Mohsen Fathzadeh is a Medical Geneticist and has 20+ years of experience in genomic science applications to advance health in diverse human populations. He conducted his Ph.D. thesis at Yale University, at Lab Prof Arya Mani, where he co-characterized a genetic form of familial Metabolic Syndrome. Since 2015, he has been a Postdoctoral Fellow at Stanford CV Med, Psychiatry, and PHS and eagerly conducting functional genomic analysis with mentorship from Professors Thomas Quertermous, Ruth O'Hara Drs. Joshua Knowles and David Rehkopf. Throughout collaboration with Merck & Co., Inc, he co-led identifying a gene regulator of body fat distribution and has been involved in characterizing several other insulin resistance and obesity-related genes. In his recent investigations, he analyzed the (epi)genetic link between newborn body fat distribution and high maternal gestational glucose levels in mother-child cohorts from multi-ethnic and deprived communities. He aims to leverage discoveries of genes and evolutionary pathways involved in regulating healthspan and age-related diseases and improve patients' lives. In his free time, Mohsen likes to go to the gym, swim and run, spend time with colleagues and learn about different cultures.

Honors & Awards

  • Stanford Global Health Seed Grant, Stanford University, Center for Innovation in Global Health (2020-2021)
  • Travel Award for Oral presentation, EAS (European Atherosclerosis Society) Glasgow, UK (2015)
  • Scholarship award for visiting Yale University, Digestive Disease Research Institute, TUMS (2012)
  • Nominated Oral Presentation, “Human Genetics Branch", 10th Iranian Genetics Congress, Iranian Genetics Society (2008)
  • Nominated for National Broadcasting interview, Channel 1, Young Researcher Award, ACECR, Fars Province Branch (2006)

Education & Certifications

  • Postdoctoral Fellowship, Stanford University, Cardiovascular Medicine/Cardiometabolic Genetic (2021)
  • Ph.D., Tehran University of Medical Sciences, Medical Genetics (2015)
  • Postgraduate, Yale University, Cardiovascular Genetics (2014)
  • MSc., Shahid Beheshti University, Human Genetics (2002)
  • BSc., Tehran University, Biology (1997)

Professional Affiliations and Activities

  • Reviewer, Elsevier, GENE (2014 - Present)
  • Reviewer, Archives of Iranian Medicine (AIM) Official journal of Academy of Medical Sciences of Iran) (2013 - Present)
  • Research Scientist, Digestive Dis. Research Institute, Tehran U Med Science (2012 - 2014)
  • Reviewer, Journal of Genetic Counseling (The National Society of Genetic Counselors, USA) (2008 - 2009)
  • Editorial Board, International Cardiovascular Res. Journal (ICRJ) (2007 - Present)
  • Research Scientist, Cardiovascular Research Center, Shiraz University of Medical Sciences (2007 - 2010)
  • Director, ACECR, Human Genetics Research Group, Shiraz (2002 - 2007)

All Publications

  • Dyrk1b promotes hepatic lipogenesis by bypassing canonical insulin signaling and directly activating mTORC2 in mice. The Journal of clinical investigation Bhat, N., Narayanan, A., Fathzadeh, M., Kahn, M., Zhang, D., Goedeke, L., Neogi, A., Cardone, R. L., Kibbey, R. G., Fernandez-Hernando, C., Ginsberg, H. N., Jain, D., Shulman, G., Mani, A. 2021


    Mutations in Dyrk1b are associated with metabolic syndrome and non-alcoholic fatty liver disease in humans. Our investigations showed that DYRK1B levels are increased in the liver of patients with non-alcoholic liver steatohepatitis (NASH) and in mice fed with a high fat/sucrose diet. Increasing Dyrk1b levels in the mouse liver enhanced de novo lipogenesis (DNL), fatty-acid uptake, and TAG secretion and caused NASH and hyperlipidemia. Conversely, knockdown of Dyrk1b was protective against high-calorie induced hepatic steatosis and fibrosis and hyperlipidemia. Mechanistically, Dyrk1b increased DNL by activating mTORC2 in a kinase independent fashion. Accordingly, the Dyrk1b-induced NASH was fully rescued when mTORC2 was genetically disrupted. The elevated DNL was associated with increased plasma membrane sn-1,2-diacylglyerol levels and increased PKCepsilon-mediated IRKT1150 phosphorylation, which resulted in impaired activation of hepatic insulin signaling and reduced hepatic glycogen storage. These findings provide new insights into the mechanisms that underlie Dyrk1b-induced hepatic lipogenesis and hepatic insulin resistance and identify Dyrk1b as a therapeutic target for NASH and insulin resistance in the liver.

