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{{short description|Iraqi geneticist}}
Professor Lihadh Al-Gazali MBChB MSc FRCP FRCPCH is a professor in clinical genetics and paediatrics. Her main area of interest is identifying new inherited disorders in Arab populations clinically and at the molecular level.
{{Infobox scientist

| image = <!--(filename only)-->

| birth_date = November 1950
Lihadh joined 200 people on 6th August 2016, in Montreal. On a reunion of her blood the family; Kubba family!
| birth_place = [[Amarah]], Iraq
She headed Stoning her cousin; that cousin was humiliated by Lihadh and her husband Wilma and her daughter Reem and her fake son in law Laith wail kubba. Then the very cousin was kicked out of the hotels dining area, kicked out of the reunion party and was deleted from all pictures taken and was moved out of the reunion video tape.
| death_date = <!--{{death date and age |YYYY|MM|DD |YYYY|MM|DD}}-->
| death_place =
| fields = Clinical genetics
| workplaces = Department of Paediatrics of [[United Arab Emirates University]]
| education = [[Iraqi University]], [[Baghdad Medical College]] (B.Med., B.Surg., 1973)
| known_for = Identifying inherited disorders in Arab populations
| awards = [[L'Oréal-UNESCO Award for Women in Science]]
}}
Professor '''Lihadh Al-Gazali''' MBChB MSc FRCP FRCPCH ({{Lang-ar|لحاظ الغزالي}}) is a professor in clinical genetics and paediatrics. Her main area of interest is identifying new inherited disorders in Arab populations clinically and at the molecular level.


==Biography==
==Biography==
Lihadh Al-Gazali was born and raised in [[Baghdad]], [[Iraq]].<ref name="Lancet">{{cite journal|last1=Shetty|first1=Priya|title=Lihadh Al-Gazali: a leading clinical geneticist in the Middle East|journal=The Lancet|date=March 2006|volume=367|issue=9515|pages=979|doi=10.1016/S0140-6736(06)68412-2|url=http://apps.elsevier.es/watermark/ctl_servlet?_f=10&pident_articulo=13174756&pident_usuario=0&pcontactid=&pident_revista=600&ty=61&accion=L&origen=zonadelectura&web=www.elsevier.es&lan=en&fichero=600v367n9515a13174756pdf001.pdf|pmid=16564349}}</ref> Her mother was an educationalist and her father an Army judge in Baghdad. She received higher education in UK.
Al-Gazali was born in November 1950 in [[Amarah]], [[Iraq]], and raised in Baghdad.<ref name="Lancet">{{cite journal|last1=Shetty|first1=Priya|title=Lihadh Al-Gazali: a leading clinical geneticist in the Middle East|journal=The Lancet|date=March 2006|volume=367|issue=9515|pages=979|doi=10.1016/S0140-6736(06)68412-2|url=http://apps.elsevier.es/watermark/ctl_servlet?_f=10&pident_articulo=13174756&pident_usuario=0&pcontactid=&pident_revista=600&ty=61&accion=L&origen=zonadelectura&web=www.elsevier.es&lan=en&fichero=600v367n9515a13174756pdf001.pdf|pmid=16564349|s2cid=36920215|access-date=2015-11-13|archive-url=https://web.archive.org/web/20151117021834/http://apps.elsevier.es/watermark/ctl_servlet?_f=10&pident_articulo=13174756&pident_usuario=0&pcontactid=&pident_revista=600&ty=61&accion=L&origen=zonadelectura&web=www.elsevier.es&lan=en&fichero=600v367n9515a13174756pdf001.pdf|archive-date=2015-11-17|url-status=dead}}</ref> Her mother was an educationalist and her father an Army judge in Baghdad. She received higher education in UK.{{fact|date=January 2020}}


Professor Al-Gazali studied medicine at the University of Iraq in Baghdad. She received her [[Bachelor of Medicine, Bachelor of Surgery]] from Baghdad Medical College in 1973. She married and had a child before moving to the United Kingdom in 1976 to study paediatrics and clinical genetics. She continued her education in Leeds and Edinburgh, living and practicing until 1990. She then moved to [[Al Ain]], becoming an assistant professor at the Department of Paediatrics of [[United Arab Emirates University]]. She played a key role in establishing the Centre for Arab Genomic Studies. In 1995 she set up the first registry for birth defects in the UAE. This registry was the first birth defects registry in an Arab country and the first to become a member of the International Clearing House of Birth Defects in Rome, Italy. She became an associate professor in 1997.<ref name="GN"/>
Al-Gazali studied medicine at the University of Iraq in Baghdad. She received her [[Bachelor of Medicine, Bachelor of Surgery]] from Baghdad Medical College in 1973. She married and had a child before moving to the United Kingdom in 1976 to study paediatrics and clinical genetics. She continued her education in Leeds and Edinburgh, living and practicing until 1990. She then moved to [[Al Ain]], becoming an assistant professor at the Department of Paediatrics of [[United Arab Emirates University]]. She played a role in establishing the Centre for Arab Genomic Studies. In 1995 she set up the first registry for birth defects in the UAE. This registry was the first birth defects registry in an Arab country and the first to become a member of the International Clearing House of Birth Defects in Rome, Italy. She became an associate professor in 1997.<ref name="GN"/>


