Michelle Primiano

Affiliations

Division of Clinical Genetics, Department of Pediatrics, New York Presbyterian Hospital, Columbia University, New York, NY, USA.

Réseau de co-auteurs

Priyanka Ahimaz 2 collaborations

Meredith Ross 2 collaborations

Kwame Anyane-Yeboa 2 collaborations

Jasmin Roohi 2 collaborations

Rebecca Hernan 1 collaboration

Megan T Cho 1 collaboration

Ashley L Wilson 1 collaboration

Catherine Au 1 collaboration

Sara M Berger 1 collaboration

Edwin Guzman 1 collaboration

Jessica E Shaw 1 collaboration

Leyla Tabanfar 1 collaboration

Ilana Chilton 1 collaboration

Emily Griffin 1 collaboration

Chana Ratner 1 collaboration

Alejandro Iglesias 1 collaboration

Laura Pisani 1 collaboration

Jimmy Duong 1 collaboration

Josue Martinez 1 collaboration

Paul Appelbaum 1 collaboration

Robert Klitzman 1 collaboration

Ruth Ottman 1 collaboration

Wendy K Chung 1 collaboration

Julia Wynn 1 collaboration

Muhammad Danyal Ahsan 1 collaboration

Isabelle R Chandler 1 collaboration

Samantha Min 1 collaboration

Benjamin Grant 1 collaboration

Jamieson Greenwald 1 collaboration

Tamar N Soussana 1 collaboration

Becky Baltich Nelson 1 collaboration

Charlene Thomas 1 collaboration

Eloise Chapman-Davis 1 collaboration

Ravi N Sharaf 1 collaboration

Melissa K Frey 1 collaboration

Mike Primiano 1 collaboration

Deb Sparks 1 collaboration

Jill Murphy 1 collaboration

Kathleen Glaser 1 collaboration

Molly McNett 1 collaboration

Emily P Solem 1 collaboration

Marshall P McQuillen 1 collaboration

Monika Zak Goelz 1 collaboration

Maria W A Teunissen 1 collaboration

Elly Lewerissa 1 collaboration

Eline J H van Hugte 1 collaboration

Shan Wang 1 collaboration

Charlotte W Ockeloen 1 collaboration

David A Koolen 1 collaboration

Rolph Pfundt 1 collaboration

Carlo L M Marcelis 1 collaboration

Eva Brilstra 1 collaboration

Jennifer L Howe 1 collaboration

Stephen W Scherer 1 collaboration

Xavier Le Guillou 1 collaboration

Frédéric Bilan 1 collaboration

Amelie Piton 1 collaboration

Anne de Saint Martin 1 collaboration

Sarah Baer 1 collaboration

Simone Seiffert 1 collaboration

Konrad Platzer 1 collaboration

Rami Abou Jamra 1 collaboration

Steffen Syrbe 1 collaboration

Jan H Doering 1 collaboration

Shenela Lakhani 1 collaboration

Srishti Nangia 1 collaboration

Christian Gilissen 1 collaboration

R Jeroen Vermeulen 1 collaboration

Rob P W Rouhl 1 collaboration

Han G Brunner 1 collaboration

Marjolein H Willemsen 1 collaboration

Nael Nadif Kasri 1 collaboration

Jennah Foltz 1 collaboration

Monisha Sebastin 1 collaboration

Ketki Naik 1 collaboration

Tamar Kramer 1 collaboration

Kelsie Bogyo 1 collaboration

Halie J May 1 collaboration

Jaehoon Jeong 1 collaboration

Anya Revah-Politi 1 collaboration

Julie S Cohen 1 collaboration

Anna Chassevent 1 collaboration

Julia Baptista 1 collaboration

Evan H Baugh 1 collaboration

Louise Bier 1 collaboration

Armand Bottani 1 collaboration

Maria Teresa Carminho A Rodrigues 1 collaboration

Charles Conlon 1 collaboration

Joel Fluss 1 collaboration

Michel Guipponi 1 collaboration

Chong Ae Kim 1 collaboration

Naomichi Matsumoto 1 collaboration

Richard Person 1 collaboration

Julia Rankin 1 collaboration

Marwan Shinawi 1 collaboration

Constance Smith-Hicks 1 collaboration

Aida Telegrafi 1 collaboration

Samantha Toy 1 collaboration

Yuri Uchiyama 1 collaboration

Vimla Aggarwal 1 collaboration

David B Goldstein 1 collaboration

Katherine W Roche 1 collaboration

Michelle Primiano

Affiliations

Publications (7)

Impact of patient education videos on genetic counseling outcomes after exome sequencing.

Uptake of Cascade Genetic Testing for Hereditary Breast and Ovarian Cancer: A Systematic Review and Meta-Analysis.

Using Radiofrequency Technology to Prevent Retained Sponges and Improve Patient Outcomes.

Factors associated with parental knowledge of neurofibromatosis type 1 (NF1): Parental affected status and genetic counseling.

ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.

Future Frontiers: Exploration of practices, challenges, and educational needs of genetic counselors in emerging subspecialties.

Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders.

Réseau de co-auteurs