    View details for DOI 10.1172/JCI153724

    View details for PubMedID 34855620

  • Dyrk1b promotes autophagy during skeletal muscle differentiation by upregulating 4e-bp1. Cellular signalling Bhat, N., Narayanan, A., Fathzadeh, M., Shah, K., Dianatpour, M., Abou Ziki, M. D., Mani, A. 2021: 110186


    Rare gain of function mutations in the gene encoding Dyrk1b, a key regulator of skeletal muscle differentiation, have been associated with sarcopenic obesity (SO) and metabolic syndrome (MetS) in humans. So far, the global gene networks regulated by Dyrk1b during myofiber differentiation have remained elusive. Here, we have performed untargeted proteomics to determine Dyrk1b-dependent gene-network in differentiated C2C12 myofibers. This analysis led to identification of translational inhibitor, 4e-bp1 as a post-transcriptional target of Dyrk1b in C2C12 cells. Accordingly, CRISPR/Cas9 mediated knockout of Dyrk1b in zebrafish identified 4e-bp1 as a downstream target of Dyrk1b in-vivo. The Dyrk1b knockout zebrafish embryos exhibited markedly reduced myosin heavy chain 1 expression in poorly developed myotomes and were embryonic lethal. Using knockdown and overexpression approaches in C2C12 cells, we found that 4e-bp1 enhances autophagy and mediates the effects of Dyrk1b on skeletal muscle differentiation. Dyrk1bR102C, the human sarcopenic obesity-associated mutation impaired muscle differentiation via excessive activation of 4e-bp1/autophagy axis in C2C12 cells. Strikingly, the defective muscle differentiation in Dyrk1bR102C cells was rescued by reduction of autophagic flux. The identification of Dyrk1b-4e-bp1-autophagy axis provides significant insight into pathways that are relevant to human skeletal muscle development and disorders.

    View details for DOI 10.1016/j.cellsig.2021.110186

    View details for PubMedID 34752933

  • Insulin Resistance and Mitochondrial Dysfunction Mediated by Nat1 Deficiency Sangwung, P., Fathzadeh, M., Knowles, J. AMER DIABETES ASSOC. 2020
  • FAM13A affects body fat distribution and adipocyte function. Nature communications Fathzadeh, M. n., Li, J. n., Rao, A. n., Cook, N. n., Chennamsetty, I. n., Seldin, M. n., Zhou, X. n., Sangwung, P. n., Gloudemans, M. J., Keller, M. n., Attie, A. n., Yang, J. n., Wabitsch, M. n., Carcamo-Orive, I. n., Tada, Y. n., Lusis, A. J., Shin, M. K., Molony, C. M., McLaughlin, T. n., Reaven, G. n., Montgomery, S. B., Reilly, D. n., Quertermous, T. n., Ingelsson, E. n., Knowles, J. W. 2020; 11 (1): 1465


    Genetic variation in the FAM13A (Family with Sequence Similarity 13 Member A) locus has been associated with several glycemic and metabolic traits in genome-wide association studies (GWAS). Here, we demonstrate that in humans, FAM13A alleles are associated with increased FAM13A expression in subcutaneous adipose tissue (SAT) and an insulin resistance-related phenotype (e.g. higher waist-to-hip ratio and fasting insulin levels, but lower body fat). In human adipocyte models, knockdown of FAM13A in preadipocytes accelerates adipocyte differentiation. In mice, Fam13a knockout (KO) have a lower visceral to subcutaneous fat (VAT/SAT) ratio after high-fat diet challenge, in comparison to their wild-type counterparts. Subcutaneous adipocytes in KO mice show a size distribution shift toward an increased number of smaller adipocytes, along with an improved adipogenic potential. Our results indicate that GWAS-associated variants within the FAM13A locus alter adipose FAM13A expression, which in turn, regulates adipocyte differentiation and contribute to changes in body fat distribution.

