1.

Postdoctoral fellowship

ژن و سلول درماني, University of Texas Medical Branch, Galveston, Texas, USA, 1387-1384

2.

Postdoctoral fellowship

مد يكال ژنتيك- اپي ژنتيك, Baylor College of Medicine , Houston , Texas, USA , 1384-1382

3.

Postdoctoral fellowship

نوروژنتيك , دانشكده علوم پزشكي دانشگاه ناكازاكي ژاپن , 1382-1381

4.

MD

دكتراي تخصصي, دانشكده علوم پزشكي دانشگاه ناكازاكي ژاپن, 1381

5.

دكترا

دكتراي عمومي پزشكي, دانشكده پزشكي دانشگاه علوم پزشكي تهران, تهران, ايران, 1375

1.

American Society for Reproductive Endocrinology and Infertility Prize

July 2009,

2.

Society of Gynecology Investigation (SGI) President’s Presenter Awards

March 2009,

3.

Society of Gynecology Investigation (SGI) President’s Presenter Awards

March 2008,

4.

Best Presentation Award at the Annual Congress of Iranian PhD Students and Researchers

July 1999,

1.

Familial Ankyloglossia (Tongue-tie): A Case Report

Authors: Morowati S, Yasini M, Ranjbar R, Peivandi AA, Ghadami M
Acta Medica Iranica , Vol.48, No.2, Year. 2010, Page:124-123,

2.

Toward gene therapy of premature ovarian failure: intraovarian injection of adenovirus expressing human FSH receptor restores folliculogenesis in FSHR(-/-) FORKO mice

[pubmed]
Authors: Ghadami M, El-Demerdash E, Salama SA, Binhazim AA, Archibong AE, Chen X, Ballard BR, Sairam MR, Al-Hendy A
Mol Hum Reprod , Vol.16, No.4, Year. 2010, Page:241-50,

3.

Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type

Authors: Jain M, Wallis D, Robin NH, De Vrieze FW, Hardy JA, Ghadami M, Bosse K, Betz RC, Nöthen MM, Arcos-Burgos M, Muenke M
Am J Med Genet A, Vol.146A, No.17, Year. 2008, Page:2308-11,

4.

Toward gene therapy of primary ovarian failure: Adenovirus expressing human FSH receptor corrects the Finnish C566T mutation

Authors: Ghadami M, Salama A. S.Khatoon N, Chilvers R, Nagamani M, Chedrese J, and Al-Hendy A
Mol Hum Reprod , Vol.14, No.1, Year. 2008, Page:15-9,

5.

A single nucleotide polymorphism in the ABCC11 gene is the determinant of the human earwax type: Can we trace the road of ancient Mongoloid migration by this marker

Authors: Yoshiura K , Kinoshita A, Ishida T, Ninokata A, Ishikawa T, Kaname T, Bannai M, Tokunaga K, Sonoda S, Komaki R, Ihara M, Saenko V, Kaimovich AG, Sekine I, Komatsu K, Takahashi H, Nakashima M, Sosonkina N, Mapendano CK, Ghadami M, Nomura M, Linag D-S, Kim D-K, Garidkhuu A, Natsume N, Ohta T, Tomita H, Hirayama K, Ishibashi M, Takahashi A, Saito N, Saitou S, Nakamura Y, & Niikawa N
Nature Genet , Vol.38, No.3, Year. 2006, Page:324-30,

6.

Familial Isolated Congenital Anosmia With Morphologically Normal Olfactory Bulb in two Unrelated Iranian Families: A new Clinical Entity

Authors: Ghadami M, Majidzadeh-A K, Morovvati S, Damavandi E, Nishimura G, Kinoshita A, Komatsu K, Najafi M-T, Niikawa N, Yoshiura K-I
Am J Med Genet 127A, Year. 2004, Page:307– 309,

7.

Isolated Congenital Anosmia Locus Maps to 18p11.23-q12.2

Authors: Ghadami M, Morovvati S, Majidzadeh-A K, Damavandi E, Nishimura G, Kinoshita A, Pasalar P, Komatsu K, Najafi M-T, Niikawa N,Yoshiura K-I
J Med Genet, Vol.41, No.4, Year. 2004, Page:303-299,

8.

Confirmation of genetic homogeneity of non-syndromic low frequency sensorineural hearing loss by linkage analysis and DFNA6/14 mutations in a Japanese family

Authors: Komatsu K Nakamura N, Ghadami M, Matsumoto N, Kishino K, Ohta T, Niikawa N,Yoshiura K
J Hum Genet , Vol.47, Year. 2002, Page:395-399,

9.

The wet/dry earwax locus maps to chromosome 16p11.2-16q12.1

Authors: Tomita H-A, Yamada K, Ghadami M, Ogura T, Yanai Y, Nakatomi K, Sadamatsu M, Masui A, Nanko S, Kato N,Niikawa N
Lancet 359: 2000-02, Year. 2002,

10.

Camurati-Engelmann disease Type II: Progressive diaphyseal dysplasia with striations of the bones

Authors: Nishimura G, Nishimura H, Tanaka Y, Makita Y, Ikegawa S, Ghadami M, Kinoshita A,Niikawa N
Am J Med Genet 107, Year. 2002, Page:5-11,

11.

Two Thai families with Norrie disease (ND): Association of two novel missense mutations with severe ND phenotype, epileptic seizures, and manifesting female carrier

Authors: Yamada K, Limprasert P, Ratanasukon M, Tengtrisorn S, Yingchareonpukdee J, Vasiknanonte P, Kitaoka T, Ghadami M, Niikawa N,Kishino T
Am J Med Genet 100, Year. 2001, Page:52-55,

12.

Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family

Authors: Ghadami M, Majidzadeh-A K, Haerian B-S, Damavandi E, Yamada K, Pasalar P,Nishimura G, Tomita H-A, Yoshiura K,Niikawa N
Am J Med Genet 104, Year. 2001, Page:147-151,

13.

Bardet-Biedl syndrome type 3 in an Iranian family: Clinical study and confirmation of disease localization

Authors: Ghadami M, Tomita H-A, Najafi M-T, Yamada K, Majidzadeh-A K,Niikawa N
Am J Med Genet 94, Year. 2000, Page:433-437,

14.

Domain specific mutations in the human transforming growth factor beta 1 gene (TGFB1) result in Camurati-Engelmann disease

Authors: Kinoshita A, Tomita HA, Makita Y, Yoshida K, Ghadami M, Yamada K, Kondo S, Ikegawa S, Nishimura G, Fukushima Y, Murray JC, Niikawa N, Yoshiura K
Nature Genet 26, Year. 2000, Page:19-20,

15.

Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3

Authors: Ghadami M, Makita Y, Yoshida K, Fukushima Y, Wakui K, Ikegawa S, Yamada K, Kondo S, Niikawa N, Tomita H
Am J Hum Genet 66, Year. 2000, Page:147-143,

1.

Society Membership:American Society of Reproductive Medicine

Activity Type:Member

2.

Society Membership: American Society of Gene and Stem Cell Therap

Activity Type:Member

3.

Society Membership: American Society of Human Genetics

Activity Type:Member

4.

Society Membership: Japan Society of Human Genetics

Activity Type:Member

5.

Society Membership: Iranian Medical Council

Activity Type:Member

1. Stem Cell Therapy, Microarray and CGH

2. Epigenetics, Genetic linkage analysis, Genetic of Infertility, PGD, Medical Genetics, Gene therapy