Melissa A Parisi (Melissa Parisi)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 15

Top Topics

Health Information

Preterm Infants

Cognitive Decline

Top Venues

American journal of medical genetics. Part C, Seminars in medical genetics

American journal of medical genetics. Part A

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Sujata Bardhan, Huiqing Li, Erika Tarver, Charlene Schramm, Marishka Brown, Linda Garcia, Bryanna Schwartz, Anna Mazzucco, Nikila Natarajan, Elizabeth Walsh, Laurie Ryan, Gail Pearson, Melissa A Parisi
The National Institutes of Health INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan. American journal of medical genetics. Part C, Seminars in medical genetics 196 (1) (2024)
Sujata Bardhan, Huiqing Li, Erika Tarver, Charlene Schramm, Marishka Brown, Linda Garcia, Bryanna Schwartz, Anna Mazzucco, Nikila Natarajan, Elizabeth Walsh, Laurie Ryan, Gail Pearson, Melissa A Parisi
The National Institutes of Health INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan. American journal of medical genetics. Part C, Seminars in medical genetics 196 (1) (2024)
Sujata Bardhan, Huiqing Li, Erika Tarver, Charlene Schramm, Marishka Brown, Linda Garcia, Bryanna Schwartz, Anna Mazzucco, Nikila Natarajan, Elizabeth Walsh, Laurie Ryan, Gail Pearson, Melissa A Parisi
The National Institutes of Health INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan. American journal of medical genetics. Part C, Seminars in medical genetics 196 (1) (2024)
Sujata Bardhan, Huiqing Li, Erika Tarver, Charlene Schramm, Marishka Brown, Linda Garcia, Bryanna Schwartz, Anna Mazzucco, Nikila Natarajan, Elizabeth Walsh, Laurie Ryan, Gail Pearson, Melissa A Parisi
The National Institutes of Health INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan. American journal of medical genetics. Part C, Seminars in medical genetics 196 (1) (2024)
Sujata Bardhan, Huiqing Li, Erika Tarver, Charlene Schramm, Marishka Brown, Linda Garcia, Bryanna Schwartz, Anna Mazzucco, Nikila Natarajan, Elizabeth Walsh, Laurie Ryan, Gail Pearson, Melissa A Parisi
The National Institutes of Health INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan. American journal of medical genetics. Part C, Seminars in medical genetics (2024)
Philip John Brooks, Tiina K Urv, Melissa A Parisi
Gene-targeted therapies: Overview and implications. American journal of medical genetics. Part C, Seminars in medical genetics 193 (1) (2023)
Timothy W Yu, Stephen F Kingsmore, Robert C Green, Tippi MacKenzie, Melissa Wasserstein, Michele Caggana, Nina B Gold, Annie Kennedy, Priya S Kishnani, Matthew Might, Phillip J Brooks, Jill A Morris, Melissa A Parisi, Tiina K Urv
Are we prepared to deliver gene-targeted therapies for rare diseases? American journal of medical genetics. Part C, Seminars in medical genetics (2023)
Philip John Brooks, Tiina K Urv, Melissa A Parisi
Gene-targeted therapies: Overview and implications. American journal of medical genetics. Part C, Seminars in medical genetics (2023)
Melissa A Parisi, Michele Caggana, Jennifer L Cohen, Nina B Gold, Jill A Morris, Joseph J Orsini, Tiina K Urv, Melissa P Wasserstein
When is the best time to screen and evaluate for treatable genetic disorders?: A lifespan perspective. American journal of medical genetics. Part C, Seminars in medical genetics (2023)
Timothy W Yu, Stephen F Kingsmore, Robert C Green, Tippi MacKenzie, Melissa Wasserstein, Michele Caggana, Nina B Gold, Annie Kennedy, Priya S Kishnani, Matthew Might, Phillip J Brooks, Jill A Morris, Melissa A Parisi, Tiina K Urv
Are we prepared to deliver gene-targeted therapies for rare diseases? American journal of medical genetics. Part C, Seminars in medical genetics 193 (1) (2023)
Melissa A Parisi, Michele Caggana, Jennifer L Cohen, Nina B Gold, Jill A Morris, Joseph J Orsini, Tiina K Urv, Melissa P Wasserstein
When is the best time to screen and evaluate for treatable genetic disorders?: A lifespan perspective. American journal of medical genetics. Part C, Seminars in medical genetics 193 (1) (2023)
Mollie A Minear, Megan N Phillips, Alice Kau, Melissa A Parisi
Newborn screening research sponsored by the NIH: From diagnostic paradigms to precision therapeutics. American journal of medical genetics. Part C, Seminars in medical genetics 190 (2) (2022)
RaeLynn Forsyth, Melissa A Parisi, Burak Altintas, May Christine Malicdan, Thierry Vilboux, Jasmine Knoll, Brian P Brooks, Wadih M Zein, William A Gahl, Camilo Toro, Meral Gunay-Aygun
Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosis. American journal of medical genetics. Part C, Seminars in medical genetics 190 (1) (2022)
Jasmine Knoll, Burak Altintas, William A Gahl, Melissa A Parisi, Meral Gunay-Aygun
Growth in Joubert syndrome: Growth curves and physical measurements with correlation to genotype and hepatorenal disease in 170 individuals. American journal of medical genetics. Part A 188 (3) (2021)
Thierry Vilboux, Daniel A Doherty, Ian A Glass, Melissa A Parisi, Ian G Phelps, Andrew R Cullinane, Wadih Zein, Wadih M Zein, Theo Heller, Ariane G Soldatos, Neal L Oden, Deniz Yildirimli, Meghana Vemulapalli, James C Mullikin, null Nisc Comparative Sequencing Program, May Christine V Malicdan, William A Gahl, Meral Gunay-Aygun
Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center. Genetics in medicine : official journal of the American College of Medical Genetics 19 (8) (2017)