    View details for DOI 10.1038/s41467-020-15291-z

    View details for PubMedID 32193374

  • CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activation. Nature genetics Esteghamat, F. n., Broughton, J. S., Smith, E. n., Cardone, R. n., Tyagi, T. n., Guerra, M. n., Szabó, A. n., Ugwu, N. n., Mani, M. V., Azari, B. n., Kayingo, G. n., Chung, S. n., Fathzadeh, M. n., Weiss, E. n., Bender, J. n., Mane, S. n., Lifton, R. P., Adeniran, A. n., Nathanson, M. H., Gorelick, F. S., Hwa, J. n., Sahin-Tóth, M. n., Belfort-DeAguiar, R. n., Kibbey, R. G., Mani, A. n. 2019; 51 (8): 1233–43


    Factors that underlie the clustering of metabolic syndrome traits are not fully known. We performed whole-exome sequence analysis in kindreds with extreme phenotypes of early-onset atherosclerosis and metabolic syndrome, and identified novel loss-of-function mutations in the gene encoding the pancreatic elastase chymotrypsin-like elastase family member 2A (CELA2A). We further show that CELA2A is a circulating enzyme that reduces platelet hyperactivation, triggers both insulin secretion and degradation, and increases insulin sensitivity. CELA2A plasma levels rise postprandially and parallel insulin levels in humans. Loss of these functions by the mutant proteins provides insight into disease mechanisms and suggests that CELA2A could be an attractive therapeutic target.

    View details for DOI 10.1038/s41588-019-0470-3

    View details for PubMedID 31358993

    View details for PubMedCentralID PMC6675645

  • Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus Arteriosus. American journal of human genetics Li, N., Subrahmanyan, L., Smith, E., Yu, X., Zaidi, S., Choi, M., Mane, S., Nelson-Williams, C., Behjati, M., Kazemi, M., Hashemi, M., Fathzadeh, M., Narayanan, A., Tian, L., Montazeri, F., Mani, M., Begleiter, M. L., Coon, B. G., Lynch, H. T., Olson, E. N., Zhao, H., Ruland, J., Lifton, R. P., Mani, A. 2016; 99 (4): 1000-?

    View details for DOI 10.1016/j.ajhg.2016.09.003

    View details for PubMedID 27716515

    View details for PubMedCentralID PMC5065682

  • Nat1 Deficiency Is Associated with Mitochondrial Dysfunction and Exercise Intolerance in Mice CELL REPORTS Chennamsetty, I., Coronado, M., Contrepois, K., Keller, M. P., Carcamo-Orive, I., Sandin, J., Fajardo, G., Whittle, A. J., Fathzadeh, M., Snyder, M., Reaven, G., Attie, A. D., Bernstein, D., Quertermous, T., Knowles, J. W. 2016; 17 (2): 527-540


    We recently identified human N-acetyltransferase 2 (NAT2) as an insulin resistance (IR) gene. Here, we examine the cellular mechanism linking NAT2 to IR and find that Nat1 (mouse ortholog of NAT2) is co-regulated with key mitochondrial genes. RNAi-mediated silencing of Nat1 led to mitochondrial dysfunction characterized by increased intracellular reactive oxygen species and mitochondrial fragmentation as well as decreased mitochondrial membrane potential, biogenesis, mass, cellular respiration, and ATP generation. These effects were consistent in 3T3-L1 adipocytes, C2C12 myoblasts, and in tissues from Nat1-deficient mice, including white adipose tissue, heart, and skeletal muscle. Nat1-deficient mice had changes in plasma metabolites and lipids consistent with a decreased ability to utilize fats for energy and a decrease in basal metabolic rate and exercise capacity without altered thermogenesis. Collectively, our results suggest that Nat1 deficiency results in mitochondrial dysfunction, which may constitute a mechanistic link between this gene and IR.

    View details for DOI 10.1016/j.celrep.2016.09.005

    View details for Web of Science ID 000385850700019

    View details for PubMedID 27705799

    View details for PubMedCentralID PMC5097870

  • Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus Arteriosus AMERICAN JOURNAL OF HUMAN GENETICS Li, N., Subrahmanyan, L., Smith, E., Yu, X., Zaidi, S., Choi, M., Mane, S., Nelson-Williams, C., Bahjati, M., Kazemi, M., Hashemi, M., Fathzadeh, M., Narayanan, A., Tian, L., Montazeri, F., Mani, M., Begleiter, M. L., Coon, B. G., Lynch, H. T., Olson, E. N., Zhao, H., Ruland, J., Lifton, R. P., Mani, A. 2016; 98 (6): 1082–91


