh, Clay
Publication type:
Article
A Founder Mutation of the MSH2 Gene and Hereditary Nonpolyposis Colorectal Cancer in the United States.
Published in:
JAMA: Journal of the American Medical Association, 2004, v. 291, n. 6, p. 718, doi. 10.1001/jama.291.6.718
By:
- Lynch, Henry T.;
- Coronel, Stephanie M.;
- Okimoto, Ross;
- Hampel, Heather;
- Sweet, Kevin;
- Lynch, Jane F.;
- Barrows, Ali;
- Wijnen, Juul;
- van der Klift, Heleen;
- Franken, Patrick;
- Wagner, Anja;
- Fodde, Riccardo;
- de la Chapelle, Albert
Publication type:
Article
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
Published in:
Journal of Genetic Counseling, 2018, v. 27, n. 5, p. 1111, doi. 10.1007/s10897-018-0230-z
By:
- Schmidlen, Tara;
- Sturm, Amy C.;
- Hovick, Shelly;
- Scheinfeldt, Laura;
- Scott Roberts, J.;
- Morr, Lindsey;
- McElroy, Joseph;
- Toland, Amanda E.;
- Christman, Michael;
- O’Daniel, Julianne M.;
- Gordon, Erynn S.;
- Bernhardt, Barbara A.;
- Ormond, Kelly E.;
- Sweet, Kevin
Publication type:
Article
Book Review: Mass customization and design democratization.
Published in:
2020
By:
- Sweet, Kevin
Publication type:
Book Review
Concurrent germline BRCA1, BRCA2, and CHEK2 pathogenic variants in hereditary breast cancer: a case series.
Published in:
Breast Cancer Research & Treatment, 2021, v. 186, n. 2, p. 569, doi. 10.1007/s10549-021-06095-w
By:
- Sukumar, Jasmine;
- Kassem, Mahmoud;
- Agnese, Doreen;
- Pilarski, Robert;
- Ramaswamy, Bhuvaneswari;
- Sweet, Kevin;
- Sardesai, Sagar
Publication type:
Article
How Online Family History Tool Design and Message Content Impact User Perceptions: An Examination of Family HealthLink.
Published in:
Public Health Genomics, 2018, v. 21, n. 1/2, p. 53, doi. 10.1159/000493847
By:
- Thomas, Sarah N.;
- Hovick, Shelly R.;
- Tan, Naomi;
- Sturm, Amy C.;
- Sweet, Kevin
Publication type:
Article
CYP2D6 Genetic Variation and Beta-Blocker Maintenance Dose in Patients with Heart Failure.
Published in:
Pharmaceutical Research, 2017, v. 34, n. 8, p. 1615, doi. 10.1007/s11095-017-2104-8
By:
- Luzum, Jasmine;
- Sweet, Kevin;
- Binkley, Philip;
- Schmidlen, Tara;
- Jarvis, Joseph;
- Christman, Michael;
- Sadee, Wolfgang;
- Kitzmiller, Joseph
Publication type:
Article
Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study.
Published in:
International Journal of Colorectal Disease, 2010, v. 25, n. 6, p. 703, doi. 10.1007/s00384-010-0907-8
By:
- Buchanan, Daniel D.;
- Sweet, Kevin;
- Drini, Musa;
- Jenkins, Mark A.;
- Win, Aung Ko;
- Gattas, Michael;
- Walsh, Michael D.;
- Clendenning, Mark;
- McKeone, Diane;
- Walters, Rhiannon;
- Roberts, Aedan;
- Young, Alasdair;
- Hampel, Heather;
- Hopper, John L.;
- Goldblatt, Jack;
- George, Jill;
- Suthers, Graeme K.;
- Phillips, Kerry;
- Young, Graeme P.;
- Chow, Elizabeth
Publication type:
Article
Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.
Published in:
PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066705
By:
- Clendenning, Mark;
- Young, Joanne P.;
- Walsh, Michael D.;
- Woodall, Sonja;
- Arnold, Julie;
- Jenkins, Mark;
- Win, Aung Ko;
- Hopper, John L.;
- Sweet, Kevin;
- Gallinger, Steven;
- Rosty, Christophe;
- Parry, Susan;
- Buchanan, Daniel D.
Publication type:
Article
Highly penetrant hereditary cancer syndromes.
Published in:
Oncogene, 2004, v. 23, n. 38, p. 6445, doi. 10.1038/sj.onc.1207714
By:
- Nagy, Rebecca;
- Sweet, Kevin;
- Eng, Charis
Publication type:
Article
Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients.
Published in:
Cancers, 2022, v. 14, n. 10, p. 2426, doi. 10.3390/cancers14102426
By:
- Espinel, Whitney;
- Champine, Marjan;
- Hampel, Heather;
- Jeter, Joanne;
- Sweet, Kevin;
- Pilarski, Robert;
- Pearlman, Rachel;
- Shane, Kate;
- Brock, Pamela;
- Westman, Judith A.;
- Kipnis, Lindsay;
- Sotelo, Jilliane;
- Chittenden, Anu;
- Culver, Samantha;
- Stopfer, Jill E.;
- Schneider, Katherine A.;
- Sacca, Rosalba;
- Koeller, Diane R.;
- Gaonkar, Shraddha;
- Vaccari, Erica
Publication type:
Article
Characterization of BRCA1 ring finger variants of uncertain significance.
Published in:
Breast Cancer Research & Treatment, 2010, v. 119, n. 3, p. 737, doi. 10.1007/s10549-009-0438-6
By:
- Sweet, Kevin;
- Senter, Leigha;
- Pilarski, Robert;
- Wei, Lai;
- Toland, Amanda
Publication type:
Article
Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study.
Published in:
2010
By:
- Buchanan, Daniel;
- Sweet, Kevin;
- Drini, Musa;
- Jenkins, Mark;
- Win, Aung;
- Gattas, Michael;
- Walsh, Michael;
- Clendenning, Mark;
- McKeone, Diane;
- Walters, Rhiannon;
- Roberts, Aedan;
- Young, Alasdair;
- Hampel, Heather;
- Hopper, John;
- Goldblatt, Jack;
- George, Jill;
- Suthers, Graeme;
- Phillips, Kerry;
- Young, Graeme;
- Chow, Elizabeth
Publication type:
Correction Notice
Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis.
Published in:
JAMA: Journal of the American Medical Association, 2005, v. 294, n. 19, p. 2465, doi. 10.1001/jama.294.19.2465
By:
- Sweet, Kevin;
- Willis, Joseph;
- Zhou, Xiao-Ping;
- Gallione, Carol;
- Sawada, Takeshi;
- Alhopuro, Pia;
- Khoo, Sok Kean;
- Patocs, Attila;
- Martin, Cossette;
- Bridgeman, Scott;
- Heinz, John;
- Pilarski, Robert;
- Lehtonen, Rainer;
- Prior, Thomas W.;
- Frebourg, Thierry;
- Teh, Bin Tean;
- Marchuk, Douglas A.;
- Aaltonen, Lauri A.;
- Eng, Charis
Publication type:
Article
Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.
Published in:
Journal of Genetic Counseling, 2017, v. 26, n. 5, p. 980, doi. 10.1007/s10897-017-0073-z
By:
- Sweet, Kevin;
- Sturm, Amy;
- Schmidlen, Tara;
- McElroy, Joseph;
- Scheinfeldt, Laura;
- Manickam, Kandamurugu;
- Gordon, Erynn;
- Hovick, Shelly;
- Scott Roberts, J.;
- Toland, Amanda;
- Christman, Michael
Publication type:
Article
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
Published in:
Journal of Genetic Counseling, 2017, v. 26, n. 4, p. 738, doi. 10.1007/s10897-016-0044-9
By:
- Sweet, Kevin;
- Hovick, Shelly;
- Sturm, Amy;
- Schmidlen, Tara;
- Gordon, Erynn;
- Bernhardt, Barbara;
- Wawak, Lisa;
- Wernke, Karen;
- McElroy, Joseph;
- Scheinfeldt, Laura;
- Toland, Amanda;
- Roberts, J.;
- Christman, Michael
Publication type:
Article
Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative.
Published in:
Journal of Genetic Counseling, 2016, v. 25, n. 2, p. 385, doi. 10.1007/s10897-015-9883-z
By:
- Schmidlen, Tara;
- Scheinfeldt, Laura;
- Zhaoyang, Ruixue;
- Kasper, Rachel;
- Sweet, Kevin;
- Gordon, Erynn;
- Keller, Margaret;
- Stack, Cathy;
- Gharani, Neda;
- Daly, Mary;
- Jarvis, Joseph;
- Christman, Michael
Publication type:
Article
Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era.
Published in:
Journal of Genetic Counseling, 2014, v. 23, n. 4, p. 445, doi. 10.1007/s10897-014-9689-4
By:
- Hooker, Gillian;
- Ormond, Kelly;
- Sweet, Kevin;
- Biesecker, Barbara
Publication type:
Article
mTOR inhibitors reduce enteropathy, intestinal bleeding and colectomy rate in patients with juvenile polyposis of infancy with PTEN-BMPR1A deletion.
Published in:
Human Molecular Genetics, 2021, v. 30, n. 14, p. 1273, doi. 10.1093/hmg/ddab094
By:
- Taylor, Henry;
- Yerlioglu, Dilay;
- Phen, Claudia;
- Ballauff, Antje;
- Nedelkopoulou, Natalia;
- Spier, Isabel;
- Loverdos, Inés;
- Busoni, Veronica B;
- Heise, Jürgen;
- Dale, Peter;
- Meij, Tim de;
- Sweet, Kevin;
- Cohen, Marta C;
- Fox, Victor L;
- Mas, Emmanuel;
- Aretz, Stefan;
- Eng, Charis;
- Buderus, Stephan;
- Thomson, Mike;
- Rojas, Isabel
Publication type:
Article
The risk of breast cancer in women with a BRCA1 mutation from North America and Poland.
Published in:
International Journal of Cancer, 2012, v. 131, n. 1, p. 229, doi. 10.1002/ijc.26369
By:
- Lubinski, Jan;
- Huzarski, Tomasz;
- Byrski, Tomasz;
- Lynch, Henry T.;
- Cybulski, Cezary;
- Ghadirian, Parviz;
- Stawicka, Malgorzata;
- Foulkes, William D.;
- Kilar, Ewa;
- Kim-Sing, Charmaine;
- Neuhausen, Susan L.;
- Armel, Susan;
- Gilchrist, Dawna;
- Sweet, Kevin;
- Gronwald, Jacek;
- Eisen, Andrea;
- Gorski, Bohdan;
- Sun, Ping;
- Narod, Steven A.
Publication type:
Article
Methylation not a frequent “second hit” in tumors with germline BRCA mutations.
Published in:
Familial Cancer, 2009, v. 8, n. 4, p. 339, doi. 10.1007/s10689-009-9240-1
By:
- Dworkin, Amy;
- Spearman, Andrew;
- Tseng, Stephanie;
- Sweet, Kevin;
- Toland, Amanda
Publication type:
Article
Family History of Cancer and Cancer Risks in Women with BRCA1 or BRCA2 Mutations.
Published in:
JNCI: Journal of the National Cancer Institute, 2010, v. 102, n. 24, p. 1874, doi. 10.1093/jnci/djq443
By:
- Metcalfe, Kelly;
- Lubinski, Jan;
- Lynch, Henry T.;
- Ghadirian, Parviz;
- Foulkes, William D.;
- Kim-Sing, Charmaine;
- Neuhausen, Susan;
- Tung, Nadine;
- Rosen, Barry;
- Gronwald, Jacek;
- Ainsworth, Peter;
- Sweet, Kevin;
- Eisen, Andrea;
- Ping Sun;
- Narod, Steven A.
Publication type:
Article
Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?
Published in:
International Journal on Disability & Human Development (De Gruyter), 2001, v. 2, n. 3, p. 161, doi. 10.1515/ijdhd.2001.2.3.161
By:
- Sweet, Kevin;
- Martin, Edward;
- Eng, Charis;
- Shah, Manisha
Publication type:
Article
Cancer Risks for Relatives of Patients With Serrated Polyposis.
Published in:
American Journal of Gastroenterology (Springer Nature), 2012, v. 107, n. 5, p. 770, doi. 10.1038/ajg.2012.52
By:
- Win, Aung Ko;
- Walters, Rhiannon J;
- Buchanan, Daniel D;
- Jenkins, Mark A;
- Sweet, Kevin;
- Frankel, Wendy L;
- de la Chapelle, Albert;
- McKeone, Diane M;
- Walsh, Michael D;
- Clendenning, Mark;
- Pearson, Sally-Ann;
- Pavluk, Erika;
- Nagler, Belinda;
- Hopper, John L;
- Gattas, Michael R;
- Goldblatt, Jack;
- George, Jill;
- Suthers, Graeme K;
- Phillips, Kerry D;
- Woodall, Sonja
Publication type:
Article

