Irman Forghani

Affiliations

Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.

ORCID: 0000-0002-5484-5186

Publications (8)

Chimerism involving a RB1 pathogenic variant in monochorionic dizygotic twins with twin-twin transfusion syndrome.

American journal of medical genetics. Part A

Avec: Anna M Armitage , Monica A Kundra , Neda Ghiam , Paldeep S Atwal , Dayna Morel , Kathleen S Hruska , Rebecca Torene , J William Harbour , Irman Forghani

Prevalence of cardiovascular manifestations in patients with hypermobile Ehlers-Danlos syndrome at the University of Miami.

American journal of medical genetics. Part A

Avec: Jariselle M Pietri-Toro , Olivia K Gardner , Jessica D Leuchter , Gabrielle DiBartolomeo , Juanita A Hunter , Irman Forghani

Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome

Balkan medical journal

Avec: Irman Forghani

Application of the ACMG/NSGC genetic referral guidelines for hereditary renal cell carcinoma at the University of Miami, from 2014 to 2017.

American journal of medical genetics. Part A

Avec: Jessica D Leuchter , Priyen M Patel , Kayla M Fourzali , Talia R Donenberg , Rachel Silva-Smith , Nicolette C Vassallo , Susan H Blanton , Dipen J Parekh , Irman Forghani

First reported adult patient with retinal dystrophy and leukodystrophy caused by a novel ACBD5 variant: A case report and review of literature.

American journal of medical genetics. Part A

Avec: Michelle Bartlett , Nima Nasiri , Rena Pressman , Guney Bademci , Irman Forghani

EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder.

American journal of medical genetics. Part A

Avec: Irman Forghani , Steven H Lang , Matthew J Rodier , Stephanie A Bivona , Auteur inconnu , Alejo A Morales , Stephan Zuchner , Guney Bademci , Mustafa Tekin

Patient experiences of receiving a diagnosis of hypermobile Ehlers-Danlos syndrome.

American journal of medical genetics. Part A

Avec: Yun-Ting Wang , Shiva Jahani , Dayna Morel-Swols , Angelica Kapely , Ami Rosen , Irman Forghani

Poirier-Bienvenu neurodevelopmental syndrome: A report of a patient with a pathogenic variant in CSNK2B with abnormal linear growth.

American journal of medical genetics. Part A

Avec: Pavalan Selvam , Angita Jain , Anvir Cheema , Herjot Atwal , Irman Forghani , Paldeep S Atwal

Réseau de co-auteurs

Paldeep S Atwal 2 collaborations

Jessica D Leuchter 2 collaborations

Guney Bademci 2 collaborations

Anna M Armitage 1 collaboration

Monica A Kundra 1 collaboration

Neda Ghiam 1 collaboration

Dayna Morel 1 collaboration

Kathleen S Hruska 1 collaboration

Rebecca Torene 1 collaboration

J William Harbour 1 collaboration

Jariselle M Pietri-Toro 1 collaboration

Olivia K Gardner 1 collaboration

Gabrielle DiBartolomeo 1 collaboration

Juanita A Hunter 1 collaboration

Priyen M Patel 1 collaboration

Kayla M Fourzali 1 collaboration

Talia R Donenberg 1 collaboration

Rachel Silva-Smith 1 collaboration

Nicolette C Vassallo 1 collaboration

Susan H Blanton 1 collaboration

Dipen J Parekh 1 collaboration

Michelle Bartlett 1 collaboration

Nima Nasiri 1 collaboration

Rena Pressman 1 collaboration

Steven H Lang 1 collaboration

Matthew J Rodier 1 collaboration

Stephanie A Bivona 1 collaboration

None None 1 collaboration

Alejo A Morales 1 collaboration

Stephan Zuchner 1 collaboration

Mustafa Tekin 1 collaboration

Yun-Ting Wang 1 collaboration

Shiva Jahani 1 collaboration

Dayna Morel-Swols 1 collaboration

Angelica Kapely 1 collaboration

Ami Rosen 1 collaboration

Pavalan Selvam 1 collaboration

Angita Jain 1 collaboration

Anvir Cheema 1 collaboration

Herjot Atwal 1 collaboration