    Nonsyndromic patent ductus arteriosus (PDA) is a common congenital heart defect (CHD) with both inherited and acquired causes, but the disease mechanisms have remained elusive. Using combined genome-wide linkage analysis and whole-exome sequencing (WES), we identified independent mutations in PRDM6, which encodes a nuclear protein that is specific to vascular smooth muscle cells (VSMC), has histone methyl transferase activities, and acts as a transcriptional suppressor of contractile proteins. In vitro assays showed that the mutations cause loss of function either by intracellular redistribution of the protein and/or by alteration of its methyltransferase activities. Wild-type embryonic ductus arteriosus (DA) exhibited high levels of PRDM6, which rapidly declined postnatally as the number of VSMCs necessary for ductus contraction increased. This dynamic change suggests that PRDM6 plays a key role in maintaining VSMCs in an undifferentiated stage in order to promote their proliferation and that its loss of activity results in premature differentiation and impaired remodeling of the DA. Our findings identify PRDM6 mutations as underlying genetic causes of nonsyndromic isolated PDA in humans and implicates the wild-type protein in epigenetic regulation of ductus remodeling.

    View details for DOI 10.1016/j.ajhg.2016.03.022

    View details for Web of Science ID 000377286000004

    View details for PubMedID 27181681

    View details for PubMedCentralID PMC4908195

  • The Protective Effect of Transcription Factor 7-Like 2 Risk Allele rs7903146 against Elevated Fasting Plasma Triglyceride in Type 2 Diabetes: A Meta-Analysis JOURNAL OF DIABETES RESEARCH Wang, S., Song, K., Srivastava, R., Fathzadeh, M., Li, N., Mani, A. 2015


    The results from published studies regarding association of transcription factor 7-like 2 (TCF7L2) variant rs7903146 with dyslipidemia have been conflicting and inconclusive.We carried out a meta-analysis that aimed to investigate the association of the rs7903146 variant with plasma lipid levels using electronic database and published studies. Data was extracted by a standard algorithm. Dominant, recessive, homozygote, and heterozygote comparison models were utilized.24 studies incorporating 52,785 subjects were included in this meta-analysis. Overall, the minor allele (T) was associated with lower risk for hypertriglyceridemia in subjects with type 2 diabetes (dominant model: SMD = -0.04, 95% CI (-0.08, 0.00), P = 0.048, P heterogeneity = 0.47; recessive model: SMD = -0.10, 95% CI (-0.18, -0.02), P = 0.01, P heterogeneity = 0.56). No association was found between minor (T) allele and plasma TC, LDL-c, or HDL-c levels in subjects with type 2 diabetes or metabolic syndrome (MetS) and no association was found between minor (T) allele and plasma TG levels in nondiabetic subjects.Our meta-analysis indicated the association between TCF7L2 rs7903146 polymorphism and low plasma triglyceride (TG) level in subjects with type 2 diabetes. No association was found between rs7903146 variant and plasma lipids in nondiabetic subjects.

    View details for DOI 10.1155/2015/468627

    View details for Web of Science ID 000364845900001

    View details for PubMedID 26576435

    View details for PubMedCentralID PMC4631899

  • The metabolic syndrome and DYRK1B. New England journal of medicine Keramati, A. R., Fathzadeh, M., Mani, A. 2014; 371 (8): 785-786

    View details for DOI 10.1056/NEJMc1408235

    View details for PubMedID 25140972

  • The Metabolic Syndrome and DYRK1B NEW ENGLAND JOURNAL OF MEDICINE Morita, H., Komuro, I. 2014; 371 (8): 785

    View details for Web of Science ID 000340509900025

    View details for PubMedID 25140973

    View details for PubMedCentralID PMC4898778

  • A Form of the Metabolic Syndrome Associated with Mutations in DYRK1B NEW ENGLAND JOURNAL OF MEDICINE Keramati, A. R., Fathzadeh, M., Go, G., Singh, R., Choi, M., Faramarzi, S., Mane, S., Kasaei, M., Sarajzadeh-Fard, K., Hwa, J., Kidd, K. K., Bigi, M. A., Malekzadeh, R., Hosseinian, A., Babaei, M., Lifton, R. P., Mani, A. 2014; 370 (20): 1909-1919