She founded the first Clinical Genetics Service in the UAE, which offers support and counselling for families affected by congenital disorders. She has published over 240 scientific papers.
She founded the first Clinical Genetics Service in the UAE, which offers support and counselling for families affected by congenital disorders.{{fact|date=January 2020}} She has published over 240 scientific papers.{{fact|date=January 2020}}


Professor Al-Gazali received the Distinguished Performance Award in Research and Clinical Services of UAE University in 2003. In 2008 she received a [[L'Oréal-UNESCO Awards for Women in Science|L'Oréal-UNESCO Award for Women in Science]] "for her contributions to the characterization of inherited disorders."<ref name="GN" /> She also was awarded the [[Sheikh Hamdan bin Rashid Al Maktoum Award for Medical Sciences|Sheikh Hamdan Award]] for medical sciences which honours distinguished individuals working in medicine. In 2014 she was awarded the Takreem Award for Scientific and Technological achievement. In 2016, Professor Al-Gazali received the Abu Dhabi Award for service in clinical genetics and research.
Al-Gazali received the Distinguished Performance Award in Research and Clinical Services of UAE University in 2003. In 2008 she received a [[L'Oréal-UNESCO Awards for Women in Science|L'Oréal-UNESCO Award for Women in Science]] "for her contributions to the characterization of inherited disorders."<ref name="GN" /> She also was awarded the Sheikh Hamdan Award for medical sciences which honours distinguished individuals working in medicine. In 2014 she was awarded the Takreem Award for Scientific and Technological achievement. In 2016, Professor Al-Gazali received the Abu Dhabi Award for service in clinical genetics and research.{{fact|date=January 2020}}


==Personal life==
==Personal life==
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==Selected publications==
==Selected publications==
*{{cite journal|last1=Baasanjav|first1=Sevjidmaa|last2=Al-Gazali|first2=Lihadh|title=Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects|journal=The American Journal of Human Genetics|date=July 2011|volume=89|issue=1|pages=15–27|doi=10.1016/j.ajhg.2011.05.021|pmc=3135799|display-authors=etal|pmid=21763480}}
*{{cite journal|last1=Baasanjav|first1=Sevjidmaa|last2=Al-Gazali|first2=Lihadh|title=Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects|journal=The American Journal of Human Genetics|date=July 2011|volume=89|issue=1|pages=15–27|doi=10.1016/j.ajhg.2011.05.021|pmc=3135799|display-authors=etal|pmid=21763480}}
*{{cite journal|last1=Akawi|first1=NA|last2=Al-Gazali|first2=L|last3=Ali|first3=BR|title=Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations|journal=Clinical Genetics|date=August 2012|volume=82|issue=2|pages=147–156|doi=10.1111/j.1399-0004.2011.01734.x|pmid=21668896}}
*{{cite journal|last1=Akawi|first1=NA|last2=Al-Gazali|first2=L|last3=Ali|first3=BR|title=Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations|journal=Clinical Genetics|date=August 2012|volume=82|issue=2|pages=147–156|doi=10.1111/j.1399-0004.2011.01734.x|pmid=21668896|s2cid=23839531}}
*{{cite journal|last1=Al-Gazali|first1=Lihadh|last2=Walsh|first2=Christopher A.|title=A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts|journal=The American Journal of Human Genetics|date=December 2010|volume=87|issue=6|pages=882–889|doi=10.1016/j.ajhg.2010.10.026|pmid=21109224|pmc=2997371|display-authors=etal}}
*{{cite journal|last1=Al-Gazali|first1=Lihadh|last2=Walsh|first2=Christopher A.|title=A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts|journal=The American Journal of Human Genetics|date=December 2010|volume=87|issue=6|pages=882–889|doi=10.1016/j.ajhg.2010.10.026|pmid=21109224|pmc=2997371|display-authors=etal}}
*{{cite journal|last1=Al-Gazali|first1=L.|last2=Woods|first2=C. G.|title=A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy|journal=Journal of Medical Genetics|date=26 October 2010|volume=48|issue=2|pages=131–135|doi=10.1136/jmg.2010.081455|pmid=20978020|pmc=3030776}}
*{{cite journal|last1=Al-Gazali|first1=L.|last2=Woods|first2=C. G.|title=A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy|journal=Journal of Medical Genetics|date=26 October 2010|volume=48|issue=2|pages=131–135|doi=10.1136/jmg.2010.081455|pmid=20978020|pmc=3030776}}
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{{DEFAULTSORT:Gazali, Lihadh Al-}}
[[Category:Living people]]
[[Category:Living people]]
[[Category:Emirati scientists]]
[[Category:Emirati biologists]]
[[Category:Geneticists]]
[[Category:Emirati women scientists]]
[[Category:Iraqi scientists]]
[[Category:Iraqi geneticists]]
[[Category:Iraqi biologists]]
[[Category:Iraqi women scientists]]
[[Category:Iraqi women scientists]]
[[Category:People from Baghdad]]
[[Category:People from Baghdad]]
[[Category:United Arab Emirates University faculty]]
[[Category:Academic staff of United Arab Emirates University]]
[[Category:Women geneticists]]
[[Category:Women geneticists]]
[[Category:L'Oréal-UNESCO Awards for Women in Science laureates]]
[[Category:L'Oréal-UNESCO Awards for Women in Science laureates]]
[[Category:21st-century women scientists]]
[[Category:21st-century women scientists]]
[[Category:Year of birth missing (living people)]]

