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2011

Conference Publication

Complete Exome Sequencing for Marfan Syndrome, Osteogenesis Imperfecta and Stickler Syndrome: a New Era

McInerney-Leo, A., Glasov, E., Duncan, E. and Zankl, A. (2011). Complete Exome Sequencing for Marfan Syndrome, Osteogenesis Imperfecta and Stickler Syndrome: a New Era. Rheumatology Health Professionals Association 52nd Annual Scientific Meeting, Brisbane, Queensland, 14-17 May 2011. Richmond, VIC, Australia: Wiley-Blackwell. doi: 10.1111/j.1445-5994.2010.02467.x

Complete Exome Sequencing for Marfan Syndrome, Osteogenesis Imperfecta and Stickler Syndrome: a New Era

2007

Journal Article

Comprehensive screening of a north American Parkinson's disease cohort for LRRK2 mutation

Johnson, Janel, Paisan-Ruiz, Coro, Lopez, Grisel, Crews, Cynthia, Britton, Angela, Malkani, Roniel, Evans, E. Whitney, McInerney-Leo, Aideen, Jain, Shushant, Nussbaum, Robert L., Foote, Kelly D., Mandel, Ronald J., Crawley, Anthony, Reimsnider, Sharon, Fernandez, Hubert H., Okun, Michael S., Gwinn-Hardy, Katrina and Singleton, Andrew B. (2007). Comprehensive screening of a north American Parkinson's disease cohort for LRRK2 mutation. Neurodegenerative Diseases, 4 (5), 386-391. doi: 10.1159/000105160

Comprehensive screening of a north American Parkinson's disease cohort for LRRK2 mutation

2006

Journal Article

BRCA1/2 testing in hereditary breast and ovarian cancer families III: risk perception and screening

McInerney-Leo, Aideen, Hadley, Donald, Kase, Ronald G., Giambarresi, Therese R., Struewing, Jeffery P. and Biesecker, Barbara Bowles (2006). BRCA1/2 testing in hereditary breast and ovarian cancer families III: risk perception and screening. American Journal of Medical Genetics Part A, 140A (20), 2198-2206. doi: 10.1002/ajmg.a.31432

BRCA1/2 testing in hereditary breast and ovarian cancer families III: risk perception and screening

2006

Journal Article

Truth-telling and Turner syndrome: the importance of diagnostic disclosure

Sutton, Erica J., Young, Jessica, McInerney-Leo, Aideen, Bondy, Carolyn A., Gollust, Sarah E. and Biesecker, Barbara B. (2006). Truth-telling and Turner syndrome: the importance of diagnostic disclosure. Journal of Pediatrics, 148 (1), 102-107. doi: 10.1016/j.jpeds.2005.08.022

Truth-telling and Turner syndrome: the importance of diagnostic disclosure

2005

Journal Article

Turner syndrome: four challenges across the lifespan

Sutton, Erica J., McInerney-Leo, Aideen, Bondy, Carolyn A., Gollust, Sarah E., King, Donnice and Biesecker, Barbara (2005). Turner syndrome: four challenges across the lifespan. American Journal of Medical Genetics Part A, 139A (2), 57-66. doi: 10.1002/ajmg.a.30911

Turner syndrome: four challenges across the lifespan

2005

Journal Article

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

Simon-Sanchez, Javier, Hanson, Melissa, Singleton, Amanda, Hernandez, Dena, McInerney, Aideen, Nussbaum, Robert, Werner, John, Gallardo, Marisol, Weiser, Roberto, Gwinn-Hardy, Katrina, Singleton, Andrew B. and Clarimon, Jordi (2005). Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease. Neuroscience Letters, 382 (1-2), 191-194. doi: 10.1016/j.neulet.2005.03.015

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

2005

Journal Article

Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype

Meyer-Lindenberg, Andreas, Kohn, Philip D., Kolachana, Bhaskar, Kippenhan, Shane, McInerney-Leo, Aideen, Nussbaum, Robert, Weinberger, Daniel R. and Berman, Karen Faith (2005). Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype. Nature Neuroscience, 8 (5), 594-596. doi: 10.1038/nn1438

Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype

2005

Journal Article

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2

Hernandez, Dena G., Paisan-Ruiz, Coro, McInerney-Leo, Aideen, Jain, Shushant, Meyer-Lindenberg, Andreas, Evans, E. Whitney, Berman, Karen F., Johnson, Janel, Auburger, Georg, Schaffer, Alejandro A., Lopez, Grisel J., Nussbaum, Robert L. and Singleton, Andrew B. (2005). Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Annals of Neurology, 57 (3), 453-456. doi: 10.1002/ana.20401

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2

2005

Journal Article

BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships

McInerney‐Leo, Aideen, Biesecker, Barbara Bowles, Hadley, Donald W., Kase, Ronald G., Giambarresi, Therese R., Johnson, Elizabeth, Lerman, Caryn and Struewing, Jeffery P. (2005). BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships. American Journal of Medical Genetics Part A, 133A (2), 165-169. doi: 10.1002/ajmg.a.30566

BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships

2005

Journal Article

Genetic testing in Parkinson's disease

McInerney-Leo, Aideen, Hadley, Donald W., Gwinn-Hardy, Katrina and Hardy, John (2005). Genetic testing in Parkinson's disease. Movement Disorders, 20 (1), 1-10. doi: 10.1002/mds.20316

Genetic testing in Parkinson's disease

2005

Journal Article

Genetic testing in Parkinson's disease

McInerney-Leo, Aideen (2005). Genetic testing in Parkinson's disease. Movement Disorders, 20 (7), 908-909. doi: 10.1002/mds.20509

Genetic testing in Parkinson's disease

2004

Journal Article

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

Rogaeva, E., Johnson, J., Lang, A. E., Gulick, C., Gwinn-Hardy, K., Kawarai, T., Sato, C., Morgan, A., Werner, J., Nussbaum, R., Petit, A., Okun, M. S., McInerney, A., Mandel, R., Groen, J. L., Fernandez, H. H., Postuma, R., Foote, K. D., Salehi-Rad, S., Liang, Y., Reimsnider, S., Tandon, A., Hardy, J., St George-Hyslop, P. and Singleton, A. B. (2004). Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease. Archives of Neurology, 61 (12), 1898-1904. doi: 10.1001/archneur.61.12.1898

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

2004

Journal Article

Parkinsonism among Gaucher disease carriers

Goker-Alpan, O., Schiffmann, R., LaMarca, M.E., Nussbaum, R.L., McInerney-Leo, A. and Sidransky, E. (2004). Parkinsonism among Gaucher disease carriers. Journal of Medical Genetics, 41 (12), 937-940. doi: 10.1136/jmg.2004.024455

Parkinsonism among Gaucher disease carriers

2004

Journal Article

BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention

McInerney-Leo, Aideen, Biesecker, Barbara Bowles, Hadley, Donald W., Kase, Ronald G., Giambarresi, Therese R., Johnson, Elizabeth, Lerman, Caryn and Struewing, Jeffery P. (2004). BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention. American Journal of Medical Genetics Part A, 130A (3), 221-227. doi: 10.1002/ajmg.a.30265

BRCA1/2 testing in hereditary breast and ovarian cancer families: effectiveness of problem-solving training as a counseling intervention

2004

Journal Article

SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies

Johnson, J., Hague, S. M., Hanson, M., Gibson, A., Wilson, K. E., Evans, E. W., Singleton, A. A., McInerney-Leo, A., Nussbaum, R. L., Hernandez, D. G., Gallardo, M., McKeith, I. G., Burn, D. J., Ryu, M., Hellstrom, O., Ravina, B., Eerola, J., Perry, R. H., Jaros, E., Tienari, P., Weiser, R., Gwinn-Hardy, K., Morris, C. M., Hardy, J. and Singleton, A. B. (2004). SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies. Neurology, 63 (3), 554-556. doi: 10.1212/01.WNL.0000133401.09043.44

SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies

2004

Journal Article

Prevalence of Parkinson's disease in populations of African ancestry: a review

McInerney-Leo, Aideen, Gwinn-Hardy, Katrina and Nussbaum, Robert L. (2004). Prevalence of Parkinson's disease in populations of African ancestry: a review. Journal of the National Medical Association, 96 (7), 974-979.

Prevalence of Parkinson's disease in populations of African ancestry: a review

2001

Journal Article

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

Kelberman, D., Tyson, J., Chandler, D. C., McInerney, A. M., Slee, J., Albert, D., Aymat, A., Botma, M., Calvert, M., Goldblatt, J., Haan, E. A., Laing, N. G., Lim, J., Malcolm, S., Singer, S. L., Winter, R. M. and Bitner-Glindzicz, M. (2001). Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome. Human Genetics, 109 (6), 638-645. doi: 10.1007/s00439-001-0626-x

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

2001

Journal Article

An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility

Green, Michael J., Biesecker, Barbara B., McInerney, Aideen M., Mauger, David and Fost, Norman (2001). An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility. American Journal of Medical Genetics, 103 (1), 16-23. doi: 10.1002/ajmg.1500

An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility

2001

Journal Article

Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor

Green, Michael J., McInerney, Aideen M., Biesecker, Barbara B. and Fost, Norman (2001). Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor. American Journal of Medical Genetics, 103 (1), 24-31. doi: 10.1002/ajmg.1501

Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor

2000

Journal Article

Minocycline-induced generalized postinflammatory elastolysis

Ho, Nicola C, McInerney, Aideen, Levy, Howard, Francomano, Clair A and Elkayam, Ori (2000). Minocycline-induced generalized postinflammatory elastolysis. The American Journal of Medicine, 109 (4), 340-340. doi: 10.1016/s0002-9343(00)00499-x

Minocycline-induced generalized postinflammatory elastolysis