    Genetic analysis has been successful in identifying causative mutations for individual cardiovascular risk factors. Success has been more limited in mapping susceptibility genes for clusters of cardiovascular risk traits, such as those in the metabolic syndrome.We identified three large families with coinheritance of early-onset coronary artery disease, central obesity, hypertension, and diabetes. We used linkage analysis and whole-exome sequencing to identify the disease-causing gene.A founder mutation was identified in DYRK1B, substituting cysteine for arginine at position 102 in the highly conserved kinase-like domain. The mutation precisely cosegregated with the clinical syndrome in all the affected family members and was absent in unaffected family members and unrelated controls. Functional characterization of the disease gene revealed that nonmutant protein encoded by DYRK1B inhibits the SHH (sonic hedgehog) and Wnt signaling pathways and consequently enhances adipogenesis. Furthermore, DYRK1B promoted the expression of the key gluconeogenic enzyme glucose-6-phosphatase. The R102C allele showed gain-of-function activities by potentiating these effects. A second mutation, substituting proline for histidine 90, was found to cosegregate with a similar clinical syndrome in an ethnically distinct family.These findings indicate a role for DYRK1B in adipogenesis and glucose homeostasis and associate its altered function with an inherited form of the metabolic syndrome. (Funded by the National Institutes of Health.).

    View details for DOI 10.1056/NEJMoa1301824

    View details for Web of Science ID 000336123600007

    View details for PubMedID 24827035

    View details for PubMedCentralID PMC4069260

  • Identification of a Novel Disease Gene for Early Onset Atherosclerosis, Diabetes and Metabolic Syndrome by Whole Exome Sequencing and Linkage Analysis Keramati, A. R., Fathzadeh, M., Singh, R., Choi, M., Faramarzi, S., Mane, S., Kasai, M., Bigib, M., Malekzadeh, R., Hosseinian, A., Babaie, M., Lifton, R., Mani, A. LIPPINCOTT WILLIAMS & WILKINS. 2013
  • Rare Nonconservative LRP6 Mutations Are Associated with Metabolic Syndrome HUMAN MUTATION Singh, R., Smith, E., Fathzadeh, M., Liu, W., Go, G., Subrahmanyan, L., Faramarzi, S., McKenna, W., Mani, A. 2013; 34 (9): 1221-1225


    A rare mutation in LRP6 has been shown to underlie autosomal dominant coronary artery disease (CAD) and metabolic syndrome in an Iranian kindred. The prevalence and spectrum of LRP6 mutations in the disease population of the United States is not known. Two hundred white Americans with early onset familial CAD and metabolic syndrome and 2,000 healthy Northern European controls were screened for nonconservative mutations in LRP6. Three novel mutations were identified, which cosegregated with the metabolic traits in the kindreds of the affected subjects and none in the controls. All three mutations reside in the second propeller domain, which plays a critical role in ligand binding. Two of the mutations substituted highly conserved arginines in the second YWTD domain and the third substituted a conserved glycosylation site. The functional characterization of one of the variants showed that it impairs Wnt signaling and acts as a loss of function mutation.

    View details for DOI 10.1002/humu.22360

    View details for Web of Science ID 000323109200007

    View details for PubMedID 23703864

    View details for PubMedCentralID PMC3745535

  • Epidemiological and clinical study of phenylketonuria (pku) disease in the national screening program of neonates Iranian Journal of Public Health Senemar, S., Ganjekarimi , H., Fathzadeh, M., Tarami , B., Bazrgar , M. 2009; 38 (2)
  • Apolipoprotein E polymorphism in Southern Iran: E4 allele in the lowest reported amounts MOLECULAR BIOLOGY REPORTS Bazrgar, M., Karimi, M., Fathzadeh, M., Senemar, S., Peiravian, F., Shojaee, A., Saadat, M. 2008; 35 (4): 495-499


    Apolipoprotein E (apoE) with three major alleles E2, E3 and E4 is one of the critical genes in lipid metabolism. Common apoE alleles are in association with an increase in risk for central nervous and cardiovascular diseases such as Alzheimer's disease, dementia, multiple sclerosis, atherosclerosis, coronary heart disease, hyperlipoproteinemia and stroke. ApoE3 is known as the most frequent allele in all populations, while association of apoE gene polymorphism with reported diseases have mostly been related to other two major alleles especially apoE4.To determine of apoE alleles frequencies in Southern Iran and comparison of those frequencies with other populations.DNA was extracted from the whole blood of 198 healthy unrelated candidates from population of Fars Province, Southern Iran, for apoE genotyping who were checked up by a physician. The frequencies of apoE alleles were compared with other populations by chi(2) test.The frequencies of E2, E3 and E4 were 0.063, 0.886 and 0.051 respectively. These values were similar to those reported from populations of Kuwait, Oman, Lebanon, India, Turkey, Greece, Spain, Sardinia Islands of Italy and two Iranian populations but were different from South of Italy and Caucasians in other Europe regions, American, American-Indian, African, East Asian and Saudi populations (P < 0.05).The frequency of E4 allele as a genetic risk factor for some multifactorial diseases in the population of Southern Iran is in the lowest reported amounts in the world. Iranian population has Caucasoid origin but differs from some Caucasian populations in Europe and America. The results of present study are in agreement with the historical evidences which show admixture of Iranian population with other populations and some studies based on genetic polymorphisms in the population of Southern Iran.

    View details for DOI 10.1007/s11033-007-9113-3

    View details for Web of Science ID 000261424100002

    View details for PubMedID 17594534

  • Genetic counseling in southern Iran: consanguinity and reason for referral. Journal of genetic counseling Fathzadeh, M., Babaie Bigi, M. A., Bazrgar, M., Yavarian, M., Tabatabaee, H. R., Akrami, S. M. 2008; 17 (5): 472-479


    Population based genetic counseling that promotes public health goals is an appropriate health care service. The genetic counseling center in Shiraz, southern Iran serves most of the clients in the region. During a 4-year period, 2,686 couples presented for genetic counseling. Data files revealed that 85% had consanguineous relationships (1.5% double first cousin, 74% first cousin, 8% second cousin, 1.5% beyond second cousin). Most prevalent reasons for referral were premarital counseling (80%), with 89% consanguinity, followed by preconception (12%), postnatal (7%), and prenatal counseling (1%). The most common abnormalities in probands or relatives were intellectual and developmental disabilities, hearing loss/impairment, and neuromuscular dystrophies. Family history of medical problem(s) and/or consanguinity was the main indication for referral in nearly every family. Premarital consanguinity poses unique challenges and opportunities. There is considerable opportunity for genetic counseling and education for couples in this population. The tradition of consanguinity, which is likely to persist in Iran, requires multidisciplinary agreement regarding the appropriate process of genetic counseling. Effective genetic counseling in Iran hinges on inclusion of data from genetic counseling services in national genomic and epidemiologic research programs.

    View details for DOI 10.1007/s10897-008-9163-2

    View details for PubMedID 18551360

  • Apolipoprotein E gene polymorphism and left ventricular function in Iranian patients with thalassemia major HAEMATOLOGICA-THE HEMATOLOGY JOURNAL Bazrgar, M., Karimi, M., Peiravian, F., Fathzadeh, M. 2007; 92 (2): 256-257


    Left ventricular (LV) failure is the main cause of death in thalassemia. Iron overload in patients with thalassemia leads to the formation of oxygen free radicals. Of the various apolipoprotein E (apoE) alleles, apoE4 is the least efficient in conditions of oxidative stress in comparison with apoE2 and apoE3. Our results showed that apoE4 is a genetic risk factor for LV dysfunction in thalassemia.

    View details for Web of Science ID 000244233600020

    View details for PubMedID 17296580

  • Impact of family history and consanguinity in severity of ‎mental retardation in children Annual Congress of Iranian Society of Pediatrics Fathzadeh, M., Senemar , S., Babaie , M. B. 2007
  • Frequency of cystathionine b-synthase 844ins 68 polymorphism in southern Iranian population Senemar, S., Fathzadeh, M., Bazrgar , M., Doroudgchi , M., Pezeshki , A., Ghaderi, A. 2007: 58–64
  • Frequency of 844ins68, cystathionine ‎ ‎- ‎synthase polymorphism as an anthropological marker to ‎diversity of southern Iran population from other ‎populations Archives of Iranian Medicine Senemar , S., Droudchi, M., Pezeshki, A., Bazrgar , M., Fathzadeh, M. 2007; 10 (4)
  • Epidemiological study of t4, t3 and tsh mean concentrations in four iranian populations Iranian Journal of Public Health Fathzadeh, M., Seyedna, Y., Khazali, H., Sheidai, M., Farhud, D. 2005; 34 (1): 74-79
  • Genetic and non-genetic disorders among progenies of consanguineous and unconsanguineous ‎marriages: Results from pedigrees of genetic counseling in Shiraz Journal of Medical Research Fathzadeh, M., Babaie , M., Bazrgar, M., Darboui, M., Shojaee, A. 2003; 3 (4): 95-100