Latest revision as of 13:59, 14 April 2024

Lihadh Al-Gazali
BornNovember 1950
Amarah, Iraq
EducationIraqi University, Baghdad Medical College (B.Med., B.Surg., 1973)
Known forIdentifying inherited disorders in Arab populations
AwardsL'Oréal-UNESCO Award for Women in Science
Scientific career
FieldsClinical genetics
InstitutionsDepartment of Paediatrics of United Arab Emirates University

Professor Lihadh Al-Gazali MBChB MSc FRCP FRCPCH (Arabic: لحاظ الغزالي) is a professor in clinical genetics and paediatrics. Her main area of interest is identifying new inherited disorders in Arab populations clinically and at the molecular level.

Biography

[edit]

Al-Gazali was born in November 1950 in Amarah, Iraq, and raised in Baghdad.[1] Her mother was an educationalist and her father an Army judge in Baghdad. She received higher education in UK.[citation needed]

Al-Gazali studied medicine at the University of Iraq in Baghdad. She received her Bachelor of Medicine, Bachelor of Surgery from Baghdad Medical College in 1973. She married and had a child before moving to the United Kingdom in 1976 to study paediatrics and clinical genetics. She continued her education in Leeds and Edinburgh, living and practicing until 1990. She then moved to Al Ain, becoming an assistant professor at the Department of Paediatrics of United Arab Emirates University. She played a role in establishing the Centre for Arab Genomic Studies. In 1995 she set up the first registry for birth defects in the UAE. This registry was the first birth defects registry in an Arab country and the first to become a member of the International Clearing House of Birth Defects in Rome, Italy. She became an associate professor in 1997.[2]

She founded the first Clinical Genetics Service in the UAE, which offers support and counselling for families affected by congenital disorders.[citation needed] She has published over 240 scientific papers.[citation needed]

Al-Gazali received the Distinguished Performance Award in Research and Clinical Services of UAE University in 2003. In 2008 she received a L'Oréal-UNESCO Award for Women in Science "for her contributions to the characterization of inherited disorders."[2] She also was awarded the Sheikh Hamdan Award for medical sciences which honours distinguished individuals working in medicine. In 2014 she was awarded the Takreem Award for Scientific and Technological achievement. In 2016, Professor Al-Gazali received the Abu Dhabi Award for service in clinical genetics and research.[citation needed]

Personal life

[edit]

Professor Al-Gazali is married to Wessam Shather and has two daughters and a son.[2]

Selected publications

[edit]
  • Baasanjav, Sevjidmaa; Al-Gazali, Lihadh; et al. (July 2011). "Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects". The American Journal of Human Genetics. 89 (1): 15–27. doi:10.1016/j.ajhg.2011.05.021. PMC 3135799. PMID 21763480.
  • Akawi, NA; Al-Gazali, L; Ali, BR (August 2012). "Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations". Clinical Genetics. 82 (2): 147–156. doi:10.1111/j.1399-0004.2011.01734.x. PMID 21668896. S2CID 23839531.
  • Al-Gazali, Lihadh; Walsh, Christopher A.; et al. (December 2010). "A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts". The American Journal of Human Genetics. 87 (6): 882–889. doi:10.1016/j.ajhg.2010.10.026. PMC 2997371. PMID 21109224.
  • Al-Gazali, L.; Woods, C. G. (26 October 2010). "A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy". Journal of Medical Genetics. 48 (2): 131–135. doi:10.1136/jmg.2010.081455. PMC 3030776. PMID 20978020.

References

[edit]
  1. ^ Shetty, Priya (March 2006). "Lihadh Al-Gazali: a leading clinical geneticist in the Middle East" (PDF). The Lancet. 367 (9515): 979. doi:10.1016/S0140-6736(06)68412-2. PMID 16564349. S2CID 36920215. Archived from the original (PDF) on 2015-11-17. Retrieved 2015-11-13.
  2. ^ a b c Safvi, Talea (27 June 2008). "Lihadh Al Ghazali on genetics". Gulf News.