Found: 25

Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health.

Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease.

A Founder Mutation of the MSH2 Gene and Hereditary Nonpolyposis Colorectal Cancer in the United States.

Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.

Book Review: Mass customization and design democratization.

Concurrent germline BRCA1, BRCA2, and CHEK2 pathogenic variants in hereditary breast cancer: a case series.

How Online Family History Tool Design and Message Content Impact User Perceptions: An Examination of Family HealthLink.

CYP2D6 Genetic Variation and Beta-Blocker Maintenance Dose in Patients with Heart Failure.

Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study.

Germline Mutations in the Polyposis-Associated Genes <i>BMPR1A</i>, <i>SMAD4, PTEN, MUTYH</i> and <i>GREM1</i> Are Not Common in Individuals with Serrated Polyposis Syndrome.

Highly penetrant hereditary cancer syndromes.

Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients.

Characterization of BRCA1 ring finger variants of uncertain significance.

Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study.

Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis.

Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.

Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.

Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative.

Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era.

mTOR inhibitors reduce enteropathy, intestinal bleeding and colectomy rate in patients with juvenile polyposis of infancy with PTEN-BMPR1A deletion.

The risk of breast cancer in women with a BRCA1 mutation from North America and Poland.

Methylation not a frequent “second hit” in tumors with germline BRCA mutations.

Family History of Cancer and Cancer Risks in Women with BRCA1 or BRCA2 Mutations.

Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?

Cancer Risks for Relatives of Patients With Serrated